Acid

From Wikipedia, the free encyclopedia

Zinc, a typical metal, reacting with hydrochloric acid, a typical acid

 

Acids and bases

An acid is a molecule or ion capable of either donating a proton (i.e. hydrogen ion, H⁺), known as a Brønsted–Lowry acid, or forming a covalent bond with an electron pair, known as a Lewis acid.

The first category of acids are the proton donors, or Brønsted–Lowry acids. In the special case of aqueous solutions, proton donors form the hydronium ion H₃O⁺ and are known as Arrhenius acids. Brønsted and Lowry generalized the Arrhenius theory to include non-aqueous solvents. A Brønsted or Arrhenius acid usually contains a hydrogen atom bonded to a chemical structure that is still energetically favorable after loss of H⁺.

Aqueous Arrhenius acids have characteristic properties that provide a practical description of an acid. Acids form aqueous solutions with a sour taste, can turn blue litmus red, and react with bases and certain metals (like calcium) to form salts. The word acid is derived from the Latin acidus, meaning 'sour'. An aqueous solution of an acid has a pH less than 7 and is colloquially also referred to as "acid" (as in "dissolved in acid"), while the strict definition refers only to the solute. A lower pH means a higher acidity, and thus a higher concentration of positive hydrogen ions in the solution. Chemicals or substances having the property of an acid are said to be acidic.

Common aqueous acids include hydrochloric acid (a solution of hydrogen chloride that is found in gastric acid in the stomach and activates digestive enzymes), acetic acid (vinegar is a dilute aqueous solution of this liquid), sulfuric acid (used in car batteries), and citric acid (found in citrus fruits). As these examples show, acids (in the colloquial sense) can be solutions or pure substances, and can be derived from acids (in the strict sense) that are solids, liquids, or gases. Strong acids and some concentrated weak acids are corrosive, but there are exceptions such as carboranes and boric acid.

The second category of acids are Lewis acids, which form a covalent bond with an electron pair. An example is boron trifluoride (BF₃), whose boron atom has a vacant orbital that can form a covalent bond by sharing a lone pair of electrons on an atom in a base, for example the nitrogen atom in ammonia (NH₃). Lewis considered this as a generalization of the Brønsted definition, so that an acid is a chemical species that accepts electron pairs either directly or by releasing protons (H⁺) into the solution, which then accept electron pairs. Hydrogen chloride, acetic acid, and most other Brønsted–Lowry acids cannot form a covalent bond with an electron pair, however, and are therefore not Lewis acids. Conversely, many Lewis acids are not Arrhenius or Brønsted–Lowry acids. In modern terminology, an acid is implicitly a Brønsted acid and not a Lewis acid, since chemists almost always refer to a Lewis acid explicitly as a Lewis acid.

Definitions and concepts

Main article: Acid–base reaction

Modern definitions are concerned with the fundamental chemical reactions common to all acids.

Most acids encountered in everyday life are aqueous solutions, or can be dissolved in water, so the Arrhenius and Brønsted–Lowry definitions are the most relevant.

The Brønsted–Lowry definition is the most widely used definition; unless otherwise specified, acid–base reactions are assumed to involve the transfer of a proton (H⁺) from an acid to a base.

Hydronium ions are acids according to all three definitions. Although alcohols and amines can be Brønsted–Lowry acids, they can also function as Lewis bases due to the lone pairs of electrons on their oxygen and nitrogen atoms.

Arrhenius acids

Svante Arrhenius

In 1884, Svante Arrhenius attributed the properties of acidity to hydrogen ions (H⁺), later described as protons or hydrons. An Arrhenius acid is a substance that, when added to water, increases the concentration of H⁺ ions in the water. Note that chemists often write H⁺(aq) and refer to the hydrogen ion when describing acid–base reactions but the free hydrogen nucleus, a proton, does not exist alone in water, it exists as the hydronium ion (H₃O⁺) or other forms (H₅O₂⁺, H₉O₄⁺). Thus, an Arrhenius acid can also be described as a substance that increases the concentration of hydronium ions when added to water. Examples include molecular substances such as hydrogen chloride and acetic acid.

An Arrhenius base, on the other hand, is a substance that increases the concentration of hydroxide (OH⁻) ions when dissolved in water. This decreases the concentration of hydronium because the ions react to form H₂O molecules:

H₃O⁺
_(aq) + OH⁻
_(aq) ⇌ H₂O_(liq) + H₂O_(liq)

Due to this equilibrium, any increase in the concentration of hydronium is accompanied by a decrease in the concentration of hydroxide. Thus, an Arrhenius acid could also be said to be one that decreases hydroxide concentration, while an Arrhenius base increases it.

In an acidic solution, the concentration of hydronium ions is greater than 10⁻⁷ moles per liter. Since pH is defined as the negative logarithm of the concentration of hydronium ions, acidic solutions thus have a pH of less than 7.

Brønsted–Lowry acids

Main article: Brønsted–Lowry acid–base theory

Acetic acid, a weak acid, donates a proton (hydrogen ion, highlighted in green) to water in an equilibrium reaction to give the acetate ion and the hydronium ion. Red: oxygen, black: carbon, white: hydrogen.

While the Arrhenius concept is useful for describing many reactions, it is also quite limited in its scope. In 1923, chemists Johannes Nicolaus Brønsted and Thomas Martin Lowry independently recognized that acid–base reactions involve the transfer of a proton. A Brønsted–Lowry acid (or simply Brønsted acid) is a species that donates a proton to a Brønsted–Lowry base. Brønsted–Lowry acid–base theory has several advantages over Arrhenius theory. Consider the following reactions of acetic acid (CH₃COOH), the organic acid that gives vinegar its characteristic taste:

CH₃COOH + H₂O ⇌ CH₃COO⁻ + H₃O⁺

CH₃COOH + NH₃ ⇌ CH₃COO⁻ + NH+4

Both theories easily describe the first reaction: CH₃COOH acts as an Arrhenius acid because it acts as a source of H₃O⁺ when dissolved in water, and it acts as a Brønsted acid by donating a proton to water. In the second example CH₃COOH undergoes the same transformation, in this case donating a proton to ammonia (NH₃), but does not relate to the Arrhenius definition of an acid because the reaction does not produce hydronium. Nevertheless, CH₃COOH is both an Arrhenius and a Brønsted–Lowry acid.

Brønsted–Lowry theory can be used to describe reactions of molecular compounds in nonaqueous solution or the gas phase. Hydrogen chloride (HCl) and ammonia combine under several different conditions to form ammonium chloride, NH₄Cl. In aqueous solution HCl behaves as hydrochloric acid and exists as hydronium and chloride ions. The following reactions illustrate the limitations of Arrhenius's definition:

1. H₃O⁺
   _(aq) + Cl⁻
   _(aq) + NH₃ → Cl⁻
   _(aq) + NH⁺
   _4(aq) + H₂O
2. HCl_(benzene) + NH_3(benzene) → NH₄Cl_(s)
3. HCl_(g) + NH_3(g) → NH₄Cl_(s)

As with the acetic acid reactions, both definitions work for the first example, where water is the solvent and hydronium ion is formed by the HCl solute. The next two reactions do not involve the formation of ions but are still proton-transfer reactions. In the second reaction hydrogen chloride and ammonia (dissolved in benzene) react to form solid ammonium chloride in a benzene solvent and in the third gaseous HCl and NH₃ combine to form the solid.

Lewis acids

Main article: Lewis acids and bases

A third, only marginally related concept was proposed in 1923 by Gilbert N. Lewis, which includes reactions with acid–base characteristics that do not involve a proton transfer. A Lewis acid is a species that accepts a pair of electrons from another species; in other words, it is an electron pair acceptor. Brønsted acid–base reactions are proton transfer reactions while Lewis acid–base reactions are electron pair transfers. Many Lewis acids are not Brønsted–Lowry acids. Contrast how the following reactions are described in terms of acid–base chemistry:

In the first reaction a fluoride ion, F⁻, gives up an electron pair to boron trifluoride to form the product tetrafluoroborate. Fluoride "loses" a pair of valence electrons because the electrons shared in the B—F bond are located in the region of space between the two atomic nuclei and are therefore more distant from the fluoride nucleus than they are in the lone fluoride ion. BF₃ is a Lewis acid because it accepts the electron pair from fluoride. This reaction cannot be described in terms of Brønsted theory because there is no proton transfer. The second reaction can be described using either theory. A proton is transferred from an unspecified Brønsted acid to ammonia, a Brønsted base; alternatively, ammonia acts as a Lewis base and transfers a lone pair of electrons to form a bond with a hydrogen ion. The species that gains the electron pair is the Lewis acid; for example, the oxygen atom in H₃O⁺ gains a pair of electrons when one of the H—O bonds is broken and the electrons shared in the bond become localized on oxygen. Depending on the context, a Lewis acid may also be described as an oxidizer or an electrophile. Organic Brønsted acids, such as acetic, citric, or oxalic acid, are not Lewis acids. They dissociate in water to produce a Lewis acid, H⁺, but at the same time also yield an equal amount of a Lewis base (acetate, citrate, or oxalate, respectively, for the acids mentioned). This article deals mostly with Brønsted acids rather than Lewis acids.

Dissociation and equilibrium

Reactions of acids are often generalized in the form HA ⇌ H⁺ + A⁻, where HA represents the acid and A⁻ is the conjugate base. This reaction is referred to as protolysis. The protonated form (HA) of an acid is also sometimes referred to as the free acid.

Acid–base conjugate pairs differ by one proton, and can be interconverted by the addition or removal of a proton (protonation and deprotonation, respectively). Note that the acid can be the charged species and the conjugate base can be neutral in which case the generalized reaction scheme could be written as HA⁺ ⇌ H⁺ + A. In solution there exists an equilibrium between the acid and its conjugate base. The equilibrium constant K is an expression of the equilibrium concentrations of the molecules or the ions in solution. Brackets indicate concentration, such that [H₂O] means the concentration of H₂O. The acid dissociation constant K_a is generally used in the context of acid–base reactions. The numerical value of K_a is equal to the product (multiplication) of the concentrations of the products divided by the concentration of the reactants, where the reactant is the acid (HA) and the products are the conjugate base and H⁺.

${\displaystyle K_a=\frac{[{\text{H}}^{+}][{\text{A}}^{-}]}{[\text{HA}]}}$

The stronger of two acids will have a higher K_a than the weaker acid; the ratio of hydrogen ions to acid will be higher for the stronger acid as the stronger acid has a greater tendency to lose its proton. Because the range of possible values for K_a spans many orders of magnitude, a more manageable constant, pK_a is more frequently used, where pK_a = −log₁₀ K_a. Stronger acids have a smaller pK_a than weaker acids. Experimentally determined pK_a at 25 °C in aqueous solution are often quoted in textbooks and reference material.

Nomenclature

Arrhenius acids are named according to their anions. In the classical naming system, the ionic suffix is dropped and replaced with a new suffix, according to the table following. The prefix "hydro-" is used when the acid is made up of just hydrogen and one other element. For example, HCl has chloride as its anion, so the hydro- prefix is used, and the -ide suffix makes the name take the form hydrochloric acid.

Classical naming system:

Anion prefix	Anion suffix	Acid prefix	Acid suffix	Example
per	ate	per	ic acid	perchloric acid (HClO4)
	ate		ic acid	chloric acid (HClO3)
	ite		ous acid	chlorous acid (HClO2)
hypo	ite	hypo	ous acid	hypochlorous acid (HClO)
	ide	hydro	ic acid	hydrochloric acid (HCl)

In the IUPAC naming system, "aqueous" is simply added to the name of the ionic compound. Thus, for hydrogen chloride, as an acid solution, the IUPAC name is aqueous hydrogen chloride.

Acid strength

Main article: Acid strength

The strength of an acid refers to its ability or tendency to lose a proton. A strong acid is one that completely dissociates in water; in other words, one mole of a strong acid HA dissolves in water yielding one mole of H⁺ and one mole of the conjugate base, A⁻, and none of the protonated acid HA. In contrast, a weak acid only partially dissociates and at equilibrium both the acid and the conjugate base are in solution. Examples of strong acids are hydrochloric acid (HCl), hydroiodic acid (HI), hydrobromic acid (HBr), perchloric acid (HClO₄), nitric acid (HNO₃) and sulfuric acid (H₂SO₄). In water each of these essentially ionizes 100%. The stronger an acid is, the more easily it loses a proton, H⁺. Two key factors that contribute to the ease of deprotonation are the polarity of the H—A bond and the size of atom A, which determines the strength of the H—A bond. Acid strengths are also often discussed in terms of the stability of the conjugate base.

Stronger acids have a larger acid dissociation constant, K_a and a more negative pK_a than weaker acids.

Sulfonic acids, which are organic oxyacids, are a class of strong acids. A common example is toluenesulfonic acid (tosylic acid). Unlike sulfuric acid itself, sulfonic acids can be solids. In fact, polystyrene functionalized into polystyrene sulfonate is a solid strongly acidic plastic that is filterable.

Superacids are acids stronger than 100% sulfuric acid. Examples of superacids are fluoroantimonic acid, magic acid, perchloric acid and Helium hydride. Superacids can permanently protonate water to give ionic, crystalline hydronium "salts". They can also quantitatively stabilize carbocations. In the case of Helium Hydride it would be especially strong due to the fact Helium is the least reactive noble gas. It would protonate anything it touched

While K_a measures the strength of an acid compound, the strength of an aqueous acid solution is measured by pH, which is an indication of the concentration of hydronium in the solution. The pH of a simple solution of an acid compound in water is determined by the dilution of the compound and the compound's K_a.

Lewis acid strength in non-aqueous solutions

Lewis acids have been classified in the ECW model and it has been shown that there is no one order of acid strengths. The relative acceptor strength of Lewis acids toward a series of bases, versus other Lewis acids, can be illustrated by C-B plots. It has been shown that to define the order of Lewis acid strength at least two properties must be considered. For Pearson's qualitative HSAB theory the two properties are hardness and strength while for Drago's quantitative ECW model the two properties are electrostatic and covalent.

Chemical characteristics

Monoprotic acids

See also: Acid dissociation constant § Monoprotic acids

Monoprotic acids, also known as monobasic acids, are those acids that are able to donate one proton per molecule during the process of dissociation (sometimes called ionization) as shown below (symbolized by HA):

HA (aq) + H₂O (l) ⇌ H₃O⁺ (aq) + A⁻ (aq)      K_a

Common examples of monoprotic acids in mineral acids include hydrochloric acid (HCl) and nitric acid (HNO₃). On the other hand, for organic acids the term mainly indicates the presence of one carboxylic acid group and sometimes these acids are known as monocarboxylic acid. Examples in organic acids include formic acid (HCOOH), acetic acid (CH₃COOH) and benzoic acid (C₆H₅COOH).

Polyprotic acids

See also: Acid dissociation constant § Polyprotic acids

Polyprotic acids, also known as polybasic acids, are able to donate more than one proton per acid molecule, in contrast to monoprotic acids that only donate one proton per molecule. Specific types of polyprotic acids have more specific names, such as diprotic (or dibasic) acid (two potential protons to donate), and triprotic (or tribasic) acid (three potential protons to donate). Some macromolecules such as proteins and nucleic acids can have a very large number of acidic protons.

A diprotic acid (here symbolized by H₂A) can undergo one or two dissociations depending on the pH. Each dissociation has its own dissociation constant, K_a1 and K_a2.

H₂A (aq) + H₂O (l) ⇌ H₃O⁺ (aq) + HA⁻ (aq)     K_a1

HA⁻ (aq) + H₂O (l) ⇌ H₃O⁺ (aq) + A²⁻ (aq)       K_a2

The first dissociation constant is typically greater than the second (i.e., K_a1 > K_a2). For example, sulfuric acid (H₂SO₄) can donate one proton to form the bisulfate anion (HSO⁻
₄), for which K_a1 is very large; then it can donate a second proton to form the sulfate anion (SO²⁻
₄), wherein the K_a2 is intermediate strength. The large K_a1 for the first dissociation makes sulfuric a strong acid. In a similar manner, the weak unstable carbonic acid (H₂CO₃) can lose one proton to form bicarbonate anion (HCO⁻
₃) and lose a second to form carbonate anion (CO²⁻
₃). Both K_a values are small, but K_a1 > K_a2 .

A triprotic acid (H₃A) can undergo one, two, or three dissociations and has three dissociation constants, where K_a1 > K_a2 > K_a3.

H₃A (aq) + H₂O (l) ⇌ H₃O⁺ (aq) + H₂A⁻ (aq)      K_a1

H₂A⁻ (aq) + H₂O (l) ⇌ H₃O⁺ (aq) + HA²⁻ (aq)       K_a2

HA²⁻ (aq) + H₂O (l) ⇌ H₃O⁺ (aq) + A³⁻ (aq)      K_a3

An inorganic example of a triprotic acid is orthophosphoric acid (H₃PO₄), usually just called phosphoric acid. All three protons can be successively lost to yield H₂PO⁻
₄, then HPO²⁻
₄, and finally PO³⁻
₄, the orthophosphate ion, usually just called phosphate. Even though the positions of the three protons on the original phosphoric acid molecule are equivalent, the successive K_a values differ since it is energetically less favorable to lose a proton if the conjugate base is more negatively charged. An organic example of a triprotic acid is citric acid, which can successively lose three protons to finally form the citrate ion.

Although the subsequent loss of each hydrogen ion is less favorable, all of the conjugate bases are present in solution. The fractional concentration, α (alpha), for each species can be calculated. For example, a generic diprotic acid will generate 3 species in solution: H₂A, HA⁻, and A²⁻. The fractional concentrations can be calculated as below when given either the pH (which can be converted to the [H⁺]) or the concentrations of the acid with all its conjugate bases:

${\displaystyle \begin{array}{rl}{\alpha }_{{\text{H}}_2^{}\text{A}}& =\frac{{[{\text{H}}^{+}]}^2}{{[{\text{H}}^{+}]}^2+[{\text{H}}^{+}]K_1+K_1{K}_2}=\frac{[{\text{H}}_2^{}\text{A}]}{[{\text{H}}_2^{}\text{A}]+[H{A}^{-}]+[A^{2-}]}\\ {\alpha }_{{\text{HA}}^{-}}& =\frac{[{\text{H}}^{+}]K_1}{{[{\text{H}}^{+}]}^2+[{\text{H}}^{+}]K_1+K_1{K}_2}=\frac{[\text{HA}-]}{[{\text{H}}_2^{}\text{A}]+[H{A}^{-}]+[A^{2-}]}\\ {\alpha }_{{\text{A}}^{2-}}& =\frac{K_1{K}_2}{{[{\text{H}}^{+}]}^2+[{\text{H}}^{+}]K_1+K_1{K}_2}=\frac{[{\text{A}}^{2-}]}{[{\text{H}}_2^{}\text{A}]+[H{A}^{-}]+[A^{2-}]}\end{array}}$

A plot of these fractional concentrations against pH, for given K₁ and K₂, is known as a Bjerrum plot. A pattern is observed in the above equations and can be expanded to the general n -protic acid that has been deprotonated i -times:

${\displaystyle {\alpha }_{{\text{H}}_{n-i}{A}^{i-}}=\frac{[{\text{H}}^{+}{]}^{n-i}{\displaystyle \prod _{j=0}^i{K}_j}}{{\displaystyle \sum _{i=0}^n[[{\text{H}}^{+}{]}^{n-i}{\displaystyle \prod _{j=0}^i{K}_j}}]}}$

where K₀ = 1 and the other K-terms are the dissociation constants for the acid.

Neutralization

Hydrochloric acid (in beaker) reacting with ammonia fumes to produce ammonium chloride (white smoke).

Neutralization is the reaction between an acid and a base, producing a salt and neutralized base; for example, hydrochloric acid and sodium hydroxide form sodium chloride and water:

HCl_(aq) + NaOH_(aq) → H₂O_(l) + NaCl_(aq)

Neutralization is the basis of titration, where a pH indicator shows equivalence point when the equivalent number of moles of a base have been added to an acid. It is often wrongly assumed that neutralization should result in a solution with pH 7.0, which is only the case with similar acid and base strengths during a reaction.

Neutralization with a base weaker than the acid results in a weakly acidic salt. An example is the weakly acidic ammonium chloride, which is produced from the strong acid hydrogen chloride and the weak base ammonia. Conversely, neutralizing a weak acid with a strong base gives a weakly basic salt (e.g., sodium fluoride from hydrogen fluoride and sodium hydroxide).

Weak acid–weak base equilibrium

Main article: Henderson–Hasselbalch equation

In order for a protonated acid to lose a proton, the pH of the system must rise above the pK_a of the acid. The decreased concentration of H⁺ in that basic solution shifts the equilibrium towards the conjugate base form (the deprotonated form of the acid). In lower-pH (more acidic) solutions, there is a high enough H⁺ concentration in the solution to cause the acid to remain in its protonated form.

Solutions of weak acids and salts of their conjugate bases form buffer solutions.

Titration

Main article: Acid–base titration

To determine the concentration of an acid in an aqueous solution, an acid–base titration is commonly performed. A strong base solution with a known concentration, usually NaOH or KOH, is added to neutralize the acid solution according to the color change of the indicator with the amount of base added. The titration curve of an acid titrated by a base has two axes, with the base volume on the x-axis and the solution's pH value on the y-axis. The pH of the solution always goes up as the base is added to the solution.

Example: Diprotic acid

This is an ideal titration curve for alanine, a diprotic amino acid. Point 2 is the first equivalent point where the amount of NaOH added equals the amount of alanine in the original solution.

For each diprotic acid titration curve, from left to right, there are two midpoints, two equivalence points, and two buffer regions.

Equivalence points

Due to the successive dissociation processes, there are two equivalence points in the titration curve of a diprotic acid. The first equivalence point occurs when all first hydrogen ions from the first ionization are titrated. In other words, the amount of OH⁻ added equals the original amount of H₂A at the first equivalence point. The second equivalence point occurs when all hydrogen ions are titrated. Therefore, the amount of OH⁻ added equals twice the amount of H₂A at this time. For a weak diprotic acid titrated by a strong base, the second equivalence point must occur at pH above 7 due to the hydrolysis of the resulted salts in the solution. At either equivalence point, adding a drop of base will cause the steepest rise of the pH value in the system.

Buffer regions and midpoints

A titration curve for a diprotic acid contains two midpoints where pH=pK_a. Since there are two different K_a values, the first midpoint occurs at pH=pK_a1 and the second one occurs at pH=pK_a2. Each segment of the curve that contains a midpoint at its center is called the buffer region. Because the buffer regions consist of the acid and its conjugate base, it can resist pH changes when base is added until the next equivalent points.

Applications of acids

In industry

Acids are fundamental reagents in treating almost all processes in modern industry. Sulfuric acid, a diprotic acid, is the most widely used acid in industry, and is also the most-produced industrial chemical in the world. It is mainly used in producing fertilizer, detergent, batteries and dyes, as well as used in processing many products such like removing impurities. According to the statistics data in 2011, the annual production of sulfuric acid was around 200 million tonnes in the world. For example, phosphate minerals react with sulfuric acid to produce phosphoric acid for the production of phosphate fertilizers, and zinc is produced by dissolving zinc oxide into sulfuric acid, purifying the solution and electrowinning.

In the chemical industry, acids react in neutralization reactions to produce salts. For example, nitric acid reacts with ammonia to produce ammonium nitrate, a fertilizer. Additionally, carboxylic acids can be esterified with alcohols, to produce esters.

Acids are often used to remove rust and other corrosion from metals in a process known as pickling. They may be used as an electrolyte in a wet cell battery, such as sulfuric acid in a car battery.

In food

Carbonated water (H₂CO₃ aqueous solution) is commonly added to soft drinks to make them effervesce.

Tartaric acid is an important component of some commonly used foods like unripened mangoes and tamarind. Natural fruits and vegetables also contain acids. Citric acid is present in oranges, lemon and other citrus fruits. Oxalic acid is present in tomatoes, spinach, and especially in carambola and rhubarb; rhubarb leaves and unripe carambolas are toxic because of high concentrations of oxalic acid. Ascorbic acid (Vitamin C) is an essential vitamin for the human body and is present in such foods as amla (Indian gooseberry), lemon, citrus fruits, and guava.

Many acids can be found in various kinds of food as additives, as they alter their taste and serve as preservatives. Phosphoric acid, for example, is a component of cola drinks. Acetic acid is used in day-to-day life as vinegar. Citric acid is used as a preservative in sauces and pickles.

Carbonic acid is one of the most common acid additives that are widely added in soft drinks. During the manufacturing process, CO₂ is usually pressurized to dissolve in these drinks to generate carbonic acid. Carbonic acid is very unstable and tends to decompose into water and CO₂ at room temperature and pressure. Therefore, when bottles or cans of these kinds of soft drinks are opened, the soft drinks fizz and effervesce as CO₂ bubbles come out.

Certain acids are used as drugs. Acetylsalicylic acid (Aspirin) is used as a pain killer and for bringing down fevers.

In human bodies

Acids play important roles in the human body. The hydrochloric acid present in the stomach aids digestion by breaking down large and complex food molecules. Amino acids are required for synthesis of proteins required for growth and repair of body tissues. Fatty acids are also required for growth and repair of body tissues. Nucleic acids are important for the manufacturing of DNA and RNA and transmitting of traits to offspring through genes. Carbonic acid is important for maintenance of pH equilibrium in the body.

Human bodies contain a variety of organic and inorganic compounds, among those dicarboxylic acids play an essential role in many biological behaviors. Many of those acids are amino acids, which mainly serve as materials for the synthesis of proteins. Other weak acids serve as buffers with their conjugate bases to keep the body's pH from undergoing large scale changes that would be harmful to cells. The rest of the dicarboxylic acids also participate in the synthesis of various biologically important compounds in human bodies.

Acid catalysis

Main article: Acid catalysis

Acids are used as catalysts in industrial and organic chemistry; for example, sulfuric acid is used in very large quantities in the alkylation process to produce gasoline. Some acids, such as sulfuric, phosphoric, and hydrochloric acids, also effect dehydration and condensation reactions. In biochemistry, many enzymes employ acid catalysis.

Biological occurrence

Basic structure of an amino acid.

Many biologically important molecules are acids. Nucleic acids, which contain acidic phosphate groups, include DNA and RNA. Nucleic acids contain the genetic code that determines many of an organism's characteristics, and is passed from parents to offspring. DNA contains the chemical blueprint for the synthesis of proteins, which are made up of amino acid subunits. Cell membranes contain fatty acid esters such as phospholipids.

An α-amino acid has a central carbon (the α or alpha carbon) that is covalently bonded to a carboxyl group (thus they are carboxylic acids), an amino group, a hydrogen atom and a variable group. The variable group, also called the R group or side chain, determines the identity and many of the properties of a specific amino acid. In glycine, the simplest amino acid, the R group is a hydrogen atom, but in all other amino acids it is contains one or more carbon atoms bonded to hydrogens, and may contain other elements such as sulfur, oxygen or nitrogen. With the exception of glycine, naturally occurring amino acids are chiral and almost invariably occur in the L-configuration. Peptidoglycan, found in some bacterial cell walls contains some D-amino acids. At physiological pH, typically around 7, free amino acids exist in a charged form, where the acidic carboxyl group (-COOH) loses a proton (-COO⁻) and the basic amine group (-NH₂) gains a proton (-NH⁺
₃). The entire molecule has a net neutral charge and is a zwitterion, with the exception of amino acids with basic or acidic side chains. Aspartic acid, for example, possesses one protonated amine and two deprotonated carboxyl groups, for a net charge of −1 at physiological pH.

Fatty acids and fatty acid derivatives are another group of carboxylic acids that play a significant role in biology. These contain long hydrocarbon chains and a carboxylic acid group on one end. The cell membrane of nearly all organisms is primarily made up of a phospholipid bilayer, a micelle of hydrophobic fatty acid esters with polar, hydrophilic phosphate "head" groups. Membranes contain additional components, some of which can participate in acid–base reactions.

In humans and many other animals, hydrochloric acid is a part of the gastric acid secreted within the stomach to help hydrolyze proteins and polysaccharides, as well as converting the inactive pro-enzyme, pepsinogen into the enzyme, pepsin. Some organisms produce acids for defense; for example, ants produce formic acid.

Acid–base equilibrium plays a critical role in regulating mammalian breathing. Oxygen gas (O₂) drives cellular respiration, the process by which animals release the chemical potential energy stored in food, producing carbon dioxide (CO₂) as a byproduct. Oxygen and carbon dioxide are exchanged in the lungs, and the body responds to changing energy demands by adjusting the rate of ventilation. For example, during periods of exertion the body rapidly breaks down stored carbohydrates and fat, releasing CO₂ into the blood stream. In aqueous solutions such as blood CO₂ exists in equilibrium with carbonic acid and bicarbonate ion.

CO₂ + H₂O ⇌ H₂CO₃ ⇌ H⁺ + HCO−3

It is the decrease in pH that signals the brain to breathe faster and deeper, expelling the excess CO₂ and resupplying the cells with O₂.

Aspirin (acetylsalicylic acid) is a carboxylic acid

Cell membranes are generally impermeable to charged or large, polar molecules because of the lipophilic fatty acyl chains comprising their interior. Many biologically important molecules, including a number of pharmaceutical agents, are organic weak acids that can cross the membrane in their protonated, uncharged form but not in their charged form (i.e., as the conjugate base). For this reason the activity of many drugs can be enhanced or inhibited by the use of antacids or acidic foods. The charged form, however, is often more soluble in blood and cytosol, both aqueous environments. When the extracellular environment is more acidic than the neutral pH within the cell, certain acids will exist in their neutral form and will be membrane soluble, allowing them to cross the phospholipid bilayer. Acids that lose a proton at the intracellular pH will exist in their soluble, charged form and are thus able to diffuse through the cytosol to their target. Ibuprofen, aspirin and penicillin are examples of drugs that are weak acids.

Common acids

Mineral acids (inorganic acids)

• Hydrogen halides and their solutions: hydrofluoric acid (HF), hydrochloric acid (HCl), hydrobromic acid (HBr), hydroiodic acid (HI)
• Halogen oxoacids: hypochlorous acid (HClO), chlorous acid (HClO₂), chloric acid (HClO₃), perchloric acid (HClO₄), and corresponding analogs for bromine and iodine
  • Hypofluorous acid (HFO), the only known oxoacid for fluorine.
• Sulfuric acid (H₂SO₄)
• Fluorosulfuric acid (HSO₃F)
• Nitric acid (HNO₃)
• Phosphoric acid (H₃PO₄)
• Fluoroboric acid (HBF₄)
• Hexafluorophosphoric acid (HPF₆)
• Chromic acid (H₂CrO₄)
• Boric acid (H₃BO₃)

Sulfonic acids

A sulfonic acid has the general formula RS(=O)₂–OH, where R is an organic radical.

• Methanesulfonic acid (or mesylic acid, CH₃SO₃H)
• Ethanesulfonic acid (or esylic acid, CH₃CH₂SO₃H)
• Benzenesulfonic acid (or besylic acid, C₆H₅SO₃H)
• p-Toluenesulfonic acid (or tosylic acid, CH₃C₆H₄SO₃H)
• Trifluoromethanesulfonic acid (or triflic acid, CF₃SO₃H)
• Polystyrene sulfonic acid (sulfonated polystyrene, [CH₂CH(C₆H₄)SO₃H]_n)

Carboxylic acids

A carboxylic acid has the general formula R-C(O)OH, where R is an organic radical. The carboxyl group -C(O)OH contains a carbonyl group, C=O, and a hydroxyl group, O-H.

• Acetic acid (CH₃COOH)
• Citric acid (C₆H₈O₇)
• Formic acid (HCOOH)
• Gluconic acid HOCH₂-(CHOH)₄-COOH
• Lactic acid (CH₃-CHOH-COOH)
• Oxalic acid (HOOC-COOH)
• Tartaric acid (HOOC-CHOH-CHOH-COOH)

Halogenated carboxylic acids

Halogenation at alpha position increases acid strength, so that the following acids are all stronger than acetic acid.

• Fluoroacetic acid
• Trifluoroacetic acid
• Chloroacetic acid
• Dichloroacetic acid
• Trichloroacetic acid

Vinylogous carboxylic acids

Normal carboxylic acids are the direct union of a carbonyl group and a hydroxyl group. In vinylogous carboxylic acids, a carbon-carbon double bond separates the carbonyl and hydroxyl groups.

• Ascorbic acid

Nucleic acids

• Deoxyribonucleic acid (DNA)
• Ribonucleic acid (RNA)

Lewis acids and bases

From Wikipedia, the free encyclopedia

https://en.wikipedia.org/wiki/Lewis_acids_and_bases 

 

Diagram of some Lewis bases and acids

 

Acids and bases

A Lewis acid (named for the American physical chemist Gilbert N. Lewis) is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct. A Lewis base, then, is any species that has a filled orbital containing an electron pair which is not involved in bonding but may form a dative bond with a Lewis acid to form a Lewis adduct. For example, NH₃ is a Lewis base, because it can donate its lone pair of electrons. Trimethylborane (Me₃B) is a Lewis acid as it is capable of accepting a lone pair. In a Lewis adduct, the Lewis acid and base share an electron pair furnished by the Lewis base, forming a dative bond. In the context of a specific chemical reaction between NH₃ and Me₃B, a lone pair from NH₃ will form a dative bond with the empty orbital of Me₃B to form an adduct NH₃•BMe₃. The terminology refers to the contributions of Gilbert N. Lewis.

The terms nucleophile and electrophile are more or less interchangeable with Lewis base and Lewis acid, respectively. However, these terms, especially their abstract noun forms nucleophilicity and electrophilicity, emphasize the kinetic aspect of reactivity, while the Lewis basicity and Lewis acidity emphasize the thermodynamic aspect of Lewis adduct formation.

Depicting adducts

In many cases, the interaction between the Lewis base and Lewis acid in a complex is indicated by an arrow indicating the Lewis base donating electrons toward the Lewis acid using the notation of a dative bond — for example, Me₃B←NH₃. Some sources indicate the Lewis base with a pair of dots (the explicit electrons being donated), which allows consistent representation of the transition from the base itself to the complex with the acid:

Me₃B + :NH₃ → Me₃B:NH₃

A center dot may also be used to represent a Lewis adduct, such as Me₃B·NH₃. Another example is boron trifluoride diethyl etherate, BF₃·Et₂O. In a slightly different usage, the center dot is also used to represent hydrate coordination in various crystals, as in MgSO₄·7H₂O for hydrated magnesium sulfate, irrespective of whether the water forms a dative bond with the metal.

Although there have been attempts to use computational and experimental energetic criteria to distinguish dative bonding from non-dative covalent bonds, for the most part, the distinction merely makes note of the source of the electron pair, and dative bonds, once formed, behave simply as other covalent bonds do, though they typically have considerable polar character. Moreover, in some cases (e.g., sulfoxides and amine oxides as R₂S → O and R₃N → O), the use of the dative bond arrow is just a notational convenience for avoiding the drawing of formal charges. In general, however, the donor–acceptor bond is viewed as simply somewhere along a continuum between idealized covalent bonding and ionic bonding.

Lewis acids

Major structural changes accompany binding of the Lewis base to the coordinatively unsaturated, planar Lewis acid BF₃

Lewis acids are diverse and the term is used loosely. Simplest are those that react directly with the Lewis base, such as boron trihalides and the pentahalides of phosphorus, arsenic, and antimony.

In the same vein, CH₃⁺ can be considered to be the Lewis acid in methylation reactions. However, the methyl cation never occurs as a free species in the condensed phase, and methylation reactions by reagents like CH₃I take place through the simultaneous formation of a bond from the nucleophile to the carbon and cleavage of the bond between carbon and iodine (S_N2 reaction). Textbooks disagree on this point: some asserting that alkyl halides are electrophiles but not Lewis acids, while others describe alkyl halides (e.g. CH₃Br) as a type of Lewis acid. The IUPAC states that Lewis acids and Lewis bases react to form Lewis adducts, and defines electrophile as Lewis acids.

Simple Lewis acids

Some of the most studied examples of such Lewis acids are the boron trihalides and organoboranes:

BF₃ + F⁻ → BF₄⁻

In this adduct, all four fluoride centres (or more accurately, ligands) are equivalent.

BF₃ + OMe₂ → BF₃OMe₂

Both BF₄⁻ and BF₃OMe₂ are Lewis base adducts of boron trifluoride.

Many adducts violate the octet rule, such as the triiodide anion:

I₂ + I⁻ → I₃⁻

The variability of the colors of iodine solutions reflects the variable abilities of the solvent to form adducts with the Lewis acid I₂.

Some Lewis acids binding two Lewis bases, a famous example being the formation of hexafluorosilicate:

SiF₄ + 2 F⁻ → SiF₆²⁻

Complex Lewis acids

Most compounds considered to be Lewis acids require an activation step prior to formation of the adduct with the Lewis base. Complex compounds such as Et₃Al₂Cl₃ and AlCl₃ are treated as trigonal planar Lewis acids but exist as aggregates and polymers that must be degraded by the Lewis base. A simpler case is the formation of adducts of borane. Monomeric BH₃ does not exist appreciably, so the adducts of borane are generated by degradation of diborane:

B₂H₆ + 2 H⁻ → 2 BH₄⁻

In this case, an intermediate B₂H₇⁻ can be isolated.

Many metal complexes serve as Lewis acids, but usually only after dissociating a more weakly bound Lewis base, often water.

[Mg(H₂O)₆]²⁺ + 6 NH₃ → [Mg(NH₃)₆]²⁺ + 6 H₂O

H⁺ as Lewis acid

The proton (H⁺)  is one of the strongest but is also one of the most complicated Lewis acids. It is convention to ignore the fact that a proton is heavily solvated (bound to solvent). With this simplification in mind, acid-base reactions can be viewed as the formation of adducts:

• H⁺ + NH₃ → NH₄⁺
• H⁺ + OH⁻ → H₂O

Applications of Lewis acids

A typical example of a Lewis acid in action is in the Friedel–Crafts alkylation reaction. The key step is the acceptance by AlCl₃ of a chloride ion lone-pair, forming AlCl₄⁻ and creating the strongly acidic, that is, electrophilic, carbonium ion.

RCl +AlCl₃ → R⁺ + AlCl₄⁻

Lewis bases

A Lewis base is an atomic or molecular species where the highest occupied molecular orbital (HOMO) is highly localized. Typical Lewis bases are conventional amines such as ammonia and alkyl amines. Other common Lewis bases include pyridine and its derivatives. Some of the main classes of Lewis bases are

• amines of the formula NH_3−xR_x where R = alkyl or aryl. Related to these are pyridine and its derivatives.
• phosphines of the formula PR_3−xA_x, where R = alkyl, A = aryl.
• compounds of O, S, Se and Te in oxidation state -2, including water, ethers, ketones

The most common Lewis bases are anions. The strength of Lewis basicity correlates with the pK_a of the parent acid: acids with high pK_a's give good Lewis bases. As usual, a weaker acid has a stronger conjugate base.

• Examples of Lewis bases based on the general definition of electron pair donor include:
  • simple anions, such as H⁻ and F⁻
  • other lone-pair-containing species, such as H₂O, NH₃, HO⁻, and CH₃⁻
  • complex anions, such as sulfate
  • electron-rich π-system Lewis bases, such as ethyne, ethene, and benzene

The strength of Lewis bases have been evaluated for various Lewis acids, such as I₂, SbCl₅, and BF₃.

Lewis base	Donor atom	Enthalpy of complexation (kJ/mol)
quinuclidine	N	150
Et3N	N	135
pyridine	N	128
Acetonitrile	N	60
DMA	O	112
DMSO	O	105
THF	O	90.4
Et2O	O	78.8
acetone	O	76.0
EtOAc	O	75.5
Trimethylphosphine	P	97.3
Tetrahydrothiophene	S	51.6

Applications of Lewis bases

Main article: Homogeneous catalysis

Nearly all electron pair donors that form compounds by binding transition elements can be viewed as a collections of the Lewis bases—or ligands. Thus a large application of Lewis bases is to modify the activity and selectivity of metal catalysts. Chiral Lewis bases thus confer chirality on a catalyst, enabling asymmetric catalysis, which is useful for the production of pharmaceuticals.

Many Lewis bases are "multidentate," that is they can form several bonds to the Lewis acid. These multidentate Lewis bases are called chelating agents.

Hard and soft classification

Main article: HSAB theory

Lewis acids and bases are commonly classified according to their hardness or softness. In this context hard implies small and nonpolarizable and soft indicates larger atoms that are more polarizable.

• typical hard acids: H⁺, alkali/alkaline earth metal cations, boranes, Zn²⁺
• typical soft acids: Ag⁺, Mo(0), Ni(0), Pt²⁺
• typical hard bases: ammonia and amines, water, carboxylates, fluoride and chloride
• typical soft bases: organophosphines, thioethers, carbon monoxide, iodide

For example, an amine will displace phosphine from the adduct with the acid BF₃. In the same way, bases could be classified. For example, bases donating a lone pair from an oxygen atom are harder than bases donating through a nitrogen atom. Although the classification was never quantified it proved to be very useful in predicting the strength of adduct formation, using the key concepts that hard acid—hard base and soft acid—soft base interactions are stronger than hard acid—soft base or soft acid—hard base interactions. Later investigation of the thermodynamics of the interaction suggested that hard—hard interactions are enthalpy favored, whereas soft—soft are entropy favored.

Quantifying Lewis acidity

Many methods have been devised to evaluate and predict Lewis acidity. Many are based on spectroscopic signatures such as shifts NMR signals or IR bands e.g. the Gutmann-Beckett method and the Childs method.

The ECW model is a quantitative model that describes and predicts the strength of Lewis acid base interactions, −ΔH. The model assigned E and C parameters to many Lewis acids and bases. Each acid is characterized by an E_A and a C_A. Each base is likewise characterized by its own E_B and C_B. The E and C parameters refer, respectively, to the electrostatic and covalent contributions to the strength of the bonds that the acid and base will form. The equation is

−ΔH = E_AE_B + C_AC_B + W

The W term represents a constant energy contribution for acid–base reaction such as the cleavage of a dimeric acid or base. The equation predicts reversal of acids and base strengths. The graphical presentations of the equation show that there is no single order of Lewis base strengths or Lewis acid strengths, and that single property scales are limited to a smaller range of acids or bases.

History

MO diagram depicting the formation of a dative covalent bond between two atoms

The concept originated with Gilbert N. Lewis who studied chemical bonding. In 1923, Lewis wrote An acid substance is one which can employ an electron lone pair from another molecule in completing the stable group of one of its own atoms. The Brønsted–Lowry acid–base theory was published in the same year. The two theories are distinct but complementary. A Lewis base is also a Brønsted–Lowry base, but a Lewis acid doesn't need to be a Brønsted–Lowry acid. The classification into hard and soft acids and bases (HSAB theory) followed in 1963. The strength of Lewis acid-base interactions, as measured by the standard enthalpy of formation of an adduct can be predicted by the Drago–Wayland two-parameter equation.

Reformulation of Lewis theory

Lewis had suggested in 1916 that two atoms are held together in a chemical bond by sharing a pair of electrons. When each atom contributed one electron to the bond, it was called a covalent bond. When both electrons come from one of the atoms, it was called a dative covalent bond or coordinate bond. The distinction is not very clear-cut. For example, in the formation of an ammonium ion from ammonia and hydrogen the ammonia molecule donates a pair of electrons to the proton; the identity of the electrons is lost in the ammonium ion that is formed. Nevertheless, Lewis suggested that an electron-pair donor be classified as a base and an electron-pair acceptor be classified as acid.

A more modern definition of a Lewis acid is an atomic or molecular species with a localized empty atomic or molecular orbital of low energy. This lowest-energy molecular orbital (LUMO) can accommodate a pair of electrons.

Comparison with Brønsted–Lowry theory

A Lewis base is often a Brønsted–Lowry base as it can donate a pair of electrons to H⁺; the proton is a Lewis acid as it can accept a pair of electrons. The conjugate base of a Brønsted–Lowry acid is also a Lewis base as loss of H⁺ from the acid leaves those electrons which were used for the A—H bond as a lone pair on the conjugate base. However, a Lewis base can be very difficult to protonate, yet still react with a Lewis acid. For example, carbon monoxide is a very weak Brønsted–Lowry base but it forms a strong adduct with BF₃.

In another comparison of Lewis and Brønsted–Lowry acidity by Brown and Kanner, 2,6-di-t-butylpyridine reacts to form the hydrochloride salt with HCl but does not react with BF₃. This example demonstrates that steric factors, in addition to electron configuration factors, play a role in determining the strength of the interaction between the bulky di-t-butylpyridine and tiny proton.

Allotropes of carbon

From Wikipedia, the free encyclopedia

https://en.wikipedia.org/wiki/Allotropes_of_carbon 

 

Two familiar allotropes of carbon: graphite and diamond.

 

Eight allotropes of carbon: (a) diamond, (b) graphite, (c) lonsdaleite, (d) C₆₀ buckminsterfullerene, (e) C₅₄₀ fullerite (f) C₇₀ fullerene, (g) amorphous carbon, (h) zig-zag single-walled carbon nanotube. Missing: cyclocarbon, carbon nanobuds, schwarzites, glassy carbon, and linear acetylenic carbon (carbyne)

Carbon is capable of forming many allotropes (structurally different forms of the same element) due to its valency. Well-known forms of carbon include diamond and graphite. In recent decades, many more allotropes have been discovered and researched, including ball shapes such as buckminsterfullerene and sheets such as graphene. Larger-scale structures of carbon include nanotubes, nanobuds and nanoribbons. Other unusual forms of carbon exist at very high temperatures or extreme pressures. Around 500 hypothetical 3‑periodic allotropes of carbon are known at the present time, according to the Samara Carbon Allotrope Database (SACADA).

Diamond

Main article: Diamond

Diamond is a well-known allotrope of carbon. The hardness, extremely high refractive index, and high dispersion of light make diamond useful for industrial applications and for jewellery. Diamond is the hardest known natural mineral. This makes it an excellent abrasive and makes it hold polish and luster extremely well. No known naturally occurring substance can cut or scratch diamond, except another diamond. In diamond form, carbon is one of the costliest elements.

The crystal structure of diamond is a face-centred cubic lattice having eight atoms per unit cell to form a diamond cubic structure. Each carbon atom is covalently bonded to four other carbons in a tetrahedral geometry. These tetrahedrons together form a 3-dimensional network of six-membered carbon rings in the chair conformation, allowing for zero bond angle strain. The bonding occurs through sp³ hybridized orbitals to give a C-C bond length of 154 pm. This network of unstrained covalent bonds makes diamond extremely strong. Diamond is thermodynamically less stable than graphite at pressures below 1.7 GPa.

The dominant industrial use of diamond is cutting, drilling (drill bits), grinding (diamond edged cutters), and polishing. Most uses of diamonds in these technologies do not require large diamonds, and most diamonds that are not gem-quality can find an industrial use. Diamonds are embedded in drill tips and saw blades, or ground into a powder for use in grinding and polishing applications (due to its extraordinary hardness). Specialized applications include use in laboratories as containment for high pressure experiments (see diamond anvil), high-performance bearings, and specialized windows of technical apparatuses.

The market for industrial-grade diamonds operates much differently from its gem-grade counterpart. Industrial diamonds are valued mostly for their hardness and heat conductivity, making many of the gemological characteristics of diamond, including clarity and color, mostly irrelevant. This helps explain why 80% of mined diamonds (equal to about 100 million carats or 20 tonnes annually) are unsuitable for use as gemstones and known as bort, are destined for industrial use. In addition to mined diamonds, synthetic diamonds found industrial applications almost immediately after their invention in the 1950s; another 400 million carats (80 tonnes) of synthetic diamonds are produced annually for industrial use, which is nearly four times the mass of natural diamonds mined over the same period.

With the continuing advances being made in the production of synthetic diamond, future applications are beginning to become feasible. Garnering much excitement is the possible use of diamond as a semiconductor suitable to build microchips from, or the use of diamond as a heat sink in electronics. Significant research efforts in Japan, Europe, and the United States are under way to capitalize on the potential offered by diamond's unique material properties, combined with increased quality and quantity of supply starting to become available from synthetic diamond manufacturers.

Graphite

Main article: Graphite

Graphite, named by Abraham Gottlob Werner in 1789, from the Greek γράφειν (graphein, "to draw/write", for its use in pencils) is one of the most common allotropes of carbon. Unlike diamond, graphite is an electrical conductor. Thus, it can be used in, for instance, electrical arc lamp electrodes. Likewise, under standard conditions, graphite is the most stable form of carbon. Therefore, it is used in thermochemistry as the standard state for defining the heat of formation of carbon compounds.

Graphite conducts electricity, due to delocalization of the pi bond electrons above and below the planes of the carbon atoms. These electrons are free to move, so are able to conduct electricity. However, the electricity is only conducted along the plane of the layers. In diamond, all four outer electrons of each carbon atom are 'localized' between the atoms in covalent bonding. The movement of electrons is restricted and diamond does not conduct an electric current. In graphite, each carbon atom uses only 3 of its 4 outer energy level electrons in covalently bonding to three other carbon atoms in a plane. Each carbon atom contributes one electron to a delocalized system of electrons that is also a part of the chemical bonding. The delocalized electrons are free to move throughout the plane. For this reason, graphite conducts electricity along the planes of carbon atoms, but does not conduct electricity in a direction at right angles to the plane.

Graphite powder is used as a dry lubricant. Although it might be thought that this industrially important property is due entirely to the loose interlamellar coupling between sheets in the structure, in fact in a vacuum environment (such as in technologies for use in space), graphite was found to be a very poor lubricant. This fact led to the discovery that graphite's lubricity is due to adsorbed air and water between the layers, unlike other layered dry lubricants such as molybdenum disulfide. Recent studies suggest that an effect called superlubricity can also account for this effect.

When a large number of crystallographic defects (physical) bind these planes together, graphite loses its lubrication properties and becomes pyrolytic carbon, a useful material in blood-contacting implants such as prosthetic heart valves.

Graphite is the most stable allotrope of carbon. Contrary to popular belief, high-purity graphite does not readily burn, even at elevated temperatures. For this reason, it is used in nuclear reactors and for high-temperature crucibles for melting metals. At very high temperatures and pressures (roughly 2000 °C and 5 GPa), it can be transformed into diamond.

Natural and crystalline graphites are not often used in pure form as structural materials due to their shear-planes, brittleness and inconsistent mechanical properties.

In its pure glassy (isotropic) synthetic forms, pyrolytic graphite and carbon fiber graphite are extremely strong, heat-resistant (to 3000 °C) materials, used in reentry shields for missile nosecones, solid rocket engines, high temperature reactors, brake shoes and electric motor brushes.

Intumescent or expandable graphites are used in fire seals, fitted around the perimeter of a fire door. During a fire the graphite intumesces (expands and chars) to resist fire penetration and prevent the spread of fumes. A typical start expansion temperature (SET) is between 150 and 300 °C.

Density: Graphite's specific gravity is 2.3, which makes it lighter than diamond.

Chemical activity: it is slightly more reactive than diamond. This is because the reactants are able to penetrate between the hexagonal layers of carbon atoms in graphite. It is unaffected by ordinary solvents, dilute acids, or fused alkalis. However, chromic acid oxidizes it to carbon dioxide.

Graphene

Main article: Graphene

A single layer of graphite is called graphene and has extraordinary electrical, thermal, and physical properties. It can be produced by epitaxy on an insulating or conducting substrate or by mechanical exfoliation (repeated peeling) from graphite. Its applications may include replacing silicon in high-performance electronic devices. With two layers stacked, bilayer graphene results with different properties.

Lonsdaleite (hexagonal diamond)

Lonsdaleite is an allotrope sometimes called "hexagonal diamond", formed from graphite present in meteorites upon their impact on the earth. The great heat and pressure of the impact transforms the graphite into a denser form similar to diamond, but retaining graphite's hexagonal crystal lattice. "Hexagonal diamond" has also been synthesized in the laboratory, by compressing and heating graphite either in a static press or using explosives. It can also be produced by the thermal decomposition of a polymer, poly(hydridocarbyne), at atmospheric pressure, under inert gas atmosphere (e.g. argon, nitrogen), starting at temperature 110 °C (230 °F).

Graphenylene

Graphenylene is a single layer carbon material with biphenylene-like subunits as basis in its hexagonal lattice structure. It is also known as biphenylene-carbon.

Carbophene

Carbophene is a 2 dimensional covalent organic framework. 4-6 carbophene has been synthesized from 1-3-5 trihydroxybenzene. It consists of 4-carbon and 6-carbon rings in 1:1 ratio. The angles between the three σ-bonds of the orbitals are approximately 120°, 90°, and 150°.

AA'-graphite

AA'-graphite is an allotrope of carbon similar to graphite, but where the layers are positioned differently to each other as compared to the order in graphite.

Diamane

Diamane is a 2D form of diamond. It can be made via high pressures, but without that pressure, the material reverts to graphene. Another technique is to add hydrogen atoms but those bonds are weak. Using fluorine (xenon-difluoride) instead brings the layers closer together, strengthening the bonds. This is called f-diamane.

Amorphous carbon

Main article: Amorphous carbon

Amorphous carbon is the name used for carbon that does not have any crystalline structure. As with all glassy materials, some short-range order can be observed, but there is no long-range pattern of atomic positions. While entirely amorphous carbon can be produced, most amorphous carbon actually contains microscopic crystals of graphite-like, or even diamond-like carbon.

Coal and soot or carbon black are informally called amorphous carbon. However, they are products of pyrolysis (the process of decomposing a substance by the action of heat), which does not produce true amorphous carbon under normal conditions.

Nanocarbons

Buckminsterfullerenes

Main article: Fullerene

The buckminsterfullerenes, or usually just fullerenes or buckyballs for short, were discovered in 1985 by a team of scientists from Rice University and the University of Sussex, three of whom were awarded the 1996 Nobel Prize in Chemistry. They are named for the resemblance to the geodesic structures devised by Richard Buckminster "Bucky" Fuller. Fullerenes are positively curved molecules of varying sizes composed entirely of carbon, which take the form of a hollow sphere, ellipsoid, or tube.

As of the early twenty-first century, the chemical and physical properties of fullerenes are still under heavy study, in both pure and applied research labs. In April 2003, fullerenes were under study for potential medicinal use — binding specific antibiotics to the structure to target resistant bacteria and even target certain cancer cells such as melanoma.

Carbon nanotubes

Main article: Carbon nanotube

Carbon nanotubes, also called buckytubes, are cylindrical carbon molecules with novel properties that make them potentially useful in a wide variety of applications (e.g., nano-electronics, optics, materials applications, etc.). They exhibit extraordinary strength, unique electrical properties, and are efficient conductors of heat. Non-carbon nanotubes have also been synthesized. Carbon nanotubes are a members of the fullerene structural family, which also includes buckyballs. Whereas buckyballs are spherical in shape, a nanotube is cylindrical, with at least one end typically capped with a hemisphere of the buckyball structure. Their name is derived from their size, since the diameter of a nanotube is on the order of a few nanometers (approximately 50,000 times smaller than the width of a human hair), while they can be up to several centimeters in length. There are two main types of nanotubes: single-walled nanotubes (SWNTs) and multi-walled nanotubes (MWNTs).

Carbon nanobuds

Computer models of stable nanobud structures

 

Main article: Carbon nanobud

Carbon nanobuds are a newly discovered allotrope of carbon in which fullerene like "buds" are covalently attached to the outer sidewalls of the carbon nanotubes. This hybrid material has useful properties of both fullerenes and carbon nanotubes. For instance, they have been found to be exceptionally good field emitters.

Schwarzites

Schwarzites are negatively curved carbon surfaces originally proposed by decorating triply periodic minimal surfaces with carbon atoms. The geometric topology of the structure is determined by the presence of ring defects, such as heptagons and octagons, to graphene's hexagonal lattice. (Negative curvature bends surfaces outwards like a saddle rather than bending inwards like a sphere.)

Recent work has proposed zeolite-templated carbons (ZTCs) may be schwarzites. The name, ZTC, derives from their origin inside the pores of zeolites, crystalline silicon dioxide minerals. A vapor of carbon-containing molecules is injected into the zeolite, where the carbon gathers on the pores' walls, creating the negative curve. Dissolving the zeolite leaves the carbon. A team generated structures by decorating the pores of a zeolite with carbon through a Monte Carlo method. Some of the resulting models resemble schwarzite-like structures.

Glassy carbon

A large sample of glassy carbon.

 

Main article: Glassy carbon

Glassy carbon or vitreous carbon is a class of non-graphitizing carbon widely used as an electrode material in electrochemistry, as well as for high-temperature crucibles and as a component of some prosthetic devices.

It was first produced by Bernard Redfern in the mid-1950s at the laboratories of The Carborundum Company, Manchester, UK. He had set out to develop a polymer matrix to mirror a diamond structure and discovered a resole (phenolic) resin that would, with special preparation, set without a catalyst. Using this resin the first glassy carbon was produced.

The preparation of glassy carbon involves subjecting the organic precursors to a series of heat treatments at temperatures up to 3000 °C. Unlike many non-graphitizing carbons, they are impermeable to gases and are chemically extremely inert, especially those prepared at very high temperatures. It has been demonstrated that the rates of oxidation of certain glassy carbons in oxygen, carbon dioxide or water vapor are lower than those of any other carbon. They are also highly resistant to attack by acids. Thus, while normal graphite is reduced to a powder by a mixture of concentrated sulfuric and nitric acids at room temperature, glassy carbon is unaffected by such treatment, even after several months.

Atomic and diatomic carbon

Main articles: Atomic carbon and diatomic carbon

Under certain conditions, carbon can be found in its atomic form. It can be formed by vaporizing graphite, by passing large electric currents to form a carbon arc under very low pressures. It is extremely reactive, but it is an intermediate product used in the creation of carbenes.

Diatomic carbon can also be found under certain conditions. It is often detected via spectroscopy in extraterrestrial bodies, including comets and certain stars.

Carbon nanofoam

Main article: Carbon nanofoam

Carbon nanofoam is the fifth known allotrope of carbon, discovered in 1997 by Andrei V. Rode and co-workers at the Australian National University in Canberra. It consists of a low-density cluster-assembly of carbon atoms strung together in a loose three-dimensional web.

Each cluster is about 6 nanometers wide and consists of about 4000 carbon atoms linked in graphite-like sheets that are given negative curvature by the inclusion of heptagons among the regular hexagonal pattern. This is the opposite of what happens in the case of buckminsterfullerenes, in which carbon sheets are given positive curvature by the inclusion of pentagons.

The large-scale structure of carbon nanofoam is similar to that of an aerogel, but with 1% of the density of previously produced carbon aerogels – only a few times the density of air at sea level. Unlike carbon aerogels, carbon nanofoam is a poor electrical conductor.

Carbide-derived carbon

Main article: Carbide-derived carbon

Carbide-derived carbon (CDC) is a family of carbon materials with different surface geometries and carbon ordering that are produced via selective removal of metals from metal carbide precursors, such as TiC, SiC, Ti₃AlC₂, Mo₂C, etc. This synthesis is accomplished using chlorine treatment, hydrothermal synthesis, or high-temperature selective metal desorption under vacuum. Depending on the synthesis method, carbide precursor, and reaction parameters, multiple carbon allotropes can be achieved, including endohedral particles composed of predominantly amorphous carbon, carbon nanotubes, epitaxial graphene, nanocrystalline diamond, onion-like carbon, and graphitic ribbons, barrels, and horns. These structures exhibit high porosity and specific surface areas, with highly tunable pore diameters, making them promising materials for supercapacitor-based energy storage, water filtration and capacitive desalinization, catalyst support, and cytokine removal.

Linear acetylenic carbon

Main article: Linear acetylenic carbon

A one-dimensional carbon polymer with the structure —(C≡C)_n—.

Cyclocarbons

Main article: Cyclocarbon

Cyclo[18]carbon (C₁₈) was synthesised in 2019.

Other possible allotropes

Many other allotropes have been hypothesized but have yet to be synthesized.

• 

• Crystal structure of the proposed C₈ cubic form of carbon
  bcc-carbon: At ultrahigh pressures of above 1000 GPa, diamond is predicted to transform into a body-centred cubic structure. This phase has importance in astrophysics and deep interiors of planets like Uranus and Neptune. Various structures have been proposed. Superdense and superhard material resembling this phase was synthesized and published in 1979 and reported to have the Im3 space group with eight atoms per primitive unit cell (16 atoms per conventional unit cell). Claims were made that the so-called C₈ structure had been synthesized, having eight-carbon cubes similar to cubane in the Im3m space group, with eight atoms per primitive unit cell, or 16 atoms per conventional unit cell (also called supercubane, see illustration to the right). But a paper in 1988 claimed that a better theory was that the structure was the same as that of an allotrope of silicon called Si-III or γ-silicon, the so-called BC8 structure with space group Ia3 and 8 atoms per primitive unit cell (16 atoms per conventional unit cell). In 2008 it was reported that the cubane-like structure had been identified. A paper in 2012 considered four proposed structures, the supercubane structure, the BC8 structure, a structure with clusters of four carbon atoms in tetrahedra in space group I43m having four atoms per primitive unit cell (eight per conventional unit cell), and a structure the authors called "carbon sodalite". They found in favor of this carbon sodalite structure, with a calculated density of 2.927 g/cm³, shown in the upper left of the illustration under the abstract. This structure has just six atoms per primitive unit cell (twelve per conventional unit cell). The carbon atoms are in the same locations as the silicon and aluminum atoms of the mineral sodalite. The space group, I43m, is the same as the fully expanded form of sodalite would have if sodalite had just silicon or just aluminum.

• bct-carbon: Body-centered tetragonal carbon was proposed by theorists in 2010.
• Chaoite is a mineral believed to have been formed in meteorite impacts. It has been described as slightly harder than graphite with a reflection color of grey to white. However, the existence of carbyne phases is disputed – see the article on chaoite for details.
• D-carbon: D-carbon was proposed by theorists in 2018. D-carbon is an orthorhombic sp³ carbon allotrope (6 atoms per cell). Total-energy calculations demonstrate that D-carbon is energetically more favorable than the previously proposed T₆ structure (with 6 atoms per cell) as well as many others.
• Haeckelites: Ordered arrangements of pentagons, hexagons, and heptagons which can either be flat or tubular.

The K₄ crystal

• The Laves graph or K₄ crystal is a theoretically predicted three-dimensional crystalline metastable carbon structure in which each carbon atom is bonded to three others, at 120° angles (like graphite), but where the bond planes of adjacent layers lie at an angle of 70.5°, rather than coinciding.
• M-carbon: Monoclinic C-centered carbon is thought to have been first created in 1963 by compressing graphite at room temperature. Its structure was theorized in 2006, then in 2009 it was related to those experimental observations. Many structural candidates, including bct-carbon, were proposed to be equally compatible with experimental data available at the time, until in 2012 it was shown theoretically that this structure is kinetically the most likely to form from graphite. High-resolution data appeared shortly after, demonstrating that among all structure candidates only M-carbon is compatible with experiment.
• Metallic carbon: Theoretical studies have shown that there are regions in the phase diagram, at extremely high pressures, where carbon has metallic character. Laser shock experiments and theory indicate that above 600 GPa liquid carbon is metallic.
• Novamene: A combination of both hexagonal diamond and sp² hexagons as in graphene.
• Phagraphene: Graphene-like allotrope with distorted Dirac cones.
• Prismane C₈ is a theoretically predicted metastable carbon allotrope comprising an atomic cluster of eight carbon atoms, with the shape of an elongated triangular bipyramid—a six-atom triangular prism with two more atoms above and below its bases.
• Protomene: A hexagonal crystal structure with a fully relaxed primitive cell involving 48 atoms. Out of these, 12 atoms have the potential to switch hybridization between sp² and sp³, forming dimers.
• Q-carbon: Ferromagnetic carbon was discovered in 2015.
• T-carbon: Every carbon atom in diamond is replaced with a carbon tetrahedron (hence 'T-carbon'). This was proposed by theorists in 1985.
• There is evidence that white dwarf stars have a core of crystallized carbon and oxygen nuclei. The largest of these found in the universe so far, BPM 37093, is located 50 light-years (4.7×10¹⁴ km) away in the constellation Centaurus. A news release from the Harvard-Smithsonian Center for Astrophysics described the 2,500-mile (4,000 km)-wide stellar core as a diamond, and it was named as Lucy, after the Beatles' song "Lucy in the Sky With Diamonds"; however, it is more likely an exotic form of carbon. Penta-graphene is a predicted carbon allotrope that utilizes the Cairo pentagonal tiling.
• U carbon is predicted to consist of corrugated layers tiled with six- or 12-atom rings, linked by covalent bonds. Notably, it can be harder than steel, as conductive as stainless steel, highly reflective and ferromagnetic, behaving as a permanent magnet at temperatures up to 125 °C.

• Zayedene: A combination of linear sp carbon chains and sp3 bulk carbon. The structure of these crystalline carbon allotropes consists of sp chains inserted in cylindrical cavities periodically arranged in hexagonal diamond (lonsdaleite).

Variability of carbon

Diamond and graphite are two allotropes of carbon: pure forms of the same element that differ in structure.

The system of carbon allotropes spans an astounding range of extremes, considering that they are all merely structural formations of the same element.

Between diamond and graphite:

• Diamond crystallizes in the cubic system but graphite crystallizes in the hexagonal system.
• Diamond is clear and transparent, but graphite is black and opaque.
• Diamond is the hardest mineral known (10 on the Mohs scale), but graphite is one of the softest (1–2 on Mohs scale).
• Diamond is the ultimate abrasive, but graphite is soft and is a very good lubricant.
• Diamond is an excellent electrical insulator, but graphite is an excellent conductor.
• Diamond is an excellent thermal conductor, but some forms of graphite are used for thermal insulation (for example heat shields and firebreaks).
• At standard temperature and pressure, graphite is the thermodynamically stable form. Thus diamonds do not exist forever. The conversion from diamond to graphite, however, has a very high activation energy and is therefore extremely slow.

Despite the hardness of diamonds, the chemical bonds that hold the carbon atoms in diamonds together are actually weaker than those that hold together graphite. The difference is that in diamond, the bonds form an inflexible three-dimensional lattice. In graphite, the atoms are tightly bonded into sheets, but the sheets can slide easily over each other, making graphite soft.