作者: Páraic M. Keane , John M. Kelly
DOI: 10.1016/J.CCR.2018.02.018
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摘要: Abstract Recent advances in the use of transient absorption (TA) and time-resolved vibrational spectroscopies (TRIR TR3) to study both excited states reaction intermediates metal complexes porphyrins which intercalate into DNA are reviewed. A particularly well-studied class compounds, nicely illustrates comparative advantages these techniques, is that ruthenium dppz where complex might show light-switching or photo-oxidising behaviour depending on nature ancillary ligand. Comparative data Re- Cr-dppz also considered. In second part this review studies porphyrins, known DNA, considered with particular emphasis tetramethyl-pyridiniumporphyrins, photophysical metal-free various derivatives compared.