An lcy-topology amino acid MOF as eco-friendly catalyst for cyclic carbonate synthesis from CO2: Structure-DFT corroborated study

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dc.contributor.authorKathalikkattil, Amal Cherianko
dc.contributor.authorBabu, Robinko
dc.contributor.authorRoshan, Roshith Kuruppathparambilko
dc.contributor.authorLee, Hankyulko
dc.contributor.authorKim, Hyungjunko
dc.contributor.authorTharun, Joseko
dc.contributor.authorSuresh, Eringathodiko
dc.contributor.authorPark, Dae-Wonko
dc.date.accessioned2016-05-16T09:00:44Z-
dc.date.available2016-05-16T09:00:44Z-
dc.date.created2015-12-14-
dc.date.created2015-12-14-
dc.date.issued2015-
dc.identifier.citationJOURNAL OF MATERIALS CHEMISTRY A, v.3, no.45, pp.22636 - 22647-
dc.identifier.issn2050-7488-
dc.identifier.urihttp://hdl.handle.net/10203/207560-
dc.description.abstractThe concept of bio-metal-organic framework (bio-MOF) catalysts for CO2 transformation was devised using L-glutamic acid as the natural surrogate for synthetic ligands, and demonstrated their catalytic efficacy for the first time, in the cycloaddition of CO2 with epoxides, supplemented with the structure-DFT correlation. The water stable amino acid bio-MOF, zinc-glutamate-MOF (ZnGlu), with a rare 3D topology (3(3).5(9).6(3))-lcy was synthesized as single crystals and bulk, through an ecofriendly protocol in aqueous medium, from zinc and the proteinogenic amino acid, L-glutamic acid. Amino acid MOFs (AA-MOFs), owing to their economic and environmental factors, are expected to be the future of MOF chemistry at industrial levels. The ZnGlu catalyst with open metal sites was successfully demonstrated as the first bio-MOF catalyst for cyclic carbonate synthesis from CO2 and epoxides, and its efficiency was compared with those of prominent synthetic MOFs reported so far in the process. The as-synthesized catalyst operated even under moist conditions, was thermally and chemically stable; heterogeneous, easily separable (due to its high selectivity, absence of synthesis solvents, and easy catalyst recovery by filtration) and was recycled up to four times. Mechanistic aspects, possible intermediates, transition states and pathways were portrayed using a combination of the experimental inferences, previous reports and ab initio quantum mechanical calculations (DFT techniques) by its correlation with the single crystal XRD structure and topology.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectMETAL-ORGANIC FRAMEWORK-
dc.subjectEFFICIENT HETEROGENEOUS CATALYST-
dc.subjectINTERPENETRATED (3(3).5(9).6(3))-LCY NET-
dc.subjectALLYL GLYCIDYL ETHER-
dc.subjectONE-POT-SYNTHESIS-
dc.subjectSTYRENE CARBONATE-
dc.subjectCHEMICAL FIXATION-
dc.subjectFUNCTIONALIZED IRMOF-3-
dc.subjectCRYSTAL-STRUCTURE-
dc.subjectPROPYLENE-OXIDE-
dc.titleAn lcy-topology amino acid MOF as eco-friendly catalyst for cyclic carbonate synthesis from CO2: Structure-DFT corroborated study-
dc.typeArticle-
dc.identifier.wosid000365011400015-
dc.identifier.scopusid2-s2.0-84946944050-
dc.type.rimsART-
dc.citation.volume3-
dc.citation.issue45-
dc.citation.beginningpage22636-
dc.citation.endingpage22647-
dc.citation.publicationnameJOURNAL OF MATERIALS CHEMISTRY A-
dc.identifier.doi10.1039/c5ta05688h-
dc.contributor.localauthorKim, Hyungjun-
dc.contributor.nonIdAuthorKathalikkattil, Amal Cherian-
dc.contributor.nonIdAuthorBabu, Robin-
dc.contributor.nonIdAuthorRoshan, Roshith Kuruppathparambil-
dc.contributor.nonIdAuthorTharun, Jose-
dc.contributor.nonIdAuthorSuresh, Eringathodi-
dc.contributor.nonIdAuthorPark, Dae-Won-
dc.type.journalArticleArticle-
dc.subject.keywordPlusMETAL-ORGANIC FRAMEWORK-
dc.subject.keywordPlusEFFICIENT HETEROGENEOUS CATALYST-
dc.subject.keywordPlusINTERPENETRATED (3(3).5(9).6(3))-LCY NET-
dc.subject.keywordPlusALLYL GLYCIDYL ETHER-
dc.subject.keywordPlusONE-POT-SYNTHESIS-
dc.subject.keywordPlusSTYRENE CARBONATE-
dc.subject.keywordPlusCHEMICAL FIXATION-
dc.subject.keywordPlusFUNCTIONALIZED IRMOF-3-
dc.subject.keywordPlusCRYSTAL-STRUCTURE-
dc.subject.keywordPlusPROPYLENE-OXIDE-
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EEW-Journal Papers(저널논문)
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