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Journal ArticleDOI

Syntheses and properties of bis{bis(trimethylphosphine)tetrahydrodiboron}copper(1+) halide (halide = chloride, iodide) and x-ray crystal structure of the iodide

Mamoru Shimoi, +3 more
- 01 Jan 1990 - 
- Vol. 29, Iss: 4, pp 814-817
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TLDR
In this article, X-ray crystal structure analysis of the iodide showed that each ligand is coordinated to the copper atom through two vicinal hydrogen atoms and the copper atoms is ligated with four hydrogen atoms tetrahedrally.
Abstract
Chloride and iodide salts of bis{bis(trimethylphosphine)tetrahydrodiboron-H 1 ,H 2 } copper(I), [Cu{B 2 H 4 •2P(CH 3 ) 3 } 2 ]X (X=Cl, I), were prepared by the reactions of B 2 H 4 •2P(CH 3 ) 3 with the copper(I) halides. X-ray crystal structure analysis of the iodide shows that each ligand is coordinated to the copper atom through two vicinal hydrogen atoms and the copper atom is ligated with four hydrogen atoms tetrahedrally. Crystal data: monoclinic with the space group I2/a

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Journal ArticleDOI

Diboron(4) Compounds: From Structural Curiosity to Synthetic Workhorse

TL;DR: Although known for over 90 years, only in the past two decades has the chemistry of diboron(4) compounds been extensively explored and these compounds now feature prominently in both metal-catalyzed and metal-free methodologies for the formation of B-C bonds and other processes.
Journal ArticleDOI

Coordination Compounds of Monoborane−Lewis Base Adducts: Syntheses and Structures of [M(CO)5(η1-BH3·L)] (M = Cr, Mo, W; L = NMe3, PMe3, PPh3)

TL;DR: In this paper, the monoborane−Lewis base adduct coordinates to the metal center through a B−H−M three-center two-electron bond, which was confirmed by X-ray structural analyses of 1a, 2a, and 2b at low temperature.
Journal ArticleDOI

Investigation of the Stability of the M‐H‐B Bond in Borane σ Complexes [M(CO)5(η1‐BH2R⋅L)] and [CpMn(CO)2(η1‐BH2R⋅L)] (M=Cr, W; L=Tertiary Amine or Phosphine): Substituent and Lewis Base Effects

TL;DR: In this article, the influence of substituent and a Lewis base on boron upon the thermodynamic stability of metal complexes of borane-Lewis base adducts was investigated.
Journal ArticleDOI

Transition metal complexes of the chelating phosphine borane ligand Ph2PCH2Ph2P·BH3

TL;DR: All the new compounds (apart from the CO and MeCN adducts) have been characterised by X-ray crystallography and can be considered as being "operationally unsaturated", effectively acting as a source of 16-electron.
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