Picosecond time-resolved resonance Raman probing of the light-switch states of Ru(Phen)(2)dppz (2+)
2001 (English)In: Journal of Physical Chemistry B, ISSN 1520-6106, E-ISSN 1520-5207, Vol. 105, no 50, 12653-12664 p.Article in journal (Refereed) Published
Picosecond time-resolved resonance Raman (picosecond-TR3) spectroscopy has been used to conduct an extensive photophysical characterization of the light- switch complex [Ru(phen)(2)dppz](2+) as a function of environment, in which studies have been carried out in aqueous and nonaqueous media and in DNA. The results are considered in rotation to a previous report describing environment-sensitive lowest triplet MLCT states. Vibrational marker features and enhancement patterns were used to determine the rapid progression (< 20 ps) between two triplet MLCT states in aqueous environment, followed by subnanosecond, nonradiative deactivation to the ground state. In nonaqueous environment, the long-lived, emissive triplet MLCT state is spectrally identified as the short-lived first triplet MLCT state observed in water, in agreement with the earlier proposed mechanism. The present data are shown to correlate well with previous nanosecond RR findings for the complex in each environment. Interestingly, a precursor state has been identified upon excitation in both nonaqueous solvent and in DNA, which precedes the triplet MLCT state, and the lifetime of which appears to be environment dependent. Observation of this state is discussed in relation to other recent femtosecond spectroscopic studies on this complex.
Place, publisher, year, edition, pages
2001. Vol. 105, no 50, 12653-12664 p.
excited-states, dipyridophenazine complexes, linear dichroism, binding modes, dna-binding, spectroscopy, ruthenium(ii), lambda-(2+), delta-(2+), relaxation
IdentifiersURN: urn:nbn:se:kth:diva-21199DOI: 10.1021/jp0127115ISI: 000172945700031OAI: oai:DiVA.org:kth-21199DiVA: diva2:339896
NoteQC 201005252010-08-102010-08-10Bibliographically approved