Issue 5, 2018

Approaching monocoordination at a silver(i) cation

Abstract

The recently reported bulky N-heterocyclic carbene ITr (ITr = [(HCNCPh3)2C:]) was found to stabilize low-coordinate Ag(I) environments. These electrophilic species were crystallographically identified as the weak solvates [(ITr)Ag(sol)]+ (sol = PhF, MesH or CH2Cl2) and as a solvent-free dimer [(ITr)Ag]22+. The highly electrophilic nature of the [(ITr)Ag]+ cation was further demonstrated by the calculation of a very high methyl ion affinity (MIA) and the synthesis of [(ITr)Ag(PCO)] which features substantial side-on electron donation from a P–C π bond to Ag.

Graphical abstract: Approaching monocoordination at a silver(i) cation

Supplementary files

Article information

Article type
Communication
Submitted
01 noy 2017
Accepted
14 dek 2017
First published
14 dek 2017

Chem. Commun., 2018,54, 483-486

Approaching monocoordination at a silver(I) cation

M. M. D. Roy, M. J. Ferguson, R. McDonald and E. Rivard, Chem. Commun., 2018, 54, 483 DOI: 10.1039/C7CC08418H

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