Fluorescence resonance energy transfer between laser dyes in saponite dispersions

被引:19
作者
Czimerova, A.
Bujdak, J.
Iyi, N.
机构
[1] Slovak Acad Sci, Inst Inorgan Chem, SK-84536 Bratislava, Slovakia
[2] Natl Inst Mat Sci, AML, Tsukuba, Ibaraki 3050044, Japan
基金
日本学术振兴会;
关键词
fluorescence resonance energy transfer; smectite; laser dyes; ORGANIC-INORGANIC NANOCOMPOSITES; THIN SOLID FILMS; METHYLENE-BLUE; OPTICAL-PROPERTIES; CLAY; AGGREGATION; MONTMORILLONITE; ADSORPTION; SMECTITES; LAPONITE;
D O I
10.1016/j.jphotochem.2006.10.011
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
Fluorescence resonance energy transfer (FRET) between two cationic dyes, rhodamine 6G (R6G) and oxazine 4 (Ox4), in smectite (synthetic saponite, Sumecton) dispersions was studied. The interaction between smectite and the dyes was studied using visible (vis) and fluorescence spectroscopies. Only slight differences were observed between the vis spectra recorded in the presence and absence of the smectite. Due to low charge density of the smectite, the dyes did not form molecular aggregates in significant amounts. FRET was absent in the dye mixture solutions, but efficiently proceeded in aqueous dispersions with the smectite. The optimal conditions were observed for the concentration of 10(-5) M for both dye components. Lower concentrations of each dye probably led to larger intermolecular distances between the adsorbed dye cations, which reduced the efficiency of the energy transfer between the energy donor (R6G) and acceptor (Ox4). On the other hand, higher concentrations were not suitable for the FRET to run efficiently. Probably, self-quenching took place at high concentration of dye cations at interface. Formation of the H-type molecular assemblies with a sandwich-type association, which are very efficient quenchers, was not spectroscopically observed. No influence of the addition of the surfactant was observed in the systems with optimized conditions. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:160 / 166
页数:7
相关论文
共 35 条
[1]   ON THE AGGREGATION OF RHODAMINE-B IN ETHANOL [J].
ARBELOA, FL ;
OJEDA, PR ;
ARBELOA, IL .
CHEMICAL PHYSICS LETTERS, 1988, 148 (2-3) :253-258
[2]   Conventional and microwave-assisted crystallization inclusion of substituted rhodamine derivatives in AlPO4-5 [J].
Bockstette, M ;
Wohrle, D ;
Braun, I ;
Schulz-Ekloff, G .
MICROPOROUS AND MESOPOROUS MATERIALS, 1998, 23 (1-2) :83-96
[3]   Spectral properties, formation of dye molecular aggregates, and reactions in rhodamine 6G/layered silicate dispersions [J].
Bujdák, J ;
Iyi, N ;
Sasai, R .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (14) :4470-4477
[4]   The aggregation of methylene blue in montmorillonite dispersions [J].
Bujdák, J ;
Iyi, N ;
Fujita, T .
CLAY MINERALS, 2002, 37 (01) :121-133
[5]   Methylene blue interactions with reduced-charge smectites [J].
Bujdák, J ;
Janek, M ;
Madejová, J ;
Komadel, P .
CLAYS AND CLAY MINERALS, 2001, 49 (03) :244-254
[6]   Intercalation of rhodamine 6G and oxazine 4 into oriented clay films and their alignment [J].
Chen, GM ;
Iyi, NB ;
Sasai, R ;
Fujita, T ;
Kitamura, K .
JOURNAL OF MATERIALS RESEARCH, 2002, 17 (05) :1035-1040
[7]   Traditional and novel methods for estimating the layer charge of smectites [J].
Czimerova, A. ;
Bujdak, J. ;
Dohrmann, R. .
APPLIED CLAY SCIENCE, 2006, 34 (1-4) :2-13
[8]   The aggregation of thionine and methylene blue dye in smectite dispersion [J].
Czímerová, A ;
Bujdák, J ;
Gáplovsky, A .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2004, 243 (1-3) :89-96
[9]   Preferred formation of coplanar inclined fluorescent J-dimers in rhodamine 101 doped silica gels [J].
del Monte, F ;
Ferrer, ML ;
Levy, D .
LANGMUIR, 2001, 17 (16) :4812-4817
[10]  
ESTEVEZ MJT, 1993, LANGMUIR, V9, P3629