Separation of Photoactive Conformers Based on Hindered Diarylethenes: Efficient Modulation in Photocyclization Quantum Yields | Zendy

Li Wenlong | Zendy; Jiao Changhong | Zendy; Li Xin | Zendy; Xie Yongshu | Zendy; Nakatani Keitaro | Zendy; Tian He | Zendy; Zhu Weihong | Zendy

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Separation of Photoactive Conformers Based on Hindered Diarylethenes: Efficient Modulation in Photocyclization Quantum Yields

Author(s) -

Li Wenlong,

Jiao Changhong,

Li Xin,

Xie Yongshu,

Nakatani Keitaro,

Tian He,

Zhu Weihong

Publication year - 2014

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201310438

Subject(s) - diarylethene , intramolecular force , conformational isomerism , photochemistry , photochromism , bistability , quantum , chemistry , quantum efficiency , solvent , thermal , materials science , molecule , optoelectronics , organic chemistry , physics , quantum mechanics , meteorology

Endowing both solvent independency and excellent thermal bistability, the benzobis(thiadiazole)‐bridged diarylethene system provides an efficient approach to realize extremely high photocyclization quantum yields ( Φ o‐c , up to 90.6 %) by both separating completely pure anti‐parallel conformer and suppressing intramolecular charge transfer (ICT).

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