Beryllium hydride

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Beryllium hydride
Beryllium-hydride-3D-balls.png
Names
Other names
Beryllium dihydride
Beryllium hydride
Beryllane
Identifiers
7787-52-2 N
ChEBI CHEBI:33787 YesY
ChemSpider 17215712 YesY
Jmol 3D model Interactive image
PubChem 139073
  • InChI=1S/Be.2H YesY
    Key: RWASOQSEFLDYLC-UHFFFAOYSA-N YesY
  • InChI=1/Be.2H/rBeH2/h1H2
    Key: RWASOQSEFLDYLC-JICJMJRQAQ
  • [BeH2]
Properties
BeH2
Molar mass 11.03 g mol−1
Appearance amorphous white solid[1]
Density 0.65 g/cm3
Melting point 250 °C (482 °F; 523 K) decomposes
decomposes
Solubility insoluble in diethyl ether, toluene
Thermochemistry
30.124 J/mol K
Vapor pressure {{{value}}}
Related compounds
Other cations
lithium hydride, calcium hydride, boron hydrides
Related compounds
beryllium fluoride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Beryllium hydride (systematically named beryllium dihydride) is an inorganic compound with the chemical formula (BeH
2
)n (also written ([BeH
2
]
)n or BeH
2
). It is a colourless solid that is insoluble in solvents that do not decompose it.[2] Unlike the ionically bonded hydrides of the heavier Group 2 elements, beryllium hydride is covalently bonded[1] (three-center two-electron bond).

Synthesis

Unlike the other group 2 metals, beryllium does not react with hydrogen.[3] Instead, BeH2 is prepared from preformed beryllium(II) compounds. It was first synthesised in 1951 by treating dimethylberyllium, Be(CH3)2, with lithium aluminium hydride, LiAlH4.[4]

Purer BeH2 forms from the pyrolysis of di-tert-butylberyllium, Be(C(CH3)3)2 at 210 °C.[5]

A route to highly pure samples involve the reaction of triphenylphosphine, PPh3, with beryllium borohydride, Be(BH4)2:[1]

Be(BH4)2 + 2 PPh3 → 2 Ph3PBH3 + BeH2

Structure

BeH2 is usually formed as an amorphous white solid, but a hexagonal crystalline form with a higher density (~0.78 g cm−3) was reported,[6] prepared by heating amorphous BeH2 under pressure, with 0.5-2.5% LiH as a catalyst.

A more recent investigation found that crystalline beryllium hydride has a body-centred orthorhombic unit cell, containing a network of corner-sharing BeH4 tetrahedra, in contrast to the flat, hydrogen-bridged, infinite chains previously thought to exist in crystalline BeH2.[7]

Studies of the amorphous form also find that it consists of a network of corner shared tetrahedra.[8]

Chemical properties

Reaction with water and acids

Beryllium hydride reacts slowly with water but is rapidly hydrolysed by acid such as hydrogen chloride to form beryllium chloride.[3]

Reaction with Lewis bases

Beryllium hydride reacts with trimethylamine, N(CH3)3 to form a dimeric aduct, with bridging hydrides.[9] However with dimethylamine, HN(CH3)2 it forms a trimeric beryllium diamide, [Be(N(CH3)2)2]3 and hydrogen.[3] The reaction with lithium hydride where the hydride ion is the Lewis base, forms sequentially LiBeH3 and Li2BeH4.[3]

Dihydridoberyllium

Dihydridoberyllium is a related compound with the chemical formula BeH
2
(also written [BeH
2
]
). It is a gas that cannot persist undiluted. Unsolvated dihydridoberyllium will spontaneously autopolymerise to oligomers. Free molecular BeH2 produced by electrical discharge at high temperature has been confirmed as linear with a Be-H bond length of 133.376 pm. [10]

Chemical properties

In theory, the two-coordinate hydridoberyllium group (-BeH) in hydridoberylliums such as dihydridoberyllium can accept an electron-pair donating ligand into the molecule by adduction:[11]

[BeH
2
]
+ L → [BeH
2
L]

Because of this acceptance of the electron-pair donating ligand (L), dihydridoberyllium has Lewis-acidic-acidic character. Dihydridoberyllium can accept four two electron-pairs from ligands, as in the case of the tetrahydridoberyllate(2-) anion (BeH2−
4
).

References

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  2. Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
  3. 3.0 3.1 3.2 3.3 Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier ISBN 0-12-352651-5, p. 1048
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