Time-resolved spectroscopy of 2-naphthol-triethylamine charge-transfer complexes in polar and non-polar solvents
✍ Scribed by P.B. Bisht; G.C. Joshi; H.B. Tripathi; D.D. Pant
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 439 KB
- Volume
- 142
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Hydrogen-bonded complexes of 2-naphthol-triethylamine have been studied in different polar and non-polar solvents. The ground-state equilibrium constants and the excited-state Stem-Volmer quenching rates have been calculated and both have been found to be greater in non-polar solvents. Decay-associated spectra and excitation spectra have shown that in non-polar solvents the exciplex is totally non-emitting while the ground-state hydrogen-bonded complex gives rise to a solvent-stabilised red-shifted ion-pair spectrum. In polar solvents, the usual excited-state proton transfer reaction takes place in which a risetime in the decay curve of solvent-separated ion pairs and a large red-shift in the spectrum are observed.
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## Abstract The resonance Raman and time‐resolved resonance Raman (TR^3^) spectra of ruthenium(II) complexes containing the asymmetric (RR)(5‐methyl‐2,2′‐bipyridine) ligand, Ru(5‐mmb), and its methyl‐deuterated analogue, Ru(5‐d~3~‐mmb), are reported. The spectra are compared to those of tris(2, 2′‐