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A series of asymmetrical phthalocyanines: synthesis and near infrared properties.


ABSTRACT: We report here the preparation of asymmetrical phthalocyanine dimers 1a-3a, which are endowed with novel charge transfer bands at 1,151-1,154 nm and strong NIR luminescences at 840-860 nm and 1,600-1,650 nm. Through H-bonding interaction, 1a-3a are inclined to self-assemble into hexrod nanotubes at the interface of CHCl? and CH?H. Our results provide further insights into the interaction in molecular dimers, and suggest that 1a-3a have potential application in magnets and supramolecular architectures.

SUBMITTER: Huang G 

PROVIDER: S-EPMC6270185 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

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A series of asymmetrical phthalocyanines: synthesis and near infrared properties.

Huang Guoqing G   Li Jianxi J   Cong Fangdi F   Li Chao C   Chu Xixi X   Meng Yanyan Y   Du Guotong G   Du Xiguang X  

Molecules (Basel, Switzerland) 20130419 4


We report here the preparation of asymmetrical phthalocyanine dimers 1a-3a, which are endowed with novel charge transfer bands at 1,151-1,154 nm and strong NIR luminescences at 840-860 nm and 1,600-1,650 nm. Through H-bonding interaction, 1a-3a are inclined to self-assemble into hexrod nanotubes at the interface of CHCl₃ and CH₃H. Our results provide further insights into the interaction in molecular dimers, and suggest that 1a-3a have potential application in magnets and supramolecular architec  ...[more]

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