Issue 15, 2016

Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the “Rule-Breakers”(Cp* = η5-C5Me5)

Abstract

In an effort to synthesize supraicosahedral iridaboranes, pyrolysis of [Cp*IrCl2]2 with excess [BH3·THF] was carried out, and this synthesis afforded the isomeric iridaborane [(Cp*Ir)2B6H6] clusters 1 and 2. The geometry of 1 was determined to be dodecahedral, i.e., similar to that of [B8H8]2−, whereas 2 was found to exhibit a cluster shape that can be derived from a nine-vertex tricapped trigonal prism by removing one of the capped vertices. The calculation of a large HOMO–LUMO gap further rationalized the isocloso structures for these isomers.

Graphical abstract: Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the “Rule-Breakers”(Cp* = η5-C5Me5)

Supplementary files

Article information

Article type
Communication
Submitted
20 Nov 2015
Accepted
06 Jan 2016
First published
07 Jan 2016

Chem. Commun., 2016,52, 3199-3202

Author version available

Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the “Rule-Breakers”(Cp* = η5-C5Me5)

R. Borthakur, B. Mondal, P. Nandi and S. Ghosh, Chem. Commun., 2016, 52, 3199 DOI: 10.1039/C5CC09606E

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