Detailed picosecond Kerr-gated time-resolved resonance Raman spectroscopy and time-resolved emission studies of merocyanine 540 in various solvents

被引:28
作者
Benniston, AC
Matousek, P
McCulloch, IE
Parker, AW
Towrie, M
机构
[1] Univ Newcastle Upon Tyne, Mol Photon Lab, Sch nat Sci Chem, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Rutherford Appleton Lab, CCLRC, Cent Laser Facil, Didcot OX11 0QX, Oxon, England
关键词
PHOTOPHYSICAL PROPERTIES; CYANINE DYES; DYNAMICS; SPECTRA; ISOMERIZATION; FLUORESCENCE; ABSORPTION; MECHANISM; PHOTOISOMERIZATION; POLARIZATION;
D O I
10.1021/jp027343z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
using the unique fluorescence rejection method of Kerr-gating, detailed picosecond time-resolved resonance Raman experiments have been performed on the highly fluorescent photodynamic therapy dye, Merocyanine 540 (MC540). This has enabled collection of the first-singlet trans excited resonance Raman spectra of this dye in a range of protic and aprotic solvents of varying viscosity and polarity, as well as an organized reverse micelle. The detailed vibrational spectra support the idea that protic solvents form a H-bonded cluster around the oxygen groups of the thiobarbiturate group, which lock the group in position and hinder its rotation. In the reverse micelle containing hexane/AOT and a water pool (omega(o) = 32) the dye is orientated to permit the thiobarbiturate group to interact with water pool molecules. Using the Kerr-gate setup, time-resolved emission spectra of MC540 were also recorded in various solvents. The dye undergoes fast vibrational cooling (2-10 ps), which can be related to the solvent's thermal diffusivity. A second slower process (20-100 ps) also occurs, which is viscosity dependent and is associated with structural relaxation of the polymethine unit within the dye.
引用
收藏
页码:4347 / 4353
页数:7
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