Observation of photoluminescence in polypyrrole micelles

被引:33
作者
Jang, KS [1 ]
Ko, HC [1 ]
Moon, B [1 ]
Lee, H [1 ]
机构
[1] Sogang Univ, Dept Chem, Seoul 121742, South Korea
关键词
polypyrrole micelles; photoluminescence of polypyrrole; photoluminescence quenching in micelles; highly soluble polypyrrole; anionic surfactant-doped polypyrrole;
D O I
10.1016/j.synthmet.2005.01.013
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Photoluminescence (PL) was observed from micelles of polypyrrole without substituent groups. CHCI3 and CCI4 as well as 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) showed a typical fluorescence quenching behavior that can be observed when quencher molecules are added to a micellar solution of fluorescent material. At higher concentrations, the PL intensity decreased due to quenching in the aggregate phase and self-absorption. The PL intensity,varied depending upon the solvent in the order of dimethyl sulfoxide (DMSO) > N,N-dimethylformamide (DMF) > N-methyl-2-pyrrolidinone (NMP) > ethanol > toluene > tetrahydrofuran (THF). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 131
页数:5
相关论文
共 39 条
[21]   Intermolecular quenching of the second excited state of some aromatic molecules [J].
Lette, M. S. S. C. ;
Naqvi, K. Razt .
CHEMICAL PHYSICS LETTERS, 1969, 4 (01) :35-38
[22]   Polyaniline and polypyrrole: Where are we headed? [J].
MacDiarmid, AG .
SYNTHETIC METALS, 1997, 84 (1-3) :27-34
[23]  
NIGAM S, 1993, INDIAN J CHEM A, V32, P290
[24]   UV-Vis/NIR and transport studies of chemically synthesized soluble polypyrrole [J].
Oh, EJ ;
Jang, KS ;
Suh, JS ;
Kim, H ;
Kim, KH ;
Yo, CH ;
Joo, J .
SYNTHETIC METALS, 1997, 84 (1-3) :147-148
[25]   High molecular weight soluble polypyrrole [J].
Oh, EJ ;
Jang, KS ;
MacDiarmid, AG .
SYNTHETIC METALS, 2001, 125 (03) :267-272
[26]   Synthesis and characterization of high molecular weight, highly soluble polypyrrole in organic solvents [J].
Oh, EJ ;
Jang, KS .
SYNTHETIC METALS, 2001, 119 (1-3) :109-110
[27]   ELECTRONIC PROPERTIES OF N-HETEROAROMATICS .34. FLUORESCENCE OF ISOQUINOLINE DERIVATIVES WITH SPECIAL REFERENCE TO SOLVENT AND EXTERNAL HEAVY ATOM EFFECTS [J].
OKANO, T ;
MATSUMOTO, H .
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 1969, 89 (04) :510-+
[28]   FLUORESCENCE QUENCHING IN MICROHETEROGENEOUS MEDIA - A LABORATORY EXPERIMENT DETERMINING MICELLE AGGREGATION NUMBER [J].
PRIETO, MFR ;
RODRIGUEZ, MCR ;
GONZALEZ, MM ;
RODRIGUEZ, AMR ;
FERNANDEZ, JCM .
JOURNAL OF CHEMICAL EDUCATION, 1995, 72 (07) :662-663
[29]   Fluorescence quenching of aromatic amines by chloromethanes [J].
Saha, SK ;
Dogra, SK .
JOURNAL OF LUMINESCENCE, 1997, 75 (02) :117-125
[30]   FLUORESCENCE QUENCHING OF ULTRAVIOLET EXCITED AROMATIC SOLUTIONS BY CHLOROFORM AND SEVERAL RELATED CHLORINATED METHANES [J].
SAPERSTEIN, D ;
LEVIN, E .
JOURNAL OF CHEMICAL PHYSICS, 1975, 62 (09) :3560-3567