Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/75673
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Title: Photosensitizer-free visible light-mediated gold-catalysed cis-difunctionalization of silyl-substituted alkynes
Authors: Deng, JR 
Chan, WC 
Lai, NCH 
Yang, B 
Tsang, CS 
Ko, BCB 
Chan, SLF 
Wong, MK 
Issue Date: 2017
Source: Chemical science, 2017, v. 8, no. 11, p. 7537-7544
Abstract: A new photosensitizer-free visible light-mediated gold-catalysed cis-difunctionalization reaction is developed. The reaction was chemoselective towards silyl-substituted alkynes with excellent regioselectivity and good functional group compatibility, giving a series of silyl-substituted quinolizinium derivatives as products. The newly synthesized fluorescent quinolizinium compounds, named JR-Fluor-1, possessed tunable emission properties and large Stokes shifts. With unique photophysical properties, the fluorophores have been applied in photooxidative amidations as efficient photocatalysts and cellular imaging with switchable subcellular localization properties.
Publisher: Royal Society of Chemistry
Journal: Chemical science 
ISSN: 2041-6520
EISSN: 2041-6539
DOI: 10.1039/c7sc02294h
Rights: © The Royal Society of Chemistry 2017
Open Access Article. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/).
The following publication Deng, J. R., Chan, W. C., Lai, N. C. H., Yang, B., Tsang, C. S., Ko, B. C. B., ... & Wong, M. K. (2017). Photosensitizer-free visible light-mediated gold-catalysed cis-difunctionalization of silyl-substituted alkynes. Chemical science, 8(11), 7537-7544 is available at https://doi.org/10.1039/c7sc02294h
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