tetrabenzoporphine

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CAS: 52952-31-5
MF: C36H22N4
MW: 510.58668
Synonyms: tetrabenzoporphine

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Craig J. Hawker

University of California
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Thuc-Quyen Nguyen

University of California
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Eiichi Nakamura

The University of Tokyo
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Co-reporter: Yutaka Matsuo, Ying Zhang, Iwao Soga, Yoshiharu Sato, Eiichi Nakamura
pp: 2240-2242
Publication Date(Web):27 April 2011
DOI: 10.1016/j.tetlet.2011.01.031
An AlCl3-mediated Friedel–Crafts reaction of arenes with C60 affords two-fold hydroarylated compounds, C60Ar2H2, which upon deprotonation with tBuOK and oxidation with CuBr·SMe2 yield 1,4-diaryl[60]fullerenes, C60Ar2 (Ar = Ph, 4-Me-C6H4, 3,4-Me2-C6H3, and 4-Ph-C6H4) in good yield. A solution-processed, thin-film organic photovoltaic device using C60(4-PhC6H4)2 as electron acceptor material showed a 2.3% power conversion efficiency.Image for unlabelled figure

Masaki Matsuda

Kumamoto University
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Yutaka Matsuo

The University of Tokyo
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Co-reporter: Yutaka Matsuo, Ying Zhang, Iwao Soga, Yoshiharu Sato, Eiichi Nakamura
pp: 2240-2242
Publication Date(Web):27 April 2011
DOI: 10.1016/j.tetlet.2011.01.031
An AlCl3-mediated Friedel–Crafts reaction of arenes with C60 affords two-fold hydroarylated compounds, C60Ar2H2, which upon deprotonation with tBuOK and oxidation with CuBr·SMe2 yield 1,4-diaryl[60]fullerenes, C60Ar2 (Ar = Ph, 4-Me-C6H4, 3,4-Me2-C6H3, and 4-Ph-C6H4) in good yield. A solution-processed, thin-film organic photovoltaic device using C60(4-PhC6H4)2 as electron acceptor material showed a 2.3% power conversion efficiency.Image for unlabelled figure