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dc.contributor.authorComito, Robert J
dc.contributor.authorWu, Zhenwei
dc.contributor.authorZhang, Guanghui
dc.contributor.authorLawrence, John A.
dc.contributor.authorKorzynski, Maciej Damian
dc.contributor.authorKehl, Jeffrey A.
dc.contributor.authorMiller, Jeffrey T.
dc.contributor.authorDinca, Mircea
dc.date.accessioned2020-07-13T15:09:05Z
dc.date.available2020-07-13T15:09:05Z
dc.date.issued2018-06
dc.identifier.issn0570-0833
dc.identifier.urihttps://hdl.handle.net/1721.1/126149
dc.description.abstractVanadium catalysts offer unique selectivity in olefin polymerization, yet are underutilized industrially owing to their poor stability and productivity. Reported here is the immobilization of vanadium by cation exchange in MFU-4l, thus providing a metal–organic framework (MOF) with vanadium in a molecule-like coordination environment. This material forms a single-site heterogeneous catalyst with methylaluminoxane and provides polyethylene with low polydispersity (PDI≈3) and the highest activity (up to 148 000 h−1) reported for a MOF-based polymerization catalyst. Furthermore, polyethylene is obtained as a free-flowing powder as desired industrially. Finally, the catalyst shows good structural integrity and retains polymerization activity for over 24 hours, both promising attributes for the commercialization of vanadium-based polyolefins.en_US
dc.description.sponsorshipNational Science Foundation (grant no. DMR-1452612)en_US
dc.language.isoen
dc.publisherWileyen_US
dc.relation.isversionof10.1002/ANIE.201803642en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceMIT web domainen_US
dc.titleStabilized Vanadium Catalyst for Olefin Polymerization by Site Isolation in a Metal-Organic Frameworken_US
dc.typeArticleen_US
dc.identifier.citationComito, Robert J., et al. "Stabilized Vanadium Catalyst for Olefin Polymerization by Site Isolation in a Metal-Organic Framework." Angewandte Chemie International Edition 57, 27 (June 2018): p. 8135-39 doi 10.1002/ANIE.201803642 ©2018 Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalAngewandte Chemie International Editionen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-12-17T14:07:39Z
dspace.date.submission2019-12-17T14:07:41Z
mit.journal.volume57en_US
mit.journal.issue27en_US
mit.metadata.statusComplete


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