Electrochemistry, spectroscopy, and electrogenerated chemiluminescence of some star-shaped truxene-oligofluorene compounds

被引:45
|
作者
Omer, Khalid M.
Kanibolotsky, Alexander L.
Skabara, Peter J.
Perepichka, Igor F.
Bard, Allen J. [1 ]
机构
[1] Univ Texas, Ctr Electrochem, Dept Chem & Biochem, Austin, TX 78712 USA
[2] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
[3] Natl Acad Sci Ukraine, LM Litvinenko Inst Phys Organ & Coal Chem, UA-83114 Donetsk, Ukraine
[4] Univ Durham, Dept Chem, Durham DH1 3LE, England
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2007年 / 111卷 / 24期
基金
英国工程与自然科学研究理事会;
关键词
ATTAINING EXPONENTIAL CONVERGENCE; FINITE-DIFFERENCE EQUATIONS; OLIGOTHIOPHENE-FUNCTIONALIZED TRUXENE; UNEQUALLY SPACED GRIDS; LIGHT-EMITTING-DIODES; FLUX ERROR; MONODISPERSE OLIGOFLUORENES; DIGITAL SIMULATIONS; EMISSION PROPERTIES; AMORPHOUS MATERIALS;
D O I
10.1021/jp070765u
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
We report electrochemical studies, spectroscopy, and electrogenerated chemiluminescence (ECL) of four monodisperse star-shaped truxene core-oligofluorene compounds (T1-T4). All oligomers produced stable radical anions and radical cations and showed blue ECL by ion annihilation with an intensity that could be seen with the naked eye. ECL spectra showed that all ECL emissions were at the same position as the fluorescence emission, except for T1, the compound with the shortest fluorene arms that produced some longer wavelength emission in addition to that seen in the fluorescence spectrum. When tetra-n-butylammonium oxalate was used as a coreactant for T1, the emission was much weaker than that in ion annihilation with the same long-wavelength emission observed, making it unlikely that this emission can be ascribed to excimer formation. The ECL intensity of T4 was about 80% of the common blue ECL emitter, 9,10-diphenylanthracene (DPA), under similar conditions.
引用
收藏
页码:6612 / 6619
页数:8
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