Pentaborane(11)

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Pentaborane(11)
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Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.038.447 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 242-307-4
UNII
  • InChI=1S/B5H11/c1-3-4-2-5(1,3)4/h5H,3-4H2,1-2H3
    Key: OPSKXWPMAKCNOG-UHFFFAOYSA-N
  • [BH3]1[BH2]2[BH]13[BH2]2[BH3]3
Properties
B5H11
Molar mass 65.14 g·mol−1
Melting point −123 °C (−189 °F; 150 K)
Boiling point 63 °C (145 °F; 336 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Pentaborane(11) is inorganic compound with the chemical formula B5H11. It is an obscure boron hydride cluster, especially relative to the heavily studied pentaborane(9) (B5H9). With two more hydrogen atoms than nido-pentaborane(9), pentaborane(11) is classified as an arachno- cluster. [1]

Synthesis

Like many boron hydride clusters, pentaborane(11) was originally obtained from the pyrolysis of diborane. A more systematic synthesis entails treatment of [B4H9] with boron tribromide. The Lewis acid abstracts hydride to give unstable B4H8, the precursor to B5H11: [2]

[B4H9] + BBr3 → B4H8 + HBBr3
2 B4H8 → B5H11 + "B3H5"

Related Research Articles

In chemistry, a hydride is formally the anion of hydrogen, H. The term is applied loosely. At one extreme, all compounds containing covalently bound H atoms are called hydrides: water (H2O) is a hydride of oxygen, ammonia is a hydride of nitrogen, etc. For inorganic chemists, hydrides refer to compounds and ions in which hydrogen is covalently attached to a less electronegative element. In such cases, the H centre has nucleophilic character, which contrasts with the protic character of acids. The hydride anion is very rarely observed.

Boranes

Boranes is the name given to compounds with the formula BxHy and related anions. Many such boranes are known. Most common are those with 1 to 12 boron atoms. Although they have few practical applications, the boranes exhibit structures and bonding that differs strongly from the patterns seen in hydrocarbons. Hybrids of boranes and hydrocarbons, the carboranes are also well developed.

Diborane Chemical compound

Diborane(6), generally known as diborane, is the chemical compound consisting of boron and hydrogen with the formula B2H6. It is a colorless, pyrophoric gas with a repulsively sweet odor. Synonyms include boroethane, boron hydride, and diboron hexahydride. Diborane is a key boron compound with a variety of applications. It has attracted wide attention for its electronic structure. Its derivatives are useful reagents.

Decaborane Chemical compound

Decaborane, also called decaborane(14), is the borane with the chemical formula B10H14. This white crystalline compound is one of the principal boron hydride clusters, both as a reference structure and as a precursor to other boron hydrides. It is toxic and volatile, with a foul odor.

Pentaborane(9) Chemical compound

Pentaborane(9) is an inorganic compound with the formula B5H9. It is one of the most common boron hydride clusters, although it is a highly reactive compound. Because of its high reactivity toward oxygen, it was once evaluated as rocket or jet fuel. Like many of the smaller boron hydrides, pentaborane is colourless, diamagnetic, and volatile. It is related to pentaborane(11) (B5H11).

Carborane Class of chemical compounds

Carboranes are electron-delocalized clusters composed of boron, carbon and hydrogen atoms. Like many of the related boron hydrides, these clusters are polyhedra or fragments of polyhedra. Carboranes are one class of heteroboranes.

Tetraborane Chemical compound

Tetraborane was the first boron hydride compound to be classified by Stock and Messenez in 1912 and was first isolated by Alfred Stock. It has a relatively low boiling point at 18 °C and is a gas at room temperature. Tetraborane gas is foul smelling and toxic.

In chemistry the polyhedral skeletal electron pair theory (PSEPT) provides electron counting rules useful for predicting the structures of clusters such as borane and carborane clusters. The electron counting rules were originally formulated by Kenneth Wade, and were further developed by others including Michael Mingos; they are sometimes known as Wade's rules or the Wade–Mingos rules. The rules are based on a molecular orbital treatment of the bonding. These rules have been extended and unified in the form of the Jemmis mno rules.

Triethylborane (TEB), also called triethylboron, is an organoborane (a compound with a B-C bond). It is a colorless pyrophoric liquid. Its chemical formula is (C2H5)3B, abbreviated Et3B. It is soluble in organic solvents tetrahydrofuran and hexane.

Marion Frederick Hawthorne was an inorganic chemist who made contributions to the chemistry of boron hydrides, especially their clusters.

Binary silicon-hydrogen compounds

Silanes are saturated chemical compounds with the empirical formula SixHy. They are hydrosilanes, a class of compounds that includes compounds with Si-H and other Si-X bonds. All contain tetrahedral silicon and terminal hydrides. They only have Si–H and Si–Si single bonds. The bond lengths are 146.0 pm for a Si–H bond and 233 pm for a Si–Si bond. The structures of the silanes are analogues of the alkanes, starting with silane, SiH
4
, the analogue of methane, continuing with disilane Si
2
H
6
, the analogue of ethane, etc. They are mainly of theoretical or academic interest.

Octadecaborane Chemical compound

Octadecaborane is an inorganic compound, a borane with chemical formula B18H22. It is a colorless flammable solid, like many higher boron hydrides. Although the compound has no practical applications, its structure is of theoretical and pedagogical interest.

Caesium dodecaborate Chemical compound

Caesium dodecaborate is an inorganic compound with the formula Cs2B12H12. It is a salt, with caesium cations and [B12H12]2− anions. This anion has been of great theoretical interest to the chemistry community.

Earl Muetterties

Earl Muetterties, was an American inorganic chemist born in Illinois, who is known for his experimental work with boranes, homogeneous catalysis, heterogeneous catalysis, fluxional processes in organometallic complexes and apicophilicity.

Trihydridoboron, also known as borane or borine, is an unstable and highly reactive molecule with the chemical formula BH
3
. The preparation of borane carbonyl, BH3(CO), played an important role in exploring the chemistry of boranes, as it indicated the likely existence of the borane molecule. However, the molecular species BH3 is a very strong Lewis acid. Consequently it is highly reactive and can only be observed directly as a continuously produced, transitory, product in a flow system or from the reaction of laser ablated atomic boron with hydrogen.

1,2-Dimethyldiborane Chemical compound

1,2-Dimethyldiborane is an organoboron compound with the formula [(CH3)BH2]2. Structurally, it is related to diborane, but with methyl groups replacing terminal hydrides on each boron. It is the dimer of methylborane, CH3BH2, the simplest alkylborane. 1,2-Dimethyldiborane can exist in a cis- and a trans arrangement. 1,2-Dimethyldiborane is an easily condensed, colorless gas that ignites spontaneously in air.

Methyldiborane Chemical compound

Methyldiborane, CH3B2H5, or monomethyldiborane is the simplest of alkyldiboranes, consisting of a methyl group substituted for a hydrogen in diborane. As with other boranes it exists in the form of a dimer with a twin hydrogen bridge that uses three-center two-electron bonding between the two boron atoms, and can be imagined as methyl borane (CH3BH2) bound to borane (BH3). Other combinations of methylation occur on diborane, including 1,1-dimethylborane, 1,2-dimethyldiborane, trimethyldiborane, tetramethyldiborane, and trimethylborane (which is not a dimer). At room temperature the substance is at equilibrium between these molecules.

Hexaborane(12) Chemical compound

Hexaborane(12) is an inorganic compound with the formula B6H12. It is an obscure member of the boranes. It is a colorless liquid that, like most boron hydrides, is readily hydrolyzed and flammable.

Ortho-carborane Chemical compound

Ortho-carborane is the organoboron compound with the formula C2B10H12. The prefix ortho is derived from ortho. It is the most prominent carborane. This derivative has been considered for a wide range of applications from heat-resistant polymers to medical applications. It is a colorless solid that melts, without decomposition, at 320 °C.

Octahydrotriborate Chemical compound

Octahydrotriborate is the boron hydride B3H8. It forms a variety of salts that are colorless and air-stable. The tetrabutylammonium salt is soluble in organic solvents such as acetonitrile and methylene chloride. The anion is an intermediate is the synthesis of various higher boron hydrides, such as pentaborane(9). B3H8 can be viewed as the conjugate base of triborane B3H9.

References

  1. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN   978-0-08-037941-8.
  2. Toft, Mark A.; Leach, J. B.; Himpsl, Francis L.; Shore, Sheldon G. (1982). "New, Systematic Syntheses of Boron Hydrides via Hydride ion Abstraction Reactions: Preparation of B2H6, B4H10, B5H11, and B10H14". Inorganic Chemistry. 21 (5): 1952–7. doi:10.1021/ic00135a048.