Hydron (chemistry)

In chemistry, a hydron is the general name for a cationic form of atomic hydrogen, represented with the symbol H+
. However, virtually all chemists will call this species the "proton", which strictly speaking refers to the cation of protium, the most common isotope of hydrogen. The term "hydron", endorsed by the IUPAC, includes cations of hydrogen regardless of their isotopic composition: thus it refers collectively to protons (1H+) for the protium isotope, deuterons (2H+ or D+) for the deuterium isotope, and tritons (3H+ or T+) for the tritium isotope. Unless there is a need to explicitly address issues of isotopic composition, the term "hydron" is not used, and to refer to H+
as such is considered pedantic. Nevertheless, H+
will be referred to as the "hydron", for the sake of consistency with the article title.

Hydron
Hydron.svg
Names
Systematic IUPAC name
Hydron[1] (substitutive)
Hydrogen(1+)[1] (additive)
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
UNII
Properties
H+
Thermochemistry
108.95 J K−1 mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Unlike most other ions, the hydron consists only of a bare atomic nucleus. The negatively charged counterpart of the hydron is the hydride anion, H
. In contrast to H+
, "hydride", not "protide", is the commonly used name for this species.

PropertiesEdit

Solute propertiesEdit

Other things being equal, compounds that readily donate hydrons (Brønsted acids, see below) are generally polar, hydrophilic solutes and are often soluble in solvents with high relative static permittivity (dielectric constants). Examples include organic acids like acetic acid (CH3COOH) or methanesulfonic acid (CH3SO3H). However, large nonpolar portions of the molecule may attenuate these properties. Thus, as a result of its alkyl chain, octanoic acid (C7H15COOH) is considerably less hydrophilic compared to acetic acid.

The unsolvated hydron (a completely free or "naked" hydrogen atomic nucleus) does not exist in the condensed (liquid or solid) phase. Although superacids are sometimes said owe their extraordinary hydron-donating power to the presence of "free hydrons", such a statement is highly misleading: even for a source of "free hydrons" like H
2
F+
, one of the superacidic cations present in the superacid fluoroantimonic acid (HF:SbF5), detachment of a free H+
still comes at an enormous energetic penalty on the order of several hundred kcal/mol. This effectively rules out the possibility of the free hydron being present in solution, even as a fleeting intermediate. For this reason, in liquid strong acids, hydrons are believed to diffuse by sequential transfer from one molecule to the next along a network of hydrogen bonds through what is known as the Grotthuss mechanism.[2]

AcidityEdit

The hydron ion can incorporate an electron pair from a Lewis base into the molecule by adduction:

[H]+
+ :L → [HL]+

Because of this capture of the Lewis base (L), the hydron ion has Lewis acidic character. In terms of Hard/Soft Acid Base (HSAB) theory, the bare hydron is an infinitely hard Lewis acid.

The hydron plays a central role in Brønsted–Lowry acid–base theory: a species that behaves as a hydron donor in a reaction is known as the Brønsted acid, while the species accepting the hydron is known as the Brønsted base. In the generic acid–base reaction shown below, HA is the acid, while B (shown with a lone pair) is the base:

HA + :B → [HB]+
+ :A

The hydrated form of the hydrogen cation, the hydronium (hydroxonium) ion H
3
O+
(aq), is a key object of Arrhenius' definition of acid. Other hydrated forms, the Zundel cation H
5
O+
2
, which is formed from a proton and two water molecules, and the Eigen cation H
9
O+
4
, which is formed from a hydronium ion and three water molecules, are theorized to play an important role in the diffusion of protons though an aqueous solution according to the Grotthuss mechanism. Although the ion H
3
O+
(aq) is often shown in introductory textbooks to emphasize that the hydron is never present as an unsolvated species in aqueous solution, it is somewhat misleading, as it oversimplifies infamously complex speciation of the solvated proton in water; the notation H+
(aq) is often preferred, since it conveys aqueous solvation while remaining noncommittal with respect to the number of water molecules involved.

Isotopes of hydronEdit

  1. Proton, having the symbol p or 1H+, is the +1 ion of protium, 1H.
  2. Deuteron, having the symbol 2H+ or D+, is the +1 ion of deuterium, 2H or D.
  3. Triton, having the symbol 3H+ or T+, is the +1 ion of tritium, 3H or T.

Other isotopes of hydrogen are too unstable to be relevant in chemistry.

History of the termEdit

The term "hydron" is recommended by IUPAC to be used instead of "proton" if no distinction is made between the isotopes proton, deuteron and triton, all found in naturally occurring undifferentiated isotope mixtures. The name "proton" refers to isotopically pure 1H+.[3] On the other hand, referring to the hydron as simply hydrogen ion is not recommended because hydrogen anions also exist.[4]

The term "hydron" was defined by IUPAC in 1988.[5][6] Traditionally, the term "proton" was and is used in place of "hydron".[citation needed] The latter term is generally only used in the context where comparisons between the various isotopes of hydrogen is important (as in the kinetic isotope effect or hydrogen isotopic labeling). Otherwise, referring to hydrons as protons is still considered acceptable, for example in such terms as protonation, deprotonation, proton pump, or proton channel. The transfer of H+
in an acid-base reaction is usually referred to as proton transfer. Acid and bases are referred to as proton donors and acceptors correspondingly.

99.9844% of natural hydrons (hydrogen nuclei) are protons, and the remainder (about 156 per million in sea water) are deuterons (see Deuterium), except for some very rare natural tritons (see Tritium).

See alsoEdit

ReferencesEdit

  1. ^ a b "hydron (CHEBI:15378)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.
  2. ^ [1] Archived 2011-09-27 at the Wayback Machine Computer modeling of proton-hopping in superacids.
  3. ^ Nomenclature of Inorganic Chemistry-IUPAC Recommendations 2005 [2] IR-3.3.2, p.48
  4. ^ Compendium of Chemical Terminology, 2nd edition McNaught, A.D. and Wilkinson, A. Blackwell Science, 1997 ISBN 0-86542-684-8, also online Archived 2005-12-12 at the Wayback Machine
  5. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "hydron". doi:10.1351/goldbook.H02904
  6. ^ Bunnet, J.F.; Jones, R.A.Y. (1968). "Names for hydrogen atoms, ions, and groups, and for reactions involving them (Recommendations 1988)" (PDF). Pure Appl. Chem. 60 (7): 1115–6. doi:10.1351/pac198860071115.