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dc.contributor.authorDane, Eric L.
dc.contributor.authorSwager, Timothy Manning
dc.date.accessioned2011-12-15T18:23:26Z
dc.date.available2011-12-15T18:23:26Z
dc.date.issued2010-09
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.urihttp://hdl.handle.net/1721.1/67695
dc.descriptionExperimental details and additional spectra are available free of charge via the Internet at http://pubs.acs.org.en_US
dc.description.abstractThe synthesis of poly-1,3-bisdiphenylene-2-phenyl allyl (BDPA) radicals via a new anionic oligomerization strategy is reported. The material displays a reversible reduction from the orange-red radical to the blue carbanion in solution.en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol1017728en_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. Swageren_US
dc.titleCarbanionic Route to Electroactive Carbon-Centered Anion and Radical Oligomersen_US
dc.typeArticleen_US
dc.identifier.citationDane, Eric L., and Timothy M. Swager. “Carbanionic Route to Electroactive Carbon-Centered Anion and Radical Oligomers.” Organic Letters 12 (2010): 4324-4327. Web. 15 Dec. 2011. © 2011 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverSwager, Timothy Manning
dc.contributor.mitauthorDane, Eric L.
dc.contributor.mitauthorSwager, Timothy M.
dc.relation.journalOrganic 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.orderedauthorsDane, Eric L.; Swager, Timothy M.en
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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