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|Title:||N-heterocyclic carbene Pt(ii) complexes from caffeine: Synthesis, structures and photoluminescent properties|
|Authors:||Hu, J.J. |
|Citation:||Hu, J.J., Bai, S.-Q., Yeh, H.H., Young, D.J., Chi, Y., Hor, T.S.A. (2011-05-07). N-heterocyclic carbene Pt(ii) complexes from caffeine: Synthesis, structures and photoluminescent properties. Dalton Transactions 40 (17) : 4402-4406. ScholarBank@NUS Repository. https://doi.org/10.1039/c0dt01380c|
|Abstract:||The caffeine-derived N-heterocyclic carbene (NHC) complex [Pt II(CN)(NHC)Cl] (CN = 2-phenylpyridine), 4 has the opposite stereochemistry and a shorter Pt-Ccarbene bond compared to that of an analogous benzimidazole-derived N,N-heterocyclic carbene (NNHC) Pt complex 2. These suggest a lower trans influence of pyridyl N compared to cyclometallated carbon and an increased Pt-NHC π-backbonding because of decreased π-donation resulting from conjugation to the electron deficient pyrimidine of caffeine. Complex 4 has a lower emission quantum yield (Φ) and is blue-shifted into the green region of the visible spectrum relative to non-carbene Pt(ii) cyclometalated complex 5. © 2011 The Royal Society of Chemistry.|
|Source Title:||Dalton Transactions|
|Appears in Collections:||Staff Publications|
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