Intramolecular Charge Transfer of Curcumin and Solvation Dynamics of DMSO Probed by Time-Resolved Raman Spectroscopy

被引:9
作者
Jen, Myungsam [1 ]
Lee, Sebok [1 ]
Lee, Gisang [1 ]
Lee, Daedu [1 ]
Pang, Yoonsoo [1 ]
机构
[1] Gwangju Inst Sci & Technol, Dept Chem, 123 Cheomdangwagi Ro, Gwangju 61005, South Korea
基金
新加坡国家研究基金会;
关键词
intramolecular charge transfer; excited-state dynamics; solvation dynamics; femtosecond stimulated Raman spectroscopy; hydrogen bonding; PICOSECOND SPECTRAL RELAXATION; HYDROGEN-BONDED COMPLEXES; EXCITED-STATE; DIMETHYL-SULFOXIDE; ELECTRONIC EXCITATION; ULTRAFAST DYNAMICS; PROTON-TRANSFER; ATOM TRANSFER; SOLVENT; WATER;
D O I
10.3390/ijms23031727
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intramolecular charge transfer (ICT) of curcumin in dimethyl sulfoxide (DMSO) solution in the excited state was investigated by femtosecond electronic and vibrational spectroscopy. Excited-state Raman spectra of curcumin in the locally-excited and charge-transferred (CT) state of the S-1 excited state were separated due to high temporal (<50 fs) and spectral (<10 cm(-1)) resolutions of femtosecond stimulated Raman spectroscopy. The ultrafast (0.6-0.8 ps) ICT and subsequent vibrational relaxation (6-9 ps) in the CT state were ubiquitously observed in the ground- and excited-state vibrational modes of the solute curcumin and the nu(CSC) and nu(S=O) modes of solvent DMSO. The ICT of curcumin in the excited state was preceded by the disruption of the solvation shells, including the breakage of hydrogen bonding between curcumin and DMSO molecules, which occurs at the ultrafast (20-50 fs) time scales.
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页数:14
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