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dc.contributor.author | Ramírez Palma, María Teresa | |
dc.contributor.author | Apolonio, Víctor M. | |
dc.contributor.author | González, Jaime | |
dc.contributor.author | Martínez Barrera, Gonzalo | |
dc.contributor.author | Corona-Becerril, David | |
dc.contributor.author | Cuevas-Yañez, Erick | |
dc.date.accessioned | 2018-03-13T05:30:42Z | |
dc.date.available | 2018-03-13T05:30:42Z | |
dc.date.issued | 2017-12-01 | |
dc.identifier.issn | 1060-1325 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11799/79885 | |
dc.description | Artículo para obtención de grado de Doctor | es |
dc.description.abstract | A novel class of thermostable G0 and G1-dendrimers was synthesized from the coupling of both propargyl and azido esters derived from EDTA through copper catalyzed azide-alkyne cycloaddition. The branching and size in these compounds were controlled by a simple azide-alkyne group position change in the CuAAC reaction in conjunction with the use of 1,3-diazido-propan-2-ol as a polyfunctional compound. | es |
dc.language.iso | eng | es |
dc.publisher | Taylor and Francis | es |
dc.rights | embargoedAccess | es |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/4.0/ | es |
dc.rights | embargoedAccess | es |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/4.0/ | es |
dc.subject | Dendrimers | es |
dc.subject | EDTA | es |
dc.subject | synthesis | es |
dc.subject | esterification | es |
dc.title | Synthesis of EDTA core dendrimers through a consecutive esterification-CuAAC process | es |
dc.type | Artículo | es |
dc.provenance | Científica | es |
dc.road | Dorada | es |
dc.organismo | Química | es |
dc.ambito | Internacional | es |
dc.cve.CenCos | 20401 | es |
dc.cve.progEstudios | 724 | es |