New binding modes for CSe: coinage metal coordination to a tungsten selenocarbonyl complex
Author(s) -
Benjamin J. Frogley,
Anthony F. Hill,
Lachlan J. Watson
Publication year - 2019
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/c9dt02958c
Subject(s) - tungsten , electrophile , boron , metal , chemistry , ligand (biochemistry) , bridging (networking) , tungsten compounds , crystallography , inorganic chemistry , organic chemistry , computer science , computer network , biochemistry , receptor , catalysis
The new tungsten selenocarbonylate [NE 4 ][W([triple bond, length as m-dash]CSe)(CO) 2 (Tp*)] (Tp* = hydrotris(dimethylpyrazolyl)borate) reacts with group 11 reagents to provide σ-π or isoselenocarbonyl complexes of the form [WM(μ-CSe)(CO) 2 (PR 3 ) n (Tp*)] (M = Cu, Ag, Au; R = Ph, Cy; n = 1,3) depending on the phosphine stoichiometry or steric bulk. With [Cu(NCMe) 4 ]PF 6 and 1,4,7-trithiacyclononane ([9]aneS 3 ) however, the tetrametallic species [WCu 3 (μ-CSe)(CO) 2 ([9]aneS 3 ) 3 (Tp*)](PF 6 ) 2 is obtained in which one Cu coordinates to the W[triple bond, length as m-dash]C triple bond and two coordinate to the Se atom.
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