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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Synthesis, characterization, photophysical and electrochemical properties of rhenium(I) tricarbonyl diimine complexes with triphenylphosphine ligand

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Author(s):
Goncalves, Marcia R. ; Frin, Karina P. M.
Total Authors: 2
Document type: Journal article
Source: Polyhedron; v. 132, p. 20-27, AUG 16 2017.
Web of Science Citations: 9
Abstract

In this work, the compounds fac-{[}ReL(CO)(3)(NN)](0/+1), NN = 1,10-phenanthroline, phen, 4,7-dimethyl-1,10-phenanthroline, Me(2)phen, or 4,7-dimethoxy-1,10-phenanthroline, (MeO)(2)phen, and L = Cl- or triphenylphosphine, PPh3, were synthetized and characterized by H-1 NMR, UV-vis and FTIR spectroscopies and their photophysical properties were investigated by steady-state and time-resolved emission spectroscopies. All complexes displayed strong absorption in the high energy UV-region assigned to intraligand transitions, ILNN, and the lower energy band was ascribed to a metal-to-ligand charge transfer, MLCTRe -> NN. The two electron donor groups attached to phen ligand shifted the emission maxima of the complexes to higher energy as the substituent becomes more electron donor, consequently the contribution of the (ILNN)-I-3 on the (MLCT)-M-3 emission becomes more evident. This effect is enhanced by coordinating the electron-withdrawing PPh3 ligand on Re(I) complexes (lambda(max) = 515 nm, phi = 13%, tau = 2.52 mu s for phen; lambda(max) = 512 nm, phi = 8.2%, tau = 2.00 mu s for Me(2)phen; lambda(max) = 478 and 506 nm, phi = 1.1%, tau = 1.12 mu s for (MeO)(2)phen). This interference is supported by the small shift of the emission maxima and two lifetimes in the mu s domain observed for substituted-phen complexes in PMMA films. The photophysics of Re (I) compounds reported herein provides new insights into the understanding of electron-donor groups on the phen ligand that are relevant to practical and fundamental development of photoinduced molecular devices. (C) 2017 Elsevier Ltd. All rights reserved. (AU)

FAPESP's process: 15/13149-8 - Polypyridynic rhenium(I) complexes: syntheses, investigation of photophysical properties and application as luminescent probes and/or therapeutic agents
Grantee:Karina Passalacqua Morelli Frin
Support type: Regular Research Grants