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Bromide ion binding by a dinuclear gold(i) N-heterocyclic carbene complex: a spectrofluorescence and X-ray absorption spectroscopic study
Author(s) -
Louise E. Wedlock,
Jade B. Aitken,
Susan J. BernersPrice,
Peter J. Barnard
Publication year - 2012
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/c2dt31817b
Subject(s) - chemistry , extended x ray absorption fine structure , ion , absorption (acoustics) , fluorescence , carbene , bromide , crystallography , absorption spectroscopy , luminescence , binding energy , xanes , photochemistry , spectroscopy , inorganic chemistry , materials science , organic chemistry , physics , optoelectronics , quantum mechanics , nuclear physics , composite material , catalysis
Fluorescence and X-ray absorption spectroscopy were used to investigate the anion binding properties of a luminescent, dinuclear Au(I) N-heterocyclic carbene (NHC) complex ([1](2+)) with a short Au(I)···Au(I) contact. The addition of Br(-) ions to a DMSO solution of [1](PF(6))(2) caused a red-shift in the fluorescence emission band from 396 nm to 496 nm. Similarly, the addition of Br(-) ions to [1](PF(6))(2) caused a decrease in the energy of the Au L(3)-edge in the X-ray absorption spectrum, consistent with the formation of an association complex between the cation [1](2+) and Br(-) ions. Solution-based structural studies of the association complex were carried out using extended X-ray absorption fine structure (EXAFS) modelling of the Au(I)···Au(I) core of the cation. These studies indicate that the association complex results from Au(I)···Br(-) interactions, with the Br(-) ions occupying two partially occupied sites at ~2.9 and 3.9 Å from the Au(I) atoms.

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