Cyclobuteno[60]fullerenes as Efficient n-Type Organic Semiconductors

被引:13
|
作者
Reboredo, Silvia [1 ]
Giron, Rosa M. [1 ]
Filippone, Salvatore [1 ]
Mikie, Tsubasa [2 ]
Sakurai, Tsuneaki [2 ]
Seki, Shu [2 ]
Martin, Nazario [1 ,3 ]
机构
[1] Univ Complutense Madrid, Ave Complutense S-N, E-28040 Madrid, Spain
[2] Kyoto Univ, Dept Mol Engn, Kyoto 6158510, Japan
[3] IMDEA Nanosci Inst, Campus Cantoblanco,C Faraday 9, Madrid 28049, Spain
基金
欧洲研究理事会;
关键词
alkynoates; allenoates; cyclobutene; electron mobility; fullerenes; PHOSPHINE-CATALYZED CYCLOADDITION; ELECTRON-DEFICIENT OLEFINS; CHARGE-CARRIER MOBILITY; FULLERENE DERIVATIVES; CHIRAL FULLERENES; ALLENOATES; ORGANOCATALYSIS; C-60; METHANOFULLERENE; INTERMEDIATE;
D O I
10.1002/chem.201602813
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclobuteno[3,4:1,2][60]fullerenes have been prepared in a straightforward manner by a simple reaction between [60]fullerene and readily available allenoates or alkynoates as organic reagents under basic and mild conditions. The chemical structure of the new modified fullerenes has been determined by standard spectroscopic techniques and confirmed by X-ray diffraction analysis. Some of these new fullerene derivatives exhibit a remarkable intrinsic electron mobility (determined by using flash-photolysis time-resolved microwave conductivity (FP-TRMC) measurements), which surpasses that of the well-known phenyl-C61-butyric acid methyl ester, thus behaving as promising n-type organic semiconductors.
引用
收藏
页码:13627 / 13631
页数:5
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