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dc.contributor.authorHsia, Liang-Yuen_US
dc.contributor.authorChen, Hsin-Nien_US
dc.contributor.authorChiang, Chun-Haoen_US
dc.contributor.authorHung, Ming-Yangen_US
dc.contributor.authorWei, Hao-Kengen_US
dc.contributor.authorLuo, Chih-Weien_US
dc.contributor.authorKuo, Ming-Yuen_US
dc.contributor.authorLuo, Shun-Yuanen_US
dc.contributor.authorChu, Chih-Chienen_US
dc.date.accessioned2020-10-05T02:01:07Z-
dc.date.available2020-10-05T02:01:07Z-
dc.date.issued2020-07-17en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.joc.0c00901en_US
dc.identifier.urihttp://hdl.handle.net/11536/155161-
dc.description.abstractNovel coumarin-iminophosphorane (IPP) fluorophores that have stable resonance contributions from aza-ylides were formed by using the nonhydrolysis Staudinger reaction. The N=P formation reaction kinetics obey the conventional Staudinger reaction. The absorption and emission profiles of the coumarin-IPP derivatives can be fine-tuned: an electron-donating group at PPh3 enhances absorption and fluorescence, whereas an electron-withdrawing group at C-3 drives absorption and emission peaks toward blue-light wavelengths. Two-photon adsorption, accompanied by anti-Stokes fluorescence, is achieved under near-infrared femtosecond laser excitation.en_US
dc.language.isoen_USen_US
dc.titlepi-Extended Coumarins Derived with Nonhydrolyzable Iminophosphoranes as Two-Photon-Excited Fluorophoresen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.joc.0c00901en_US
dc.identifier.journalJOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volume85en_US
dc.citation.issue14en_US
dc.citation.spage9361en_US
dc.citation.epage9366en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000551550500055en_US
dc.citation.woscount0en_US
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