EXCIPLEX FORMATION DYNAMICS OF PHOTOEXCITED COPPER(II) TETRAKIS(4-N-METHYLPYRIDYL)PORPHYRIN WITH SYNTHETIC POLYNUCLEOTIDES PROBED BY TRANSIENT ABSORPTION AND RAMAN-SPECTROSCOPIC TECHNIQUES
Sc. Jeoung et al., EXCIPLEX FORMATION DYNAMICS OF PHOTOEXCITED COPPER(II) TETRAKIS(4-N-METHYLPYRIDYL)PORPHYRIN WITH SYNTHETIC POLYNUCLEOTIDES PROBED BY TRANSIENT ABSORPTION AND RAMAN-SPECTROSCOPIC TECHNIQUES, The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 101(30), 1997, pp. 5412-5417
To elucidate the interaction mechanism of water-soluble copper(II) tet
rakis(4-N-methylpyridyl)porphyrin (Cu-II- (TMpy-P4)) with synthetic po
lynucleotides such as poly(dA-dT)(2) and poly(dC-dC)(2), the exciplex
formation dynamics of photoexcited Cu-II(TMpy-P4) with added polynucle
otides have been investigated by using femtosecond transient absorptio
n as well as transient Raman spectroscopic methods. The nanosecond tra
nsient Raman spectra of Cu-II(TMpy-P4) mixed with poly(dA-dT)(2) clear
ly demonstrate the exciplex formation between photoexcited Cu-II(TMpy-
P4) and poly(dA-dT)(2). On the other hand, the exciplex formation of p
hotoexcited Cu-II(TMpy-P4) with poly(dG-dC)(2) is not so manifest as c
ompared with that mixed with poly(dA-dT)(2). The transient absorption
of Cu-II(TMpy-P4) mixed with poly(dG-dC)(2) exhibits a rise component
of 1.3 ps in addition to the very slow decay component (tau similar to
22 ns). This observation is quite different from that of Cu-II(TMpy-P
4) in aqueous solution or Cu-II(TMpy-P4) mixed with poly(dA-dT)(2), be
cause the exciplex formed in poly(dG-dC)(2), if any, is so short-lived
that it returns quickly back to four-coordinate Cu-II(TMpy-P4) interc
alated at poly(dG-dC)(2), which blocks the axial coordination by water
molecules and consequently gives rise to a long lifetime (tau similar
to 22 ns).