L
Lizhi Gai
Researcher at Hangzhou Normal University
Publications - 48
Citations - 921
Lizhi Gai is an academic researcher from Hangzhou Normal University. The author has contributed to research in topics: BODIPY & Chemistry. The author has an hindex of 13, co-authored 36 publications receiving 737 citations. Previous affiliations of Lizhi Gai include Nanjing University & The Chinese University of Hong Kong.
Papers
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Journal ArticleDOI
Tuning the solid-state luminescence of BODIPY derivatives with bulky arylsilyl groups: synthesis and spectroscopic properties.
Hua Lu,Hua Lu,Qiuhong Wang,Lizhi Gai,Zhifang Li,Yuan Deng,Xu-Qiong Xiao,Guoqiao Lai,Zhen Shen +8 more
TL;DR: The chromophores are designed to prevent intermolecular π-π stacking interaction and enhance fluorescence in the solid state and show more pronounced increases in solid-state emission than triphenylsilylphenyl(ethynyl)-substituted BODIPYs.
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Ratiometric fluorescence chemodosimeters for fluoride anion based on pyrene excimer/monomer transformation
TL;DR: Two pyrene dimers containing an -O-Si-Si -Si-O- or -O/Si- O- linkage have been designed which exhibit ratiometric excimer/monomer emission upon fluoride anion induced Si-O bond cleavage and incorporation into water soluble polymeric nanoparticles enhances its intracellular uptake.
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Organosilicon compounds as fluorescent chemosensors for fluoride anion recognition
Lizhi Gai,Lizhi Gai,John Mack,Hua Lu,Hua Lu,Tebello Nyokong,Zhifang Li,Nagao Kobayashi,Zhen Shen +8 more
TL;DR: In this paper, the photophysical properties and electronic structures of organosilicon-based chemosensors are analyzed in depth with reference made to the results of molecular modeling calculation and possible future research directions are assessed.
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Synthesis and spectroscopic properties of bodipy dimers with effective solid-state emission
TL;DR: In this paper, Boron-dipyrromethenes (BODIPYs) dimers with phenyl and bulky triphenylsilylphenyl substituents were synthesized through oxidative self-coupling of the 2-position with FeCl3.
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New 2,6‐Distyryl‐Substituted BODIPY Isomers: Synthesis, Photophysical Properties, and Theoretical Calculations
Lizhi Gai,Lizhi Gai,John Mack,Hua Lu,Hiroko Yamada,Daiki Kuzuhara,Guoqiao Lai,Zhifang Li,Zhen Shen +8 more
TL;DR: Theoretical calculations provide strong evidence that styryl rotation and the formation of non-emissive charge-separated S1 states play a pivotal role in shaping the fluorescence properties of these dyes.