Journal article
Cluster transformation of [Cu3(μ3-H)(μ3-BH4)((PPh2)2NH)3](BF4) to [Cu3(μ3-H)(μ2,μ1-S2CH)((PPh2)2NH)3](BF4): Via reaction with CS2. X-ray structural characterisation and reactivity of cationic clusters explored by multistage mass spectrometry and computational studies
HZ Ma, J Li, AJ Canty, RAJ O'Hair
Dalton Transactions | ROYAL SOC CHEMISTRY | Published : 2017
DOI: 10.1039/c7dt03510a
Abstract
The copper nanocluster [Cu3(μ3-H)(μ3-BH4)LPh3](BF4), 1a·BF4 (LPh = (PPh2)2NH = dppa), can potentially react with substrates at either the coordinated hydride or borohydride sites. Reaction of 1a·BF4 with CS2 has given rise to [Cu3(μ3-H)(μ2,μ1-S2CH)LPh3](BF4), (2a·BF4), which was structurally characterised using electrospray ionisation (ESI) with high-resolution mass spectrometry (HRMS), X-ray crystallography, NMR, IR and UV-Vis spectroscopy. The copper(i) atoms adopt a planar trinuclear Cu3 geometry coordinated on the bottom face by a μ3-hydride, on the top face by a μ2,μ1-dithioformate and surrounded by three bridging LPh ligands. Reaction of 1a·BF4 with elemental sulfur gives the known clu..
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Awarded by Australian Research Council
Funding Acknowledgements
We thank the Australian Research Council for financial support (DP150101388). The DFT calculations were carried out using the HPC facility of The University of Melbourne (punim0255) and at the National Computing Infrastructure.