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http://hdl.handle.net/2445/114029
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DC Field | Value | Language |
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dc.contributor.author | Gandioso, Albert | - |
dc.contributor.author | Palau Requena, Marta | - |
dc.contributor.author | Nin-Hill, Alba | - |
dc.contributor.author | Melnyk, Ivanna | - |
dc.contributor.author | Rovira i Virgili, Carme | - |
dc.contributor.author | Nonell, Santi | - |
dc.contributor.author | Velasco Castrillo, Dolores | - |
dc.contributor.author | Garcia Amorós, Jaume | - |
dc.contributor.author | Marchán Sancho, Vicente | - |
dc.date.accessioned | 2017-07-19T08:16:21Z | - |
dc.date.available | 2017-07-19T08:16:21Z | - |
dc.date.issued | 2017-07 | - |
dc.identifier.issn | 2191-1363 | - |
dc.identifier.uri | http://hdl.handle.net/2445/114029 | - |
dc.description.abstract | We report the synthesis and photochemical properties of a series of dicyanocoumarinylmethyl (DEAdcCM)- and dicyanocoumarinylethyl (DEAdcCE)-based photocages of carboxylic acids and amines with absorption maximum around 500 nm. Photolysis studies with green light have demonstrated that the structure of the coumarin chromophore as well as the nature of the leaving group and the type of bond to be photocleaved (ester or carbamate) have a strong influence on the rate and efficiency of the uncaging process. These experimental observations were also supported by DFT calculations. Such differences in deprotection kinetics have been exploited to sequentially photolyze two dicyanocoumarin-caged model compounds (e.g. benzoic acid and ethylamine), and open the way to increasing the number of functional levels that can be addressed with light in a single system, particularly when combining dicyanocoumarin caging groups with other photocleavable protecting groups that remain intact under green light irradiation. | - |
dc.format.extent | 10 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Wiley-VCH Verlag | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1002/open.201700067 | - |
dc.relation.ispartof | ChemistryOpen, 2017, vol. 6, num. 3, p. 375-384 | - |
dc.relation.uri | https://doi.org/10.1002/open.201700067 | - |
dc.rights | cc-by-nc-nd (c) Gandioso, Albert et al., 2017 | - |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/es | - |
dc.source | Articles publicats en revistes (Química Inorgànica i Orgànica) | - |
dc.subject.classification | Llum | - |
dc.subject.classification | Fotoquímica | - |
dc.subject.classification | Síntesi orgànica | - |
dc.subject.classification | Cumarines | - |
dc.subject.other | Light | - |
dc.subject.other | Photochemistry | - |
dc.subject.other | Organic synthesis | - |
dc.subject.other | Coumarins | - |
dc.title | Sequential uncaging with green light can be achieved by fine-tuning the structure of a dicyanocoumarin chromophore | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.identifier.idgrec | 671085 | - |
dc.date.updated | 2017-07-19T08:16:21Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
dc.identifier.pmid | 28638770 | - |
Appears in Collections: | Articles publicats en revistes (Química Inorgànica i Orgànica) |
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671085.pdf | 1.03 MB | Adobe PDF | View/Open |
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