Photophysical properties of trans-platinum acetylide complexes featuring N-heterocyclic carbene ligands.

Abstract

A series of trans-N-heterocyclic carbene (NHC) platinum(ii) acetylide complexes of the form (ICy)2Pt(R)2 (where ICy = 1,3-bis-(cyclohexyl)imidazol-2-ylidene and R = 1-Ethynyl-4-(phenylethynyl)benzene (PE2), 2-(9,9-Diethyl-9H-fluoren-7-yl)benzo[d]thiazole (BTF), and 9,9-Diethyl-7-ethynyl-N,N-diphenyl-9H-fluoren-2-amine (DPAF), respectively), were synthesized via Hagihara reaction of the unprotected aryl-acetylide ligands with trans-(ICy)2PtCl2 () in 47-73% yield. Precursor was generated in a one-pot synthesis via formation of a silver carbene precursor followed by transmetallation, and was obtained in high yield (95%). The single-crystal X-ray structures of , were determined and analyzed. The photophysical properties of were compared to their respective tributyl phosphine (PBu3) analogues. The optical properties of the series were studied by UV-Vis spectroscopy, photoluminescence spectroscopy, nanosecond transient absorption spectroscopy, and open aperture nanosecond z-scan. Coupling of the organic chromophores to the platinum center affords efficient intersystem crossing as concluded by the complexes' low fluorescence quantum yields, efficient phosphorescence and intense T1 - Tn absorption. Open aperture z-scan with 606 nm, 10 ns laser pulses showed comparable optical attenuation relative to a standard sample of (PBu3)2Pt(DPAF)2 (). Pulse limiting was achieved via a dual-mechanism of two-photon absorption (2PA) coupled with excited-state absorption (ESA). TD-DFT Computations were also employed for to give greater insight into the nature of the singlet-singlet electronic transitions.

DOI: 10.1039/c4dt01520g

Cite this paper

@article{Winkel2014PhotophysicalPO, title={Photophysical properties of trans-platinum acetylide complexes featuring N-heterocyclic carbene ligands.}, author={Russell W. Winkel and Galyna G Dubinina and Khalil A Abboud and Kirk S Schanze}, journal={Dalton transactions}, year={2014}, volume={43 47}, pages={17712-20} }