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Synthesis and photophysical properties of axially substituted silicon (IV) tetrapyrazinoporphyrazines

Authors
Park, Jong minJung, Chang YoungSong, Cheol JunJaung, Jae Yun
Issue Date
Dec-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Silicon tetrapyrazinoporphyrazine; Aggregation; Fluorescence quantum yield; Fluorescence quenching; Camphorquinone
Citation
INORGANIC CHEMISTRY COMMUNICATIONS, v.62, pp.64 - 66
Indexed
SCIE
SCOPUS
Journal Title
INORGANIC CHEMISTRY COMMUNICATIONS
Volume
62
Start Page
64
End Page
66
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/155727
DOI
10.1016/j.inoche.2015.10.015
ISSN
1387-7003
Abstract
We successfully synthesized non-aggregated silicon (IV) tetrapyrazinoporphyrazines (SiPz) bearing bornane groups at their peripheral positions. The UV-vis spectra of the SiPz complexes maintained a strong and sharp Q-band, which is an archetypal characteristic of non-aggregated phthalocyanines, in various organic solvents. In addition, the extreme red emission of SiPz complexes 4a-4c under visible light in a neutral solution condition was observed. However, the SiPz complex (4d) with axial aniline groups had very low fluorescence quantum yields due to the quenching ability of the aniline group.
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