| Literature DB >> 23566307 |
Jean-Luc Fillaut1, Huriye Akdas-Kilig, Edouard Dean, Camille Latouche, Abdou Boucekkine.
Abstract
A rational approach to luminescence turn-on sensing of cyanide by a dicyanovinyl-substituted acetylide Pt(II) complex, which primarily relies on the nucleophilic addition reaction of cyanide anions to the α-position of the dicyanovinyl group, is described. The strategy used for the design of this cyanide-selective sensor takes advantage of a switch of charge transfer from ML'CT to MLCT/L'LCT in this acetylide Pt(II) sensor. As a result, this chromophore that exhibits almost no basal luminescence displays observable changes in its UV-visible spectrum and acquires strong phosphorescence upon addition of cyanide anions. DFT computations reveal that the frontier molecular orbitals of the anionic system obtained after addition of CN(-) are drastically different from those of the neutral initial species. TD-DFT computations permitted a full assignment of the observed absorption bands and explained well the emissive properties of the species under consideration.Entities:
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Year: 2013 PMID: 23566307 DOI: 10.1021/ic302478e
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165