Tuning the color and excited state properties of the azulenic chromophore: NIR absorbing pigments and materials

被引:86
作者
Liu, RSH [1 ]
Asato, AE [1 ]
机构
[1] Univ Hawaii, Dept Chem, Honolulu, HI 96822 USA
基金
美国国家科学基金会;
关键词
azulene; S2-emission; bacteriorhodopsin; near infrared pigments; color-tuning; non-linear optical properties;
D O I
10.1016/j.jphotochemrev.2003.09.001
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
In this review, we summarize the work carried out at the University of Hawaii on the highly colored, non-alternant hydrocarbon azulene. Through systematic perturbation of the HOMO and LUMO molecular orbitals, we showed that the characteristic azure color can be changed in a manner that covers the entire visible spectrum based on this single chromophore. Some of the modified azulenes exhibit unusual excited state properties: reversal of energy gap of low lying excited states, unprecedented high fluorescence yield, and long fluorescence lifetime for an upper state in condensed media. Highly polarized polyene aldehydes attached to azulene at C-1 as a pi-electron donating end group have been successfully incorporated into bacterioopsin to generate NIR absorbing bacteriorhodopsin pigment analogs-the longest wavelength absorbing analog with gimel(max) = 830 nm. Azulene-containing donor-acceptor and symmetrical dye chromophores were synthesized and their excited state absorption spectra, and other properties determined. Non-linear optical properties were also examined. The azulenic dye chromophores are reverse saturable absorbers and are potentially useful for optical limiting applications. (C) 2003 Japanese Photochemistry Association. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:179 / 194
页数:16
相关论文
共 80 条
[1]   AZULENIC RETINOIDS AND THE CORRESPONDING BACTERIORHODOPSIN ANALOGS - UNUSUALLY RED-SHIFTED PIGMENTS [J].
ASATO, AE ;
LI, XY ;
MEAD, D ;
PATTERSON, GML ;
LIU, RSH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (20) :7398-7399
[2]   Azulene-containing donor-acceptor compounds as second-order nonlinear chromophores [J].
Asato, AE ;
Liu, RSH ;
Rao, VP ;
Cai, YM .
TETRAHEDRON LETTERS, 1996, 37 (04) :419-422
[3]   The use of prochiral centers for demonstrating asymmetric stacking in aggregates of azulenylazulenium cyanine dyes [J].
Asato, AE ;
Watanabe, DT ;
Liu, RSH .
ORGANIC LETTERS, 2000, 2 (17) :2559-2562
[4]  
ASATO AE, UNPUB
[5]   1-ALKYL-4-FLUORO-1,4-DIAZONIABICYCLO[2.2.2]OCTANE SALTS - A NOVEL FAMILY OF ELECTROPHILIC FLUORINATING AGENTS [J].
BANKS, RE ;
MOHIALDINKHAFFAF, SN ;
LAL, GS ;
SHARIF, I ;
SYVRET, RG .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (08) :595-596
[6]   The azulene S-1 state decays via a conical intersection: A CASSCF study with MMVB dynamics [J].
Bearpark, MJ ;
Bernardi, F ;
Clifford, S ;
Olivucci, M ;
Robb, MA ;
Smith, BR ;
Vreven, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (01) :169-175
[7]   ANOMALOUS LIGHT EMISSION OF AZULENE [J].
BEER, M ;
LONGUETHIGGINS, HC .
JOURNAL OF CHEMICAL PHYSICS, 1955, 23 (08) :1390-1391
[8]   Photoactivities of the red-shifted azulenic bacteriorhodopsin analogues [J].
Bell, JR ;
Muthyala, RS ;
Larsen, RW ;
Alam, M ;
Liu, RSH .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (28) :5481-5483
[9]  
BHAMERAM HE, 1994, CRC HDB ORG PHOTOCHE, P184
[10]   On the fluorescence anomaly of azulene [J].
Binsch, G. ;
Hexlbronner, E. ;
Jankow, R. ;
Schmidt, D. .
CHEMICAL PHYSICS LETTERS, 1967, 1 (04) :135-138