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Cu(II)-Schiff base covalently anchored to MIL-125(Ti)-NH2 as heterogeneous catalyst for oxidation reactions

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Cu(II)-Schiff base covalently anchored to MIL-125(Ti)-NH2 as heterogeneous catalyst for oxidation reactions

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Daliran, S.; Santiago-Portillo, A.; Navalón Oltra, S.; Reza Oveisi, A.; Alvaro Rodríguez, MM.; Ghorbani-Vaghei, R.; Azarifar, D.... (2018). Cu(II)-Schiff base covalently anchored to MIL-125(Ti)-NH2 as heterogeneous catalyst for oxidation reactions. Journal of Colloid and Interface Science. 532:700-710. https://doi.org/10.1016/j.jcis.2018.07.140

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/142045

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Title: Cu(II)-Schiff base covalently anchored to MIL-125(Ti)-NH2 as heterogeneous catalyst for oxidation reactions
Author: Daliran, Saba Santiago-Portillo, Andrea Navalón Oltra, Sergio Reza Oveisi, Ali Alvaro Rodríguez, Maria Mercedes Ghorbani-Vaghei, Ramin Azarifar, Davood García Gómez, Hermenegildo
UPV Unit: Universitat Politècnica de València. Departamento de Química - Departament de Química
Issued date:
Abstract:
[EN] MIL-125(Ti)-NH2 has been modified by reaction of salicylaldehyde with the terephthalate amino groups to form a salicylideneimine that act as ligand of Cu2+. The success of the postsynthetic modification was assessed ...[+]
Subjects: Heterogeneous catalysis , Metal-organic frameworks: Cu(II) Schiff-base complex , Terr-butylhydroperoxyde
Copyrigths: Reconocimiento - No comercial - Sin obra derivada (by-nc-nd)
Source:
Journal of Colloid and Interface Science. (issn: 0021-9797 )
DOI: 10.1016/j.jcis.2018.07.140
Publisher:
Elsevier
Publisher version: https://doi.org/10.1016/j.jcis.2018.07.140
Project ID:
GV/PROMETEO/2017/063
Fundació Bancària Caixa d'Estalvis i Pensions de Barcelona/LCF/TR/CI16/10010016
MINECO/CTQ2014-53292-R-AR
Thanks:
Financial support by the Spanish Ministry of Economy and Competitiveness (Severo Ochoa) CTQ2014-53292-R is gratefully acknowledged. Generalidad Valenciana is also thanked for funding (Prometeo 2017/063). S.D., A.R.O., D.A., ...[+]
Type: Artículo

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