Bromide ion binding by a dinuclear gold(I) N-heterocyclic carbene complex: a spectrofluorescence and X-ray absorption spectroscopic study

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Author(s)
Wedlock, Louise E
Aitken, Jade B
Berners-Price, Susan J
Barnard, Peter J
Griffith University Author(s)
Year published
2013
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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](PF6)2 caused a red-shift in the fluorescence emission band from 396 nm to 496 nm. Similarly, the addition of Br− ions to [1](PF6)2 caused a decrease in the energy of the Au L3-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 ...
View more >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](PF6)2 caused a red-shift in the fluorescence emission band from 396 nm to 496 nm. Similarly, the addition of Br− ions to [1](PF6)2 caused a decrease in the energy of the Au L3-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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View more >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](PF6)2 caused a red-shift in the fluorescence emission band from 396 nm to 496 nm. Similarly, the addition of Br− ions to [1](PF6)2 caused a decrease in the energy of the Au L3-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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Journal Title
Dalton Transactions
Volume
42
Issue
4
Funder(s)
ARC
Grant identifier(s)
DP0986318
Copyright Statement
© 2013 Royal Society of Chemistry. This is the author-manuscript version of this paper. Reproduced in accordance with the copyright policy of the publisher. Please refer to the journal website for access to the definitive, published version.
Subject
Inorganic chemistry
Bioinorganic chemistry
Theoretical and computational chemistry
Other chemical sciences