Fourier analysis of the femtosecond hyper-Rayleigh scattering signal from ionic fluorescent hemicyanine dyes

被引:75
作者
Clays, K
Wostyn, K
Olbrechts, G
Persoons, A
Watanabe, A
Nogi, K
Duan, XM
Okada, S
Oikawa, H
Nakanishi, H
Vogel, H
Beljonne, D
Brédas, JL
机构
[1] Univ Louvain, Dept Chem, Lab Chem & Biol Dynam, Ctr Res Mol Elect & Photon, B-3001 Louvain, Belgium
[2] Tohoku Univ, Inst Chem React Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
[3] Univ Mons, Ctr Res Mol Elect & Photon, Lab Chem Novel Mat, B-7000 Mons, Belgium
[4] Univ Arizona, Dept Chem, Tucson, AZ 85721 USA
[5] Univ Arizona, Ctr Opt Sci, Tucson, AZ 85721 USA
关键词
D O I
10.1364/JOSAB.17.000256
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
A series of five fluorescent and ionic dimethylamino stilbazolium homologues with increasing conjugation length (from ethenyl to decapentaenyl) is investigated by high-frequency, amplitude-modulated femtosecond hyper-Rayleigh scattering at 1300 nm. A hyperpolarizability value that is not overestimated by the presence of a multiphoton fluorescence contribution is obtained from the Fourier analysis of the hyper-Rayleigh scattering signal. The demodulation curve (decrease of Fourier amplitude versus modulation frequency) is characterized by both the hyperpolarizability value and the fluorescence decay parameters. The fluorescence decay parameters are accurately determined independently by single-photon counting. A detailed analysis of the fluorescence decay parameters from the hyper-Rayleigh scattering demodulation curve and of their relation to the fluorescence decay parameters obtained from single-photon counting experiments is presented. The inherent hyperpolarizability value for these chromophores shows a maximum of (2045 +/- 35) x 10(-30) esu or (760 +/- 13) x 10(-50) C-3 m(3) J(-2) for the hexatrienyl conjugation length. A comparison with theoretical calculations suggests the importance of trans-cis isomerization in the excited state. (C) 2000 Optical Society of America [S0740-3224(00)00102-8].
引用
收藏
页码:256 / 265
页数:10
相关论文
共 28 条
  • [1] INSTRUMENTAL AND ANALYSIS IMPROVEMENTS IN MULTIFREQUENCY PHASE FLUOROMETRY
    CLAYS, K
    JANNES, J
    ENGELBORGHS, Y
    PERSOONS, A
    [J]. JOURNAL OF PHYSICS E-SCIENTIFIC INSTRUMENTS, 1989, 22 (05): : 297 - 305
  • [2] HYPER-RAYLEIGH SCATTERING IN SOLUTION
    CLAYS, K
    PERSOONS, A
    [J]. PHYSICAL REVIEW LETTERS, 1991, 66 (23) : 2980 - 2983
  • [3] HYPER-RAYLEIGH SCATTERING IN SOLUTION
    CLAYS, K
    PERSOONS, A
    [J]. REVIEW OF SCIENTIFIC INSTRUMENTS, 1992, 63 (06) : 3285 - 3289
  • [4] Enhancement of the molecular hyperpolarizability by a supramolecular amylose-dye inclusion complex, studied by hyper-Rayleigh scattering with fluorescence suppression
    Clays, K
    Olbrechts, G
    Munters, T
    Persoons, A
    Kim, OK
    Choi, LS
    [J]. CHEMICAL PHYSICS LETTERS, 1998, 293 (5-6) : 337 - 342
  • [5] Clays K., 1994, ADV CHEM PHYS, V85, P455
  • [6] THE DEVELOPMENT AND USE OF QUANTUM-MECHANICAL MOLECULAR-MODELS .76. AM1 - A NEW GENERAL-PURPOSE QUANTUM-MECHANICAL MOLECULAR-MODEL
    DEWAR, MJS
    ZOEBISCH, EG
    HEALY, EF
    STEWART, JJP
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (13) : 3902 - 3909
  • [7] DUAN XM, 1994, P SOC PHOTO-OPT INS, V2143, P41, DOI 10.1117/12.173833
  • [8] LENGTH DEPENDENCE OF THE 2ND-ORDER OPTICAL NONLINEARITY IN CONJUGATED HYDROCARBONS
    DULCIC, A
    FLYTZANIS, C
    TANG, CL
    PEPIN, D
    FETIZON, M
    HOPPILLIARD, Y
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1981, 74 (03) : 1559 - 1563
  • [9] THE DETERMINATION OF FIRST HYPERPOLARIZABILITIES-BETA USING HYPER-RAYLEIGH SCATTERING - A CAVEAT
    FLIPSE, MC
    DEJONGE, R
    WOUDENBERG, RH
    MARSMAN, AW
    VANWALREE, CA
    JENNESKENS, LW
    [J]. CHEMICAL PHYSICS LETTERS, 1995, 245 (2-3) : 297 - 303
  • [10] THE BACTERIORHODOPSIN CHROMOPHORE RETINAL AND DERIVATIVES - AN EXPERIMENTAL AND THEORETICAL INVESTIGATION OF THE 2ND-ORDER OPTICAL-PROPERTIES
    HENDRICKX, E
    CLAYS, K
    PERSOONS, A
    DEHU, C
    BREDAS, JL
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (12) : 3547 - 3555