Photophysics of Singlet and Triplet Intraligand Excited States in [ReCl(CO)3(1-(2-pyridyl)-imidazo[1,5-α]pyridine)] Complexes
- 26 March 2014
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 136 (16) , 5963-5973
Abstract
Excited-state characters and dynamics of [ReCl(CO)3(3-R-1-(2-pyridyl)-imidazo[1,5-α]pyridine)] complexes (abbreviated ReGV-R, R = CH3, Ph, PhBut, PhCF3, PhNO2, PhNMe2) were investigated by pico- and nanosecond time-resolved infrared spectroscopy (TRIR) and excited-state DFT and TD-DFT calculations. Near UV excitation populates the lowest singlet state S1 that undergoes picosecond intersystem crossing (ISC) to the lowest triplet T1. Both states are initially formed hot and relax with ∼20 ps lifetime. TRIR together with quantum chemical calculations reveal that S1 is predominantly a ππ* state localized at the 1-(2-pyridyl)-imidazo[1,5-α]pyridine (= impy) ligand core, with impy → PhNO2 and PhNMe2 → impy intraligand charge-transfer contributions in the case of ReGV-PhNO2 and ReGV-PhNMe2, respectively. T1 is predominantly ππ*(impy) in all cases. It follows that excited singlet and corresponding triplet states have to some extent different characters and structures even if originating nominally from the same preponderant one-electron excitations. ISC occurs with a solvent-independent (CH2Cl2, MeCN) 20–30 ps lifetime, except for ReGV-PhNMe2 (10 ps in CH2Cl2, 100 ps in MeCN). ISC is 200–300 times slower than in analogous complexes with low-lying MLCT states. This difference is interpreted in terms of spin–orbit interaction and characters of orbitals involved in one-electron excitations that give rise to S1 and T1 states. ReGV-R present a unique case of octahedral heavy-metal complexes where the S1 lifetime is long enough to allow for separate spectroscopic characterization of singlet and triplet excited states. This study provides an insight into dynamics and intersystem crossing pathways of low-lying singlet and triplet excited states localized at bidentate ligands bound directly to a heavy metal atom. Rather long 1IL lifetimes indicate the possibility of photonic applications of singlet excited states.Keywords
Funding Information
- Science and Technology Facilities Council (CMSD 43)
- European Commission (CM1002)
- European Commission (CM1202)
- Queen Mary, University of London (NA)
- Ministry of Education, Youth and Sports (LD11086)
- Czech Science Foundation (P208/12/G016)
This publication has 85 references indexed in Scilit:
- Photophysical Properties of MM Quadruply Bonded Complexes Supported by Carboxylate Ligands, MM = Mo2, MoW, or W2Accounts of Chemical Research, 2012
- Spin–Orbit Treatment of UV–vis Absorption Spectra and Photophysics of Rhenium(I) Carbonyl–Bipyridine Complexes: MS-CASPT2 and TD-DFT AnalysisThe Journal of Physical Chemistry A, 2012
- On the interplay between charge, spin and structural dynamics in transition metal complexesDalton Transactions, 2012
- Luminescent Rhenium(I)-Dipyrrinato ComplexesInorganic Chemistry, 2011
- Electron delocalization in the S 1 and T 1 metal-to-ligand charge transfer states of trans -substituted metal quadruply bonded complexesProceedings of the National Academy of Sciences, 2011
- Phototriggering Electron Flow through ReI‐modified Pseudomonas aeruginosa AzurinsChemistry – A European Journal, 2011
- Spectroscopic and Computational Study on New Blue Emitting ReL(CO)3Cl Complexes Containing Pyridylimidazo[1,5‐a]pyridine LigandsEuropean Journal of Inorganic Chemistry, 2008
- Effect of the ligand-field strength on the radiative properties of the ligand-localized 3.pi..pi.* state of rhodium complexes with 1,10-phenanthroline: proposed role of dd statesThe Journal of Physical Chemistry, 1993
- Photochemical determination of the solubility of oxygen in various mediaTalanta, 1990
- Energy-adjustedab initio pseudopotentials for the second and third row transition elementsTheoretical Chemistry Accounts, 1990