DUAL FLUORESCENCE OF 9-ANTHRYL-SUBSTITUTED OLIGOTHIOPHENES IN NONPOLAR ENVIRONMENT

被引：24

作者：

EMELE, P ^{[1
]}

MEYER, DU ^{[1
]}

HOLL, N ^{[1
]}

PORT, H ^{[1
]}

WOLF, HC ^{[1
]}

WURTHNER, F ^{[1
]}

BAUERLE, P ^{[1
]}

EFFENBERGER, F ^{[1
]}

机构：

[1] UNIV STUTTGART,INST ORGAN CHEM,W-7000 STUTTGART 80,GERMANY

来源：

CHEMICAL PHYSICS | 1994年 / 181卷 / 03期

关键词：

D O I：

10.1016/0301-0104(94)00007-7

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：

9-Anthryl-oligothiophenes (9A-T(n), n = 1-4) have been studied in n-hexane solution between helium and room temperature using absorption, fluorescence emission and excitation spectra and time resolved fluorescence measurements. These compounds are reference systems for studies on intramolecular energy and charge transfer in donor/acceptor-substituted conjugated chain molecules. The absorption spectra show contributions of both substituents anthracene and oligothiophene, but no additional bands due to mixed electronic states. Dual fluorescence is observed at T greater-than-or-equal-to 120 K for the compounds 9A-T(n) (n = 1-3), but not for 9A-T4. Time resolved spectroscopy reveals a dynamical coupling between the two emission components whose relative quantum yields are strongly temperature dependent. The occurrence of the dual fluorescence is explained by an intramolecular torsional motion between the two molecular subunits.

引用

页码：417 / 424

页数：8

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