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Guoqiao Lai

Researcher at Hangzhou Normal University

Publications -  177
Citations -  2961

Guoqiao Lai is an academic researcher from Hangzhou Normal University. The author has contributed to research in topics: Catalysis & Hydrosilylation. The author has an hindex of 29, co-authored 171 publications receiving 2579 citations. Previous affiliations of Guoqiao Lai include Zhejiang University of Technology & Chinese Ministry of Education.

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The recent synthesis and application of silicon-stereogenic silanes: A renewed and significant challenge in asymmetric synthesis

TL;DR: This critical review will focus on the recent exciting advances in the synthesis of silicon-stereogenic silane and outline the application of these chiral silanes in asymmetric synthesis.
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Tuning the solid-state luminescence of BODIPY derivatives with bulky arylsilyl groups: synthesis and spectroscopic properties.

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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Creep and recovery of polystyrene composites filled with graphene additives

TL;DR: In this paper, the authors investigated the creep and recovery behaviors of polystyrene (PS) composites filled with two-dimensional chemically reduced graphene oxide (CRGO) sheets and found that incorporation of CRGO into PS polymer is found to significantly improve the creep resistance and recovery properties.
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Ionic liquid functionalized silica gel: novel catalyst and fixed solvent

TL;DR: In this article, an imidazolium cation-based ionic liquid functionalized silica gel was used for cycloaddition of propylene oxide and carbon dioxide without any additional organic solvents.
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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.