A small series of boron‐dipyrromethene (BODIPY) dyes, characterized by the presence of multibranched fluorinated residues, were designed and synthesized. The dyes differ in both the position (para‐perfluoroalkoxy‐substituted phenyl ring or boron...
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https://www.riss.kr/link?id=O118663363
2019년
-
0947-6539
1521-3765
SCI;SCIE;SCOPUS
학술저널
9078-9087 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
A small series of boron‐dipyrromethene (BODIPY) dyes, characterized by the presence of multibranched fluorinated residues, were designed and synthesized. The dyes differ in both the position (para‐perfluoroalkoxy‐substituted phenyl ring or boron...
A small series of boron‐dipyrromethene (BODIPY) dyes, characterized by the presence of multibranched fluorinated residues, were designed and synthesized. The dyes differ in both the position (para‐perfluoroalkoxy‐substituted phenyl ring or boron functionalization) and number of magnetically equivalent fluorine atoms (27 or 54 fluorine atoms per molecule). Photophysical and crystallographic characterization of the synthesized BODIPYs was carried out to evaluate the effect of the presence of highly fluorinated moieties on the optical and morphological properties of such compounds.
Branching out: Four multibranched fluorinated boron‐dipyrromethene (BODIPY) dyes have been designed and prepared (see figure). Photophysical and crystallographic characterization of these BODIPYs was carried out to evaluate the effect of the presence of fluorinated moieties on the optical and morphological properties.