The low-energy S 1 → S n electronic transitions of 4,4 -bipyridine (44BPY) and the related resonance Raman intensities were analysed by ab initio calculation using the MCSCF method. This calculation is based on the previously optimized S 1 state geometry of 44BPY at the CIS level. The results are di
Resonance Raman and time-resolved resonance Raman studies of complexes of divalent ruthenium with bipyridine and 4,4′-bipyrimidine ligands
✍ Scribed by David J. Ma'nuel; Dennis P. Strommen; Anwar Bhuiyan; Milan Sykora; James R. Kincaid
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 319 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0377-0486
No coin nor oath required. For personal study only.
✦ Synopsis
Resonance Raman (RR) and time-resolved resonance Raman (TR3) spectra are reported for the complexes of divalent ruthenium with the ligands 4,4º-bipyrimidine (bpm) and 2,2º-bipyridine (bpy), i.e. and Ru(bpm) 3 2' Ground-state RR studies of the latter employing excitation with radiation of 413.1, 457.9 and Ru(bpy) 2 (bpm)2'. 514.5 nm permit the assignment of an electronic absorption band maximizing at 428.5 nm to a Ru(II)-to-bpy charge-transfer transition, while the band maximum at 516.0 nm is assigned to the Ru(II)-to-bpm charge-transfer band. The TR3 studies employing the 354.7 nm harmonic of a 10 ns pulsed Nd : YAG laser provide deÐnitive evidence for selective population of the bpm-localized excited state for the heteroleptic complex Ru(bpy) 2 (bpm)2'. 1997
📜 SIMILAR VOLUMES
The electronic absorption and resonance Raman spectra of a series of rhenium(I) and copper(I) complexes with substituted dipyrido[3,2-a : 2 ,3 -c]phenazine (dppz) ligands were investigated. The ligands were benzo[i ]dipyrido[3,2-a : 2 ,3 -c]phenazine, 11,12-dimethyldipyrido[3,2-a : 2 ,3 -c]phenazine
Microscopic solvation environments and ultrafast intermolecular energy transfer kinetics of trans-stilbene were studied in a sodium dodecyl sulfate (SDS) micellar solution and in a dodecane solution. The UV absorption spectrum showed no evidence of aggregate formation in the micellar solution. The a