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dc.contributor.authorSwager, Timothy M
dc.contributor.authorBatson, Joel Marcus
dc.date.accessioned2019-06-25T16:59:45Z
dc.date.available2019-06-25T16:59:45Z
dc.date.issued2012-08-27
dc.identifier.issn2161-1653
dc.identifier.urihttps://hdl.handle.net/1721.1/121411
dc.description.abstractWe report a versatile new synthetic route to poly(para-phenylene)s (PPPs) and related poly(para-arylene)s containing high degrees of substitution not readily available by other methods. Our method transforms highly soluble, alkyne-containing polymers into PPPs via high-yielding, transition metal-mediated [2+2+2] cyclizations.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant DMR-1005810)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/mz300352men_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceProf. Swager via Erja Kajosaloen_US
dc.titlePoly(para-arylene)s via [2+2+2]en_US
dc.typeArticleen_US
dc.identifier.citationBatson, Joel M., and Timothy M. Swager. “Poly( Para-Arylene)s via [2+2+2].” ACS Macro Letters, 1, 9 (September 2012): 1121–23.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverSwager, Timothy M.en_US
dc.relation.journalACS Macro Lettersen_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
dspace.embargo.termsNen_US
dspace.date.submission2019-04-04T10:06:20Z
mit.licensePUBLISHER_POLICYen_US


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