dc.contributor.author | Uriel, Clara | |
dc.contributor.author | Gómez López, Ana María | |
dc.contributor.author | García Martínez de la Hidalga, Enrique | |
dc.contributor.author | Bañuelos Prieto, Jorge | |
dc.contributor.author | García Moreno, Inmaculada | |
dc.contributor.author | López Pérez, José Cristóbal | |
dc.date.accessioned | 2021-10-11T09:30:27Z | |
dc.date.available | 2021-10-11T09:30:27Z | |
dc.date.issued | 2021-09-03 | |
dc.identifier.citation | Organic Letters 23(17) : 6801-6806 (2021) | es_ES |
dc.identifier.issn | 1523-7060 | |
dc.identifier.issn | 1523-7052 | |
dc.identifier.uri | http://hdl.handle.net/10810/53343 | |
dc.description.abstract | Hitherto unreported 2,6-dipropargyl-1,3,5,7-tetramethyl BODIPYs can be efficiently prepared by a Nicholas reaction/decomplexation protocol from 1,3,5,7-tetramethyl BODIPYs. The title compounds, which improve the BODIPY photostability by retaining their inherent photophysical and photochemical properties, can be engaged in efficient copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) "click-type" reactions with azido derivatives to provide all-BODIPY-triads or conjugated BODIPYs. | es_ES |
dc.description.sponsorship | We gratefully acknowledge the Spanish Ministerio de Ciencia e Innovacion for financial support (Project Nos. RTI2018094862-B-100, MAT2017-83856-C3-1-P and 3-P; PiD2020114755GB-C31 and -C33) and the Gobierno Vasco (GV) (Project No. IT912-16) for financial support. We are indebted to Ms. Marina Rodriguez (IQOG-CSIC) for skillful technical support. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | American Chemical Society | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/RTI2018-094862-B-100 | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/MAT2017-83856-C3-1-P | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/MAT2017-83856-C3-3-P | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/PiD2020-114755GB-C31 | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/PiD2020-114755GB-C33 | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.subject | derivatives | es_ES |
dc.subject | chemistry | es_ES |
dc.subject | probes | es_ES |
dc.title | Access to 2,6-Dipropargylated BODIPYs as "Clickable" Congeners of Pyrromethene-567 Dye: Photostability and Synthetic Versatility | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.holder | This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) | es_ES |
dc.rights.holder | Atribución 3.0 España | * |
dc.relation.publisherversion | https://pubs-acs-org.ehu.idm.oclc.org/doi/10.1021/acs.orglett.1c02380 | es_ES |
dc.identifier.doi | 10.1021/acs.orglett.1c02380 | |
dc.departamentoes | Química física | es_ES |
dc.departamentoeu | Kimika fisikoa | es_ES |