Oxidation state

The oxidation state, often called the oxidation number, is an indicator of the degree of oxidation (loss of electrons) of an atom in a chemical compound. Conceptually, the oxidation state, which may be positive, negative or zero, is the hypothetical charge that an atom would have if all bonds to atoms of different elements were 100% ionic, with no covalent component. This is never exactly true for real bonds.

The term "oxidation" was first used by Lavoisier to mean reaction of a substance with oxygen. Much later, it was realized that the substance, upon being oxidized, loses electrons, and the use of the term "oxidation" was extended to include other reactions in which electrons are lost.

Oxidation states are typically represented by integers. In some cases, the average oxidation state of an element is a fraction, such as 8⁄3 for iron in magnetite (Fe
3O
4). The highest known oxidation state is reported to be +9 in the iridium tetroxide cation (IrO+
4),[1] while the lowest known oxidation state is −5 for boron, gallium, indium, and thallium in various intermetallic compounds.[2] The possibility of +10 oxidation states in platinum group elements, especially platinum(X), has been discussed by Kiselev and Tretiyakov.[3]

The increase in oxidation state of an atom, through a chemical reaction, is known as an oxidation; a decrease in oxidation state is known as a reduction. Such reactions involve the formal transfer of electrons: a net gain in electrons being a reduction, and a net loss of electrons being an oxidation. For pure elements, the oxidation state is zero.

There are various methods for determining oxidation states.

In inorganic nomenclature, the oxidation state is determined and expressed as an oxidation number, and is represented by a Roman numeral placed after the element name.

In coordination chemistry, "oxidation number" is defined differently from "oxidation state".

IUPAC definitions of oxidation state and oxidation number

Oxidation state

A IUPAC technical report Toward a comprehensive definition of oxidation state has been published.[4] The current Gold Book definition of oxidation state listed by IUPAC is as follows:[5]

Oxidation state is defined as the charge an atom might be imagined to have when electrons are counted according to an agreed-upon set of rules:
  1. the oxidation state of a free element (uncombined element) is zero
  2. for a simple (monatomic) ion, the oxidation state is equal to the net charge on the ion
  3. hydrogen has an oxidation state of +1 and oxygen has an oxidation state of −2 when they are present in most compounds. Exceptions to this are that hydrogen has an oxidation state of −1 in hydrides of active metals, e.g. LiH, and oxygen has an oxidation state of −1 in peroxides, e.g. H
    2    O
    2    .
  4. the algebraic sum of oxidation states of all atoms in a neutral molecule must be zero, while in ions the algebraic sum of the oxidation states of the constituent atoms must be equal to the charge on the ion.

Determining the oxidation state or number

There are two different methods for determining the oxidation state of elements in chemical compounds. First (and widely taught) a method based on the rules in the IUPAC definition (see above). Second, a method based on the relative electronegativity of the elements in the compound, where the more electronegative element is assumed to take the negative charge.

Simple examples using IUPAC definition

  1. An application of this rule is that the sum of the oxidation states of all atoms in a neutral molecule must be zero. Consider a neutral molecule of carbon dioxide, CO
    2    . Oxygen is assumed to have its usual oxidation state of −2, and so the sum of the oxidation states of all the atoms can be expressed as x + 2(−2) = 0, or x − 4 = 0, where x is the unknown oxidation state of carbon. Thus, it can be seen that the oxidation state of carbon in the molecule is +4.
  2. In polyatomic ions, the sum of the oxidation states of the constituent atoms must be equal to the charge on the ion. As an example, consider the sulfate anion, which has the formula SO2−
    4    . As indicated by the formula, the total charge of this ion is −2. Because all four oxygen atoms are assumed to have their usual oxidation state of −2, and the sum of the oxidation states of all the atoms is equal to the charge of the ion, the sum of the oxidation states can be represented as y + 4(−2) = −2, or y − 8 = −2, where y is the unknown oxidation state of sulfur. Thus, it can be computed that y = +6.

These facts, combined with some elements almost always having certain oxidation states (due to their very high electropositivity or electronegativity), allows one to compute the oxidation states for the remaining atoms (such as transition metals) in simple compounds.

Example for a complex salt: In Cr(OH)
3, oxygen has an oxidation state of −2 (no fluorine or O−O bonds present), and hydrogen has a state of +1 (bonded to oxygen). So, each of the three hydroxide groups has an overall oxidation state of −2 + 1 = −1. As the compound is neutral, chromium has an oxidation state of +3.

Using electronegativity

The use of electronegativity in this way was introduced by Linus Pauling in 1947.[6] This method of determining oxidation state is found in some recent text books.[7] This method allows the oxidation state of all atoms in a molecule to be determined whereas the IUPAC 1990/2005 definition does not.[8] In the 1970 rules,[9] IUPAC recommended that oxidation state was used in nomenclature and elsewhere in inorganic chemistry as the "charge that would be present on an atom if the electrons were assigned to the more electronegative atom", but with a convention that hydrogen is considered to be positive in combination with nonmetals and a bond between like atoms makes no contribution to the oxidation number.

In practice the IUPAC 1990/2005 definition is usually extended by adding additional rules based on electronegativity.

Ionic compounds

If an ionic compound has two ions with a common element, such as ammonium nitrate, NH
4NO
3, it is usual to consider the oxidation states for each ion separately. The overall empirical formula of ammonium nitrate is N
2H
4O
3, so that 2x + 4(1) + 3(−2) = 0, and the average nitrogen oxidation state x = +1. However it is much more useful to consider separately the ions NH+
4 and NO−
3 with nitrogen oxidation states of −3 and +5 respectively.[10]

Calculation of oxidation states with a Lewis structure

This method can be used for molecules when one has a Lewis structure.

It should be remembered that the oxidation state of an atom does not represent the "real" charge on that atom. This is particularly true of high oxidation states, where the ionization energy required to produce a multiply positive ion are far greater than the energies available in chemical reactions. The assignment of electrons between atoms in calculating an oxidation state is purely a formalism, but is a useful one for the understanding of many chemical reactions.

For more about issues with calculating atomic charges, see partial charge.

The Lewis structure

When a Lewis structure of a molecule is available, the oxidation states may be assigned by computing the difference between the number of valence electrons that a neutral atom of that element would have and the number of electrons that "belong" to it in the Lewis structure. For purposes of computing oxidation states, electrons in a bond between atoms of different elements belong to the more electronegative atom; electrons in a bond between atoms of the same element are split equally, and electrons in a lone pair belong only to the atom with the lone pair.[11]

For example, consider acetic acid:

The methyl group carbon atom has six valence electrons from its bonds to the hydrogen atoms because carbon is more electronegative than hydrogen. Also, one electron is gained from its bond with the other carbon atom because the electron pair in the C−C bond is split equally. It therefore has a total of seven electrons, whereas a neutral carbon atom would have four valence electrons because carbon is in group 14 of the periodic table. The difference, 4 − 7 = −3, is the oxidation state of that carbon atom. That is, if it is assumed that all the bonds were 100% ionic (which in fact they are not), the carbon would be described as C3−
.

Following the same rules, the carboxylic acid carbon atom gets the other one valence electron from the C−C bond. All of its other valence electrons are not counted here because they are involved in bonding to oxygen atoms, which are more electronegative than carbon. For a carbon with one electron, the oxidation state is +3, again calculated against its neutral four-electron count. The oxygen atoms each have an oxidation state of −2; they get 8 electrons each (4 from the lone pairs and 4 from the bonds), while a neutral oxygen atom would have 6. The hydrogen atoms each have oxidation state +1, because they surrender their electron to the more electronegative atoms to which they are bonded.

In structural diagrams for organic chemistry, oxidation states are represented by Roman numerals to distinguish them from formal charges (calculated with all bonds covalent).

Inequivalent atoms of an element

Structure of the thiosulfate anion

An example of a molecule with inequivalent atoms of the same element is the thiosulfate ion (S
2O2−
3), for which the algebraic sum rule yields the average value +2 for sulfur, where the two ionizing electrons are assigned to the terminal sulfur atom. However, the use of a Lewis structure and electron counting shows that the two sulfur atoms are different. The central sulfur is assigned only one valence electron from the S−S bond and no valence electrons from the S−O bonds, compared to six valence electrons for a free sulfur atom, so the oxidation state of the central sulfur is +5. The terminal sulfur atom is assigned the other electron from the S−S bond plus three lone pairs for a total of seven valence electrons, so its oxidation state is −1.

Redox reactions

Oxidation states can be useful for balancing chemical equations for oxidation–reduction (or redox) reactions, because the changes in the oxidized atoms have to be balanced by the changes in the reduced atoms. For example, in the reaction of acetaldehyde with the Tollens' reagent to acetic acid (shown below), the carbonyl carbon atom changes its oxidation state from +1 to +3 (oxidation). This oxidation is balanced by reducing two equivalents of silver from Ag+ to Ag0.

Elements with multiple oxidation states

Most elements have more than one possible oxidation state. For example, carbon has nine integer oxidation states:

Integer oxidation states of carbon
Oxidation state Example compound
−4 CH
4
−3 C
2H
6
−2 CH
3Cl
−1 C
2H
2
0 CH
2Cl
2
+1 CHCl
2CHCl
2
+2 CHCl
3
+3 C
2Cl
6
+4 CCl
4

Fractional oxidation states

Fractional oxidation states are often used to represent the average oxidation states of several atoms of the same element in a structure. For example, the formula of magnetite is Fe
3O
4, implying an oxidation state for iron of +8⁄3.[10] However this average value may not be representative if the atoms are not equivalent. In Fe
3O
4, two-thirds of the iron ions are Fe3+
 and one-third Fe2+
, and the formula may be better represented as FeO·Fe
2O
3.[10]

Likewise, propane, C
3H
8, has been described as having a carbon oxidation state of −8⁄3.[12] Again this is an average value since the structure of the molecule is H
3C−CH
2−CH
3, with the first and third carbons each having an oxidation state of −3 and the central one −2.

An example with true fractional oxidation states for equivalent atoms is potassium superoxide, KO
2. The diatomic superoxide ion has an overall charge of −1, so each of its two oxygen atoms is assigned an oxidation state of −1⁄2, This ion can be described as a resonance hybrid of two Lewis structures, where each oxygen has oxidation state 0 in one structure and −1 in the other.

For the cyclopentadienyl ion C
5H−
5, the oxidation state of C is (−1) + (−1⁄5) = −6⁄5. The −1 occurs because each C is bonded to one hydrogen (a less electronegative element), and the −1⁄5 because the total ionic charge of −1 is divided among five equivalent C.

Examples of fractional oxidation states for carbon
Oxidation state Example species
−6⁄5 C
5H−
5
−6⁄7 C
7H+
7
−5⁄4 C
8H2−
8

Oxidation state and formal charge

The oxidation state of an atom is often different from the formal charge often included in Lewis structures (when it is non-zero). The oxidation state is calculated by assuming that each chemical bond (except between identical atoms) is ionic so that both electrons are assigned to the more electronegative bonded atom. In contrast, the formal charge is calculated by assuming that each bonds is covalent so that one electron is assigned to each bonded atom. For example, in ammonium ion (NH+
4) the oxidation state of nitrogen is −3, as all eight valence electrons are assigned to the nitrogen atom that is more electronegative than hydrogen. However, the formal charge is +1, calculated by assigning only four valence electrons (one per bond) to nitrogen. For comparison, the nitrogen in ammonia (NH
3) has oxidation state −3 also but a formal charge of zero. On protonation of ammonia to form ammonium, the formal charge on nitrogen changes, but its oxidation state does not.

Oxidation number in naming of inorganic compounds

In the nomenclature of inorganic compounds, the oxidation number is represented by a Roman numeral. The oxidation number is equal to the oxidation state using the rules, although they acknowledge other methods can be used. Oxidation numbers must be positive or negative integers, fractional oxidation numbers should not be used, and in the event of any uncertainty alternative naming conventions should be used.

Use in nomenclature

In older literature the term is referred to as Stock number. However, the use of this term is no longer recommended by IUPAC.[13] The oxidation state in compound naming is placed either as a right superscript to the element symbol in chemical formula, for example FeIII, or in parentheses after the name of the element, iron(III) in chemical names. For example, Fe
2(SO
4)
3 is named iron(III) sulfate and its formula can be shown as FeIII
2(SO
4)
3. This is because a sulfate ion has a charge of −2, so each iron atom takes a charge of +3. Note that fractional oxidation numbers should not be used in naming.[14] Magnetite, Fe
3O
4, is represented as iron(II,III) oxide, showing the mixture of oxidation states of the nonequivalent iron atoms.

Oxidation number in coordination compounds

While oxidation state and oxidation number are often used interchangeably, oxidation number is used in coordination chemistry with a slightly different meaning. In coordination chemistry, the rules used for counting electrons are different. Every electron in a metal–ligand bond belongs to the ligand, regardless of electronegativity, so that the oxidation number is the charge that would remain if all ligands were removed together with the electron pairs shared with the central atom.[15]

The current IUPAC definition of the oxidation number in a coordination compound is as follows:[16]

Of a central atom in a coordination entity, the charge it would bear if all the ligands were removed along with the electron pairs that were shared with the central atom. It is represented by a Roman numeral.

For most coordination complexes, the metal atom is the less electronegative end of each metal–ligand bond, so that this rule gives the same result as the electronegativity-based rule[8] There are exceptions, however, such as Wilkinson's catalyst, RhCl(PPh
3)
3 (Ph = phenyl), in which the rhodium atom is more electronegative than phosphorus. Nevertheless, the oxidation number of rhodium in this molecule is considered to be +1 and the molecule's systematic name is chlorotris(triphenylphosphine)rhodium(I), as the electrons of each Rh−P bond are assigned to the P atom of the ligand. The electronegativity rule would assign them instead to the Rh with an oxidation state of −5.

Spectroscopic oxidation states versus oxidation numbers

Although oxidation numbers can be helpful for classifying compounds, they are unmeasurable and their physical meaning can be ambiguous. Oxidation numbers require particular caution for molecules where the bonding is covalent, since the oxidation numbers require the heterolytic removal of ligands, which in essence denies covalency. Spectroscopic oxidation states, as defined by Jorgenson and reiterated by Wieghardt, are measurables that are benchmarked using spectroscopic and crystallographic data.[17]

Oxidation state can also have effect on spectroscopic studies of compounds. In infrared spectroscopy of metal carbonyls this effect is illustrated by using spectroscopic studies on metals from oxidation states of −2 to +2.

Unusual oxidation states

Unusual oxidation states of metals are important in biochemical processes, the notable ones being Fe(IV) and Fe(V) in cytochrome P450-containing systems.

History of the oxidation number concept

First study

Oxidation itself was first studied by Antoine Lavoisier, who believed that what we now call oxidation was always the result of reactions with oxygen,[18] thus the name. Although Lavoisier's idea has been shown to be incorrect, the name he proposed is still used, albeit more generally.

Oxidation states were one of the intellectual stepping stones that Mendeleev used to derive the periodic table.

Nomenclature

When it was realized that some metals form two different binary compounds with the same nonmetal, the two compounds were often distinguished by using the ending -ic for the higher metal oxidation state and the ending -ous for the lower. For example FeCl3 is ferric chloride and FeCl2 is ferrous chloride. This system is not very satisfactory (although sometimes still used) because different metals have different oxidation states which have to be learned: ferric and ferrous are +3 and +2 respectively, but cupric and cuprous are +2 and +1, and stannic and stannous are +4 and +2. Also there was no allowance for metals with more than two oxidation states, such as vanadium with oxidation states +2, +3, +4 and +5.[19]

This system has been largely replaced by Stock nomenclature (named for Alfred Stock who suggested it in 1919). Under the Stock system FeCl
2 is called iron(II) chloride rather than ferrous chloride.

Current concept

The current concept of "oxidation state" was introduced by W. M. Latimer in 1938.[20] In 1940 IUPAC recommended that the term Stock number should be replaced by the term oxidation number. In 1947 Linus Pauling proposed that the oxidation number could be determined using the electronegativity of the atoms to determine the "ions" in the formal determination of oxidation number.[6] In 1970[9] IUPAC defined oxidation number in terms of electronegativity. In 1990 IUPAC changed course and adopted a rule based determination for the "central atom" rather than using electronegativity. This is the definition in the current Gold Book for "oxidation state". They also introduced the definition of oxidation number, shown in the current Gold Book, that appears to make oxidation number specific to coordination chemistry. This may not have been their intention, as in 2005 they issued new recommendations for inorganic nomenclature that define oxidation number in the same terms as the 1990 definition of oxidation state, and that oxidation number is, as in the earlier recommendations, used in the naming of inorganic compounds.

Oxidation number versus oxidation state

In general, in the wider field of chemistry the IUPAC definitions have not been adhered to and both terms are used interchangeably, as they were when Latimer introduced the concept in 1938.[20] For example, two well-known textbooks[21][22] use the term oxidation state and represent it in Roman numerals in chemical formulae. The point has been made that, if there is any semantic difference between the terms, then oxidation number refers to the specific numerical value assigned to the entity known as oxidation state, much as IUPAC use the term charge number to refer to the numerical value assigned to the entity known as ionic charge.[23] The IUPAC Gold Book takes the definitions from 1990 IUPAC papers[24][25] rather than the more recent current IUPAC 2005 recommendations. An IUPAC project, "Towards a comprehensive definition of oxidation state", (project 2008-040-1-200) started in 2009. The technical report has been published in Pure and Applied Chemistry.[4] The project was undertaken because the current definition in the IUPAC Gold Book was seen to be "narrow and circular", and "inapplicable to clusters, Zintl phases and some organometallic complexes".[26]

See also

References

  1. ↑ Wang, Guanjun; Zhou, Mingfei; Goettel, James T.; Schrobilgen, Gary G.; Su, Jing; Li, Jun; Schlöder, Tobias; Riedel, Sebastian (23 October 2014). "Identification of an iridium-containing compound with a formal oxidation state of IX". Nature 514: 475–477. doi:10.1038/nature13795.
  2. ↑ See annotated cites for these elements at List of oxidation states of the elements.
  3. ↑ Kiselev, Yurii M. and Tretiyakov, Yurii D. (1999), Russian Chemical Reviews, 68, 365−379 "The problem of oxidation state stabilisation and some regularities of a Periodic system of the elements"
  4. 1 2 Karen, Pavel; McArdle, Patrick; Takats, Josef (2014). "Toward a comprehensive definition of oxidation state (IUPAC Technical Report)". Pure and Applied Chemistry 86 (6). doi:10.1515/pac-2013-0505.
  5. ↑ IUPAC Gold Book definition: oxidation state
  6. 1 2 General Chemistry: An Introduction to Descriptive Chemistry and Modern Chemical Theory, Linus Pauling, W.H Freeman, 1947
  7. ↑ Basic Concepts of Chemistry, 8th Edition, Leo J. Malone, Theodore Dolter, John Wiley & Sons, 2008, ISBN 978-0471741541
  8. 1 2 Loock, Hans-Peter (2011). "Expanded Definition of the Oxidation State". Journal of Chemical Education 88 (3): 282–283. doi:10.1021/ed1005213. ISSN 0021-9584.
  9. 1 2 Nomenclature of Inorganic chemistry, 2d Edition, Definitive rules 1970, Butterworths
  10. 1 2 3 Petrucci R.H., Harwood W.S. and Herring F.G. General Chemistry (8th ed., Prentice-Hall 2002) pp. 81–82
  11. ↑ Spencer J.N., Bodner G.M. and Rickard L.H. Chemistry: Structure and Dynamics (5th ed., Wiley 2010), p.543. This reference uses 1-propanol as an example.
  12. ↑ Whitten K.W., Galley K.D. and Davis R.E. General Chemistry (4th ed., Saunders 1992) p.147
  13. ↑ IUPAC Gold Book definition: Stock number
  14. ↑ Nomenclature of Inorganic Chemistry IUPAC Recommendations 2005 ed. N. G. Connelly et al. RSC Publishing http://www.old.iupac.org/publications/books/rbook/Red_Book_2005.html.
  15. ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "oxidation number".
  16. ↑ IUPAC Gold Book definition: oxidation number
  17. ↑ Bill, E.; Bothe, E.; Chaudhuri, P.; Chlopek, K.; Herebian, D.; Kokatam, S.; Ray, K.; Weyhermueller, T.; Neese, F.; Wieghardt, K. (2005). "Molecular and electronic structure of four- and five-coordinate cobalt complexes containing two o-phenylenediamine- or two o-aminophenol-type ligands at various oxidation levels functional, and correlated ab initio study". Chemistry – A European Journal 11 (1): 204–224. doi:10.1002/chem.200400850. PMID 15549762.
  18. ↑ The Origin of the Oxidation-State Concept William B. Jensen J. Chem. Educ. 2007, 84, 1418
  19. ↑ Petrucci R.H., Harwood W.S. and Herring F.G. General Chemistry (8th ed., Prentice-Hall 2002), p.84 ISBN 0-13-014329-4
  20. 1 2 Jensen, William B. (2007). "The Origin of the Oxidation-State Concept". Journal of Chemical Education 84 (9): 1418. doi:10.1021/ed084p1418. ISSN 0021-9584.
  21. ↑ Cotton, F. Albert; Wilkinson, Geoffrey; Murillo, Carlos A.; Bochmann, Manfred (1999), Advanced Inorganic Chemistry (6th ed.), New York: Wiley-Interscience, ISBN 0-471-19957-5
  22. ↑ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0-08-037941-9.
  23. ↑ Jensen, William B. (2011). "Oxidation States versus Oxidation Numbers". Journal of Chemical Education 88 (12): 1599–1600. doi:10.1021/ed2001347. ISSN 0021-9584.
  24. ↑ Red Book: IUPAC Nomenclature of Inorganic Chemistry. Third Edition, Blackwell Scientific Publications, Oxford, 1990.
  25. ↑ Calvert, J. G. (1990). "Glossary of atmospheric chemistry terms (Recommendations 1990)". Pure and Applied Chemistry 62 (11): 2167–2219. doi:10.1351/pac199062112167. ISSN 0033-4545.
  26. ↑ "Project Details: Towards a comprehensive definition of oxidation state". IUPAC. March 10, 2014. Retrieved May 1, 2014.
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