Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/75673
DC Field | Value | Language |
---|---|---|
dc.contributor | Department of Applied Biology and Chemical Technology | - |
dc.contributor | Chinese Mainland Affairs Office | - |
dc.creator | Deng, JR | - |
dc.creator | Chan, WC | - |
dc.creator | Lai, NCH | - |
dc.creator | Yang, B | - |
dc.creator | Tsang, CS | - |
dc.creator | Ko, BCB | - |
dc.creator | Chan, SLF | - |
dc.creator | Wong, MK | - |
dc.date.accessioned | 2018-05-10T02:54:21Z | - |
dc.date.available | 2018-05-10T02:54:21Z | - |
dc.identifier.issn | 2041-6520 | - |
dc.identifier.uri | http://hdl.handle.net/10397/75673 | - |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.rights | © The Royal Society of Chemistry 2017 | en_US |
dc.rights | 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/). | en_US |
dc.rights | 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 | en_US |
dc.title | Photosensitizer-free visible light-mediated gold-catalysed cis-difunctionalization of silyl-substituted alkynes | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.spage | 7537 | - |
dc.identifier.epage | 7544 | - |
dc.identifier.volume | 8 | - |
dc.identifier.issue | 11 | - |
dc.identifier.doi | 10.1039/c7sc02294h | - |
dcterms.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. | - |
dcterms.accessRights | open access | en_US |
dcterms.bibliographicCitation | Chemical science, 2017, v. 8, no. 11, p. 7537-7544 | - |
dcterms.isPartOf | Chemical science | - |
dcterms.issued | 2017 | - |
dc.identifier.isi | WOS:000413532800029 | - |
dc.identifier.scopus | 2-s2.0-85032013935 | - |
dc.identifier.eissn | 2041-6539 | - |
dc.identifier.rosgroupid | 2017005807 | - |
dc.description.ros | 2017-2018 > Academic research: refereed > Publication in refereed journal | - |
dc.description.validate | 201805 bcrc | - |
dc.description.oa | Version of Record | en_US |
dc.identifier.FolderNumber | OA_IR/PIRA | en_US |
dc.description.pubStatus | Published | en_US |
Appears in Collections: | Journal/Magazine Article |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Deng_Photosensitizer_Free_Visible.pdf | 2.63 MB | Adobe PDF | View/Open |
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