Evaluation of sensitizing ability of barbiturate-functionalized non-ionic cyanine dyes; application for photoinduced radical generation system initiated by near IR light

被引:39
作者
Karatsu, T
Yanai, M
Yagai, S
Mizukami, J
Urano, T
Kitamura, A
机构
[1] Chiba Univ, Dept Mat Technol, Fac Engn, Inage Ku, Chiba 2638522, Japan
[2] Mitsubishi Chem Corp, Res Ctr, Aoba Ku, Yokohama, Kanagawa 2278502, Japan
关键词
photopolymerization; cyanine dye; near IR; photoinduced electron transfer;
D O I
10.1016/j.jphotochem.2004.08.010
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 [物理化学]; 081704 [应用化学];
摘要
The sensitizing abilities of near infrared (near IR)-absorbing ionic (D1) and non-ionic (D2 and D3) cyanine dyes in a photoinduced radical polymerization system were evaluated. The solubility in an organic solvent of non-ionic cyanine dyes is much higher than that of an ionic cyanine dye. The photoinduced radical polymerization system consists of a sensitizing dye (D1-D3), 2,4,6-tris(trichloromethyl)-s-triazine (TCT, as a radical genetrator), and a poly-functional acrylate monomer (DPHA) in the binder polymer. All dyes showed a sensitizing ability in the photoinduced radical polymerization systems by near IR light. Non-ionic cyanine dyes, D2 and D3, showed a higher sensitizing ability than D1. From the IR and UV-vis studies, it was revealed that the high sensitizing ability of D2 and D3 is a result of an interaction between the dye and TCT in the polymer matrices, promoting the electron-transfer from the dyes to the TCT. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 129
页数:7
相关论文
共 44 条
[1]
Photoisomerization of sterically hindered merocyanine dyes [J].
Benniston, AC ;
Harriman, A ;
McAvoy, C .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1997, 93 (20) :3653-3662
[2]
Large quadratic hyperpolarizabilities with donor-acceptor polyenes exhibiting optimum bond length alternation: Correlation between structure and hyperpolarizability [J].
BlanchardDesce, M ;
Alain, V ;
Bedworth, PV ;
Marder, SR ;
Fort, A ;
Runser, C ;
Barzoukas, M ;
Lebus, S ;
Wortmann, R .
CHEMISTRY-A EUROPEAN JOURNAL, 1997, 3 (07) :1091-1104
[3]
EXPERIMENTAL DEMONSTRATION OF THE DEPENDENCE OF THE 1ST HYPERPOLARIZABILITY OF DONOR-ACCEPTOR-SUBSTITUTED POLYENES ON THE GROUND-STATE POLARIZATION AND BOND-LENGTH ALTERNATION [J].
BOURHILL, G ;
BREDAS, JL ;
CHENG, LT ;
MARDER, SR ;
MEYERS, F ;
PERRY, JW ;
TIEMANN, BG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (06) :2619-2620
[4]
ELECTRON-TRANSFER REACTIONS IN CYANINE BORATE ION-PAIRS - PHOTOPOLYMERIZATION INITIATORS SENSITIVE TO VISIBLE-LIGHT [J].
CHATTERJEE, S ;
GOTTSCHALK, P ;
DAVIS, PD ;
SCHUSTER, GB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (07) :2326-2328
[5]
PHOTOCHEMISTRY OF CARBOCYANINE ALKYLTRIPHENYLBORATE SALTS - INTRA-ION-PAIR ELECTRON-TRANSFER AND THE CHEMISTRY OF BORANYL RADICALS [J].
CHATTERJEE, S ;
DAVIS, PD ;
GOTTSCHALK, P ;
KURZ, ME ;
SAUERWEIN, B ;
YANG, XQ ;
SCHUSTER, GB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (17) :6329-6338
[6]
REAL-TIME KINETIC-STUDY OF LASER-INDUCED POLYMERIZATION [J].
DECKER, C ;
MOUSSA, K .
MACROMOLECULES, 1989, 22 (12) :4455-4462
[7]
Decker C, 1997, J APPL POLYM SCI, V65, P833, DOI 10.1002/(SICI)1097-4628(19970801)65:5<833::AID-APP1>3.0.CO
[8]
2-O
[9]
Eaton D.F., 1986, ADV PHOTOCHEM, V13, P427
[10]
NEAR-INFRARED ABSORBING DYES [J].
FABIAN, J ;
NAKAZUMI, H ;
MATSUOKA, M .
CHEMICAL REVIEWS, 1992, 92 (06) :1197-1226