New J. Chem., 2016, Advance Article
DOI: 10.1039/C5NJ03529EReceived11 Dec 2015,
Accepted11 Apr 2016
First published online 11 Apr 2016
triphenylphosphine complexes derived from methylated
5-trifluoromethyl-3-(2′-pyridyl)-1,2,4-triazole ligands has been
synthesized and well characterized. They all show an N2P2
distorted tetrahedral geometry and the methylated
5-trifluoromethyl-3-(2′-pyridyl)-1,2,4-triazole ligands display the
mono-anionic η2(N1,N2) and charge-neutral η2(N1,N4) chelating coordination modes, along with the 1,2,4-triazolyl ring inversion induced by the NH ↔ N− transformation. These Cu(I)
complexes are all emissive in solution and solid states at ambient
temperature, which can be well modulated by changing the methyl position
on the pyridyl ring and regulating the NH ↔ N−
conversion of the 1,2,4-triazolyl ring. It is also shown that the
deprotonation of 1,2,4-triazolyl-NH can markedly improve the
luminescence properties of Cu(I) complexes.
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