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  2. Boron hydride clusters - Wikipedia

    en.wikipedia.org/wiki/Boron_hydride_clusters

    Boron hydride clusters are compounds with the formula B x H y or related anions, where x ≥ 3. Many such cluster compounds are known. Common examples are those with 5, 10, and 12 boron atoms. Although they have few practical applications, the borane hydride clusters exhibit structures and bonding that differs strongly from the patterns seen in ...

  3. Boranes - Wikipedia

    en.wikipedia.org/wiki/Boranes

    This family of boron hydrides includes mono- and dialkylboranes. The simplest members readily engage in redistribution reactions: 2 BH 2 (CH 3) → BH(CH 3) 2 + 0.5 B 2 H 6. With bulky substituents, primary and secondary boranes are more readily isolable and even useful. Examples include thexylborane and 9-BBN. Almost all primary and secondary ...

  4. Group 13 hydride - Wikipedia

    en.wikipedia.org/wiki/Group_13_hydride

    Group 13 hydrides are chemical compounds containing group 13-hydrogen bonds (elements of group 13: boron, aluminium, gallium, indium, thallium, and nihonium). [ 1 ] Trihydrides

  5. Boron compounds - Wikipedia

    en.wikipedia.org/wiki/Boron_compounds

    Often the boron in borides has fractional oxidation states, such as −1/3 in calcium hexaboride (CaB 6). From the structural perspective, the most distinctive chemical compounds of boron are the hydrides. Included in this series are the cluster compounds dodecaborate (B 12 H 2− 12), decaborane (B 10 H 14), and the carboranes such as C 2 B 10 ...

  6. Borane - Wikipedia

    en.wikipedia.org/wiki/Borane

    The boron atom in BH 3 has 6 valence electrons. Consequently, it is a strong Lewis acid and reacts with any Lewis base ('L' in equation below) to form an adduct: [7] BH 3 + L → L—BH 3. in which the base donates its lone pair, forming a dative covalent bond. Such compounds are thermodynamically stable, but may be easily oxidised in air.

  7. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    Structure of a rare monomeric boron hydride, R = i-Pr. [4] The most-studied class of organoboron compounds has the formula BR n H 3−n. These compounds are catalysts, reagents, and synthetic intermediates. The trialkyl and triaryl derivatives feature a trigonal-planar boron center that is typically only weakly Lewis acidic.

  8. Boron group - Wikipedia

    en.wikipedia.org/wiki/Boron_group

    The elements in group 13 are also capable of forming stable compounds with the halogens, usually with the formula MX 3 (where M is a boron-group element and X is a halogen.) [14] Fluorine, the first halogen, is able to form stable compounds with every element that has been tested (except neon and helium), [15] and the boron group is no exception.

  9. Tetraborane - Wikipedia

    en.wikipedia.org/wiki/Tetraborane

    Tetraborane (systematically named arachno-tetraborane(10)) was the first boron hydride compound to be discovered. [2] It was classified by Alfred Stock and Carl Massenez in 1912 and was first isolated by Stock. [3] It has a relatively low boiling point at 18 °C and is a gas at room temperature. Tetraborane gas is foul smelling and toxic.