Triaryl Boron-Based A-π-A vs Triaryl Nitrogen-Based D-π-D Quadrupolar Compounds for Single- and Two-Photon Excited Fluorescence

Triaryl Boron-Based A-π-A vs Triaryl Nitrogen-Based D-π-D Quadrupolar Compounds for Single- and Two-Photon Excited Fluorescence

Three new A-π-A-type compounds with trivalent boron, protected by two mesityl groups, as electron acceptor have been synthesized and investigated together with their two diphenylamino-ended D-π-D analogues. These boranes exhibit large two-photon absorption cross sections and high fluorescence quantu...

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Veröffentlicht in:Organic letters 2004-08, Vol.6 (17), p.2933-2936
Hauptverfasser: Liu, Zhi-Qiang, Fang, Qi, Cao, Du-Xia, Wang, Dong, Xu, Gui-Bao
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container_issue 17
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container_title Organic letters
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creator Liu, Zhi-Qiang
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Cao, Du-Xia
Wang, Dong
Xu, Gui-Bao
description Three new A-π-A-type compounds with trivalent boron, protected by two mesityl groups, as electron acceptor have been synthesized and investigated together with their two diphenylamino-ended D-π-D analogues. These boranes exhibit large two-photon absorption cross sections and high fluorescence quantum yields.
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title Triaryl Boron-Based A-π-A vs Triaryl Nitrogen-Based D-π-D Quadrupolar Compounds for Single- and Two-Photon Excited Fluorescence
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