2011年3月14日
Crystal structures and electronic properties of saddle-distorted and protonated phthalocyanines
Angewandte Chemie - International Edition
- ,
- ,
- ,
- 巻
- 50
- 号
- 12
- 開始ページ
- 2725
- 終了ページ
- 2728
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1002/anie.201006607
Protonation made easy: The formation and crystal structure determination of phthalocyanine protonated at the meso- and isoindole nitrogen atoms (see picture) are achieved by using the free base and a zinc complex of saddle-distorted octaphenylphthalocyanine, respectively. The saddle deformation alters the electronic structure of the phthalocyanine ring and facilitates its protonation. Copyright © 2011 WILEY-VCH Verlag GmbH &
Co. KGaA, Weinheim.
Co. KGaA, Weinheim.
- ID情報
-
- DOI : 10.1002/anie.201006607
- ISSN : 1433-7851
- ISSN : 1521-3773
- SCOPUS ID : 79952504417