Two-dimensional probing of ground-state vibrational dynamics in porphyrin molecules by fs-CARS

被引:42
作者
Heid, M
Schlücker, S
Schmitt, U
Chen, T
Schweitzer-Stenner, R
Engel, V
Kiefer, W
机构
[1] Univ Wurzburg, Inst Phys Chem, D-97074 Wurzburg, Germany
[2] Univ Puerto Rico, Dept Chem, San Juan, PR 00931 USA
关键词
D O I
10.1002/jrs.741
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
We report on spectrally dispersed femtosecond time-resolved coherent anti-Stokes Raman scattering (CARS) for the investigation of the electronic ground-state vibrational dynamics of porphyrin molecules in solution. The two-dimensional experimental data obtained in our measurements provide a detailed mapping of the large number of molecular vibrations in these systems, excited by broadband ultrashort laser pulses, and make a thorough interpretation of the complex signal structure possible. In particular, an analysis of the data by applying Fourier transform methods to the time domain signal allows a clear identification of the excited porphyrin normal modes when compared with results on the mode structure from spectrally resolved (cw) spectroscopy. Altogether the method is capable of yielding detailed information on the dephasing behavior and on the relative spectral positions of the excited vibrations at the same time. Three porphyrin systems, dissolved in dichloromethane, were investigated: magnesium octaethylporphyrin, magnesium tetraphenylporphyrin and the free-base porphyrin octaethylporphyrin. The measurements were performed in the spectral region of the ring vibrations of the porphyrin macrocycle. We also provide a discussion of the expected signals on a theoretical basis by deriving the CARS third-order non-linear polarization for these experiments. Copyright (C) 2001 John Wiley & Sons, Ltd.
引用
收藏
页码:771 / 784
页数:14
相关论文
共 47 条
[1]   Femtosecond laser-controlled selective excitation of vibrational modes on a multidimensional ground state potential energy surface [J].
Chen, T ;
Vierheilig, A ;
Waltner, P ;
Heid, M ;
Kiefer, W ;
Materny, A .
CHEMICAL PHYSICS LETTERS, 2000, 326 (5-6) :375-382
[2]   HIGH-PRECISION FEMTOSECOND CARS OF SIMPLE LIQUIDS [J].
FICKENSCHER, M ;
LAUBEREAU, A .
JOURNAL OF RAMAN SPECTROSCOPY, 1990, 21 (12) :857-861
[3]   STUDY OF THE EFFECTS OF SUBSTITUTION ON THE ABSORPTION SPECTRA OF PORPHIN [J].
GOUTERMAN, M .
JOURNAL OF CHEMICAL PHYSICS, 1959, 30 (05) :1139-1161
[4]   Spectrally resolved fs-CARS as a probe of the vibrational dynamics of a large polyatomic molecule: magnesium octaethylporphyrin [J].
Heid, M ;
Chen, T ;
Schmitt, U ;
Kiefer, W .
CHEMICAL PHYSICS LETTERS, 2001, 334 (1-3) :119-126
[5]   Ultrafast coherent control in the electronic ground state of a molecule [J].
Heid, M ;
Chen, T ;
Pausch, R ;
Schwoerer, H ;
Kiefer, W .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2000, 47 (4A) :637-645
[6]  
KAISER W, 1988, ULTRAFAST LASER PULS
[7]   FEMTOSECOND TIME-RESOLVED RESONANCE CARS THEORY [J].
KAMALOV, VF ;
SVIRKO, YP .
CHEMICAL PHYSICS LETTERS, 1992, 194 (1-2) :13-20
[8]   EXCITED TRIPLET-STATE RESONANCE RAMAN-SPECTRA OF MAGNESIUM, ZINC, AND PALLADIUM TETRAPHENYLPORPHINE [J].
KIM, D ;
TERNER, J ;
SPIRO, TG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (08) :2097-2099
[9]  
Knopp G, 2000, J RAMAN SPECTROSC, V31, P51, DOI 10.1002/(SICI)1097-4555(200001/02)31:1/2<51::AID-JRS504>3.0.CO
[10]  
2-R