000070911 001__ 70911
000070911 005__ 20191122145055.0
000070911 0247_ $$2doi$$a10.1186/s13065-018-0393-6
000070911 0248_ $$2sideral$$a106371
000070911 037__ $$aART-2018-106371
000070911 041__ $$aeng
000070911 100__ $$aSalah, A.M.B.
000070911 245__ $$aSynthesis, structural determination and antimicrobial evaluation of two novel CoII and ZnII halogenometallates as efficient catalysts for the acetalization reaction of aldehydes
000070911 260__ $$c2018
000070911 5060_ $$aAccess copy available to the general public$$fUnrestricted
000070911 5203_ $$aBackground: Complexes of imidazole derivatives with transition metal ions have attracted much attention because of their biological and pharmacological activities, such as antimicrobial, antifungal, antiallergic, antitumoural and antimetastatic properties. In addition, imidazoles occupy an important place owing to their meaningful catalytic activity in several processes, such as in hydroamination, hydrosilylation, Heck reaction and Henry reaction. In this work, we describe the crystallization of two halogenometallate based on 2-methylimidazole. Their IR, thermal analysis, catalytic properties and antibacterial activities have also been investigated. Results: Two new isostructural organic-inorganic hybrid materials, based on 2-methyl-1H-imidazole, 1 and 2, were synthesized and fully structurally characterized. The analysis of their crystal packing reveals non-covalent interactions, including C/N–HCl hydrogen bonds and stacking interactions, to be the main factor governing the supramolecular assembly of the crystalline complexes. The thermal decomposition of the complexes is a mono-stage process, confirmed by the three-dimensional representation of the powder diffraction patterns (TDXD). The catalytic structure exhibited promising activity using MeOH as solvent and as the unique source of acetalization. Moreover, the antimicrobial results suggested that metal-complexes exhibit significant antimicrobial activity. Conclusion: This study highlights again the structural and the biological diversities within the field of inorganic–organic hybrids. [Figure not available: see fulltext.].
000070911 536__ $$9info:eu-repo/grantAgreement/ES/MINECO/CTQ2017-88091-P
000070911 540__ $$9info:eu-repo/semantics/openAccess$$aby$$uhttp://creativecommons.org/licenses/by/3.0/es/
000070911 590__ $$a2.094$$b2018
000070911 591__ $$aCHEMISTRY, MULTIDISCIPLINARY$$b92 / 172 = 0.535$$c2018$$dQ3$$eT2
000070911 592__ $$a0.489$$b2018
000070911 593__ $$aChemistry (miscellaneous)$$c2018$$dQ2
000070911 655_4 $$ainfo:eu-repo/semantics/article$$vinfo:eu-repo/semantics/publishedVersion
000070911 700__ $$aFendri, L.B.
000070911 700__ $$aBataille, T.
000070911 700__ $$0(orcid)0000-0002-5244-9569$$aPérez Herrera, R.$$uUniversidad de Zaragoza
000070911 700__ $$aNaïli, H.
000070911 7102_ $$12013$$2765$$aUniversidad de Zaragoza$$bDpto. Química Orgánica$$cÁrea Química Orgánica
000070911 773__ $$g12, 1 (2018), 24 [12 pp]$$pChemistry Central Journal$$tChemistry Central Journal$$x1752-153X
000070911 8564_ $$s1696152$$uhttp://zaguan.unizar.es/record/70911/files/texto_completo.pdf$$yVersión publicada
000070911 8564_ $$s76542$$uhttp://zaguan.unizar.es/record/70911/files/texto_completo.jpg?subformat=icon$$xicon$$yVersión publicada
000070911 909CO $$ooai:zaguan.unizar.es:70911$$particulos$$pdriver
000070911 951__ $$a2019-11-22-14:44:57
000070911 980__ $$aARTICLE