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September 12, 2007Journal of the American Chemical Society231 citations

Synthesis and Properties of 2,3,6,7-Tetraarylbenzo1,2-b:4,5-b‘difurans as Hole-Transporting Material

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HTHayato TsujiCMChikahiko MitsuiLILaurean Ilies

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Abstract

A new zinc-based annulation method produced regioselectively a variety of 2,3,6,7-tetraarylbenzo1,2- b:4,5- b ‘difurans in good yields. The organic electroluminescent devices using these tetraarylbenzodifurans as hole-transporting materials showed better performance than those using α-NPD, the current standard HTM. The hole drift mobility and the glass-transition temperatures of the tetraarylbenzodifurans were also found to be better than those of α-NPD.

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Cite This Study

Tsuji et al. (2007) studied this question.

synapsesocial.com/papers/6a5d26d73ce08021578a2c09https://doi.org/10.1021/ja074365w
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