Cationic Two-Photon Absorption Chromophores with Double- and Triple-Bond Cores in Symmetric/Asymmetric Arrangements

被引:40
作者
Kamada, Kenji [1 ]
Iwase, Yoichiro [2 ]
Sakai, Keiko [2 ]
Kondo, Koichi [2 ]
Ohta, Koji [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Photon Res Inst, Kansai Ctr, Osaka 5638577, Japan
[2] Ritsumeikan Univ, Dept Appl Chem, Fac Sci & Engn, Shiga 5258577, Japan
基金
日本学术振兴会;
关键词
OPTICAL-DATA STORAGE; PHOTOPHYSICAL PROPERTIES; CROSS-SECTION; FLUOROPHORES; FLUORESCENCE; ENHANCEMENT; DIACETYLENE; MOLECULES; DESIGN; NONLINEARITIES;
D O I
10.1021/jp901500v
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
Two-photon absorption (TPA) properties of a series of cationic, linear pi-conjugated systems with donor(D)/acceptor(A) substitution have been examined systematically in terms of the type and length of the pi-conjugation core and symmetric and asymmetric D/A-arrangement. The TPA spectra of the chromophores measured by the femtosecond open-aperture Z-scan method reveal that the double-bond core results in much more intense TPA than the triple-bond one, with a significant red shift of the TPA peak while the TPA becomes more intense as the chain is extended for the triple-bond core compounds with a little red shift. It is also found that the difference in the D/A-arrangement gives a small difference in the amplitude of the TPA spectrum although the spectral shapes differ considerably.
引用
收藏
页码:11469 / 11474
页数:6
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