Picosecond emission anisotropy decays of dimethyl aminobenzonitrile

被引:17
作者
Fisz, JJ [1 ]
vanHoek, A [1 ]
机构
[1] AGR UNIV WAGENINGEN, DEPT MOL PHYS, NL-6703 HA WAGENINGEN, NETHERLANDS
关键词
INTRAMOLECULAR CHARGE-TRANSFER; P-SUBSTITUTED DIALKYLANILINES; ELECTRON-TRANSFER; EXCITED-STATES; FLUORESCENCE; TICT; MOLECULES; DYNAMICS;
D O I
10.1016/S0009-2614(97)00388-6
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
Picosecond polarized fluorescence experiments on DMABN (4-(dimethyl amino)benzonitrile) in polar solvents and toluene are reported. From the detected polarized fluorescence components emission anisotropy histograms are constructed and compared with the synthetic data simulated for the energy levels scheme in DMABN. For the short-wavelength emission of DMABN vibronic coupling between the close-lying S-1 and S-2 energy levels occurs and leads to a vibronically mixed polarization of the S-1 (F-B) fluorescence. Low initial values of the emission anisotropy decays for the long-wavelength (F-A) emission are observed. This observation can be explained by an assumption that the internal twisting of the amino group in DMABN changes the angular orientation of DMABN and by an assumption that the emission dipole moment in the F-A emission band is not parallel to the absorption dipole moment in the S-2 (L-1(a)) absorption band. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:432 / 442
页数:11
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