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In , a hydride is formally the of (H), a hydrogen ion with two electrons. In modern usage, this is typically only used for ionic bonds, but it is sometimes (and has been more frequently in the past) applied to all compounds containing H . In this broad and potentially archaic sense, (H2O) is a hydride of , is a hydride of , etc. In covalent compounds, it implies hydrogen is attached to a less . In such cases, the H centre has nucleophilic character, which contrasts with the protic character of acids. The hydride anion is very rarely observed.

Almost all of the elements form binary compounds with hydrogen, the exceptions being , exists as an ion. , is an ion, and the HNe excimer exists also. , exists as an ion. , exist as a cation. , , , , , and .

(1997). 9780750633659, Butterworth-Heinemann.
(2025). 9788126515547, Wiley. .
(2025). 9780471490395, Wiley. .
Exotic molecules such as positronium hydride have also been made.


Bonds
Bonds between hydrogen and the other elements range from being highly ionic to somewhat covalent. Some hydrides, e.g. , do not conform to classical electron counting rules and the bonding is described in terms of multi-centered bonds, whereas the interstitial hydrides often involve . Hydrides can be discrete , or , , monolayers, bulk metals (interstitial), or other materials. While hydrides traditionally react as or , some metal hydrides behave as hydrogen-atom donors and act as acids.


Applications
  • Hydrides such as sodium borohydride, lithium aluminium hydride, diisobutylaluminium hydride (DIBAL) and , are commonly used as in chemical synthesis. The hydride adds to an electrophilic center, typically unsaturated carbon.
  • Hydrides such as and potassium hydride are used as strong bases in organic synthesis. The hydride reacts with the weak releasing H2.
  • Hydrides such as are used as , i.e. drying agents, to remove trace water from organic solvents. The hydride reacts with water forming and salt. The dry solvent can then be distilled or vacuum transferred from the "solvent pot".
  • Hydrides are important in storage battery technologies such as nickel-metal hydride battery. Various metal hydrides have been examined for use as a means of hydrogen storage for -powered electric cars and other purposed aspects of a .
  • Hydride complexes are catalysts and catalytic intermediates in a variety of homogeneous and heterogeneous catalytic cycles. Important examples include , , , hydrodesulfurization catalysts. Even certain enzymes, the , operate via hydride intermediates. The energy carrier nicotinamide adenine dinucleotide reacts as a hydride donor or hydride equivalent.


Hydride ion
Free hydride anions exist only under extreme conditions and are not invoked for homogeneous solution. Instead, many compounds have hydrogen centres with hydridic character.

Aside from , the hydride ion is the simplest possible , consisting of two and a . Hydrogen has a relatively low electron affinity, 72.77 kJ/mol and reacts exothermically with protons as a powerful .

The low electron affinity of hydrogen and the strength of the H–H bond () means that the hydride ion would also be a strong


Types of hydrides
According to the general definition, every element of the (except some ) forms one or more hydrides. These substances have been classified into three main types according to the nature of their :
  • Ionic hydrides, which have significant character.
  • Covalent hydrides, which include the hydrocarbons and many other compounds which to hydrogen atoms.
  • Interstitial hydrides, which may be described as having .
While these divisions have not been used universally, they are still useful to understand differences in hydrides.


Ionic hydrides
These are stoichiometric compounds of hydrogen. Ionic or saline hydrides
(2025). 9783527306732
are composed of hydride bound to an electropositive metal, generally an or alkaline earth metal. The divalent such as and form compounds similar to those of heavier alkaline earth metals. In these materials the hydride is viewed as a . Saline hydrides are insoluble in conventional solvents, reflecting their non-molecular structures. Ionic hydrides are used as bases and, occasionally, as reducing in organic synthesis.
(1975). 9780471112808, John Wiley & Sons. .

Typical solvents for such reactions are . and other cannot serve as a medium for ionic hydrides because the hydride ion is a stronger base than and most anions. Hydrogen gas is liberated in a typical acid-base reaction.

Often alkali metal hydrides react with metal halides. Lithium aluminium hydride (often abbreviated as LAH) arises from reactions of with aluminium chloride.


Covalent hydrides
According to some definitions, covalent hydrides cover all other compounds containing hydrogen. Some definitions limit hydrides to hydrogen centres that formally react as hydrides, i.e. are nucleophilic, and hydrogen atoms bound to metal centers. These hydrides are formed by all the true non-metals (except zero group elements) and the elements like Al, Ga, Sn, Pb, Bi, Po, etc., which are normally metallic in nature, i.e., this class includes the hydrides of p-block elements. In these substances the hydride bond is formally a much like the bond made by a proton in a . This category includes hydrides that exist as discrete molecules, polymers or oligomers, and hydrogen that has been chem-adsorbed to a surface. A particularly important segment of covalent hydrides are complex metal hydrides, powerful soluble hydrides commonly used in synthetic procedures.

Molecular hydrides often involve additional ligands; for example, diisobutylaluminium hydride (DIBAL) consists of two aluminum centers bridged by hydride ligands. Hydrides that are soluble in common solvents are widely used in organic synthesis. Particularly common are sodium borohydride () and lithium aluminium hydride and hindered reagents such as DIBAL.


Interstitial hydrides or metallic hydrides
Interstitial hydrides most commonly exist within metals or alloys. They are traditionally termed "compounds" even though they do not strictly conform to the definition of a compound, more closely resembling common alloys such as steel. In such hydrides, hydrogen can exist as either atomic or diatomic entities. Mechanical or thermal processing, such as bending, striking, or annealing, may cause the hydrogen to precipitate out of solution by degassing. Their bonding is generally considered . Such bulk transition metals form interstitial binary hydrides when exposed to hydrogen. These systems are usually non-stoichiometric, with variable amounts of hydrogen atoms in the lattice. In materials engineering, the phenomenon of hydrogen embrittlement results from the formation of interstitial hydrides. Hydrides of this type form according to either one of two main mechanisms. The first mechanism involves the adsorption of dihydrogen, succeeded by the cleaving of the H-H bond, the delocalisation of the hydrogen's electrons, and finally the diffusion of the protons into the metal lattice. The other main mechanism involves the electrolytic reduction of ionised hydrogen on the surface of the metal lattice, also followed by the diffusion of the protons into the lattice. The second mechanism is responsible for the observed temporary volume expansion of certain electrodes used in electrolytic experiments.

absorbs up to 900 times its own volume of hydrogen at room temperatures, forming palladium hydride. This material has been discussed as a means to carry hydrogen for vehicular . Interstitial hydrides show certain promise as a way for safe . Neutron diffraction studies have shown that hydrogen atoms randomly occupy the octahedral interstices in the metal lattice (in an fcc lattice there is one octahedral hole per metal atom). The limit of absorption at normal pressures is PdH0.7, indicating that approximately 70% of the octahedral holes are occupied.Palladium hydride

Many interstitial hydrides have been developed that readily absorb and discharge hydrogen at room temperature and atmospheric pressure. They are usually based on compounds and solid-solution alloys. However, their application is still limited, as they are capable of storing only about 2 weight percent of hydrogen, insufficient for automotive applications.


Transition metal hydride complexes
Transition metal hydrides include compounds that can be classified as covalent hydrides. Some are even classified as interstitial hydrides and other bridging hydrides. Classical transition metal hydride feature a single bond between the hydrogen centre and the transition metal. Some transition metal hydrides are acidic, e.g., and . The anions potassium nonahydridorhenate and are examples from the growing collection of known molecular metal hydrides.A. Dedieu (Editor) Transition Metal Hydrides 1991, Wiley-VCH, Weinheim. As , hydride ligands are capable of bonding with positively polarized hydrogen centres. This interaction, called , is similar to , which exists between positively polarized protons and electronegative atoms with open lone pairs.


Isotopes
Hydrides containing protium are known as protides, hydrides containing are known as deuterides, and hydrides containing are known as tritides. Some deuterides, such as LiD, are important fusion fuels in thermonuclear weapons and useful moderators in .


Mixed anion compounds
Mixed anion compounds exist that contain hydride with other anions. These include boride hydrides, , , and others.


Appendix on nomenclature
Protide, deuteride and tritide are used to describe ions or compounds that contain enriched hydrogen-1, or , respectively.

In the classic meaning, hydride refers to any compound hydrogen forms with other elements, ranging over groups 1–16 (the binary compounds of hydrogen). The following is a list of the nomenclature for the hydride derivatives of main group compounds according to this definition:

According to the convention above, the following are "hydrogen compounds" and not "hydrides":

  • : water ("oxidane" when substituted; synonym: hydrogen oxide), hydrogen peroxide
  • : ("sulfane" when substituted)
  • : hydrogen selenide ("selane" when substituted)
  • : hydrogen telluride ("tellane" when substituted)
  • : hydrogen polonide ("polane" when substituted)
  • : hydrogen halides

Examples:

All metalloid hydrides are highly flammable. All solid non-metallic hydrides except are highly flammable. But when hydrogen combines with halogens it produces acids rather than hydrides, and they are not flammable.


Precedence convention
According to IUPAC convention, by precedence (stylized electronegativity), hydrogen falls between and elements. Therefore, we have NH3, "nitrogen hydride" (ammonia), versus H2O, "hydrogen oxide" (water). This convention is sometimes broken for polonium, which on the grounds of polonium's metallicity is often referred to as "polonium hydride" instead of the expected "hydrogen polonide".


See also


Bibliography
  • W. M. Mueller, J. P. Blackledge, G. G. Libowitz, Metal Hydrides, Academic Press, N.Y. and London, (1968)


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