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dc.contributor.authorBertrand, Guillaume
dc.contributor.authorMichaelis, Vladimir K.
dc.contributor.authorOng, Ta-Chung
dc.contributor.authorGriffin, Robert Guy
dc.contributor.authorDinca, Mircea
dc.date.accessioned2013-10-03T17:12:50Z
dc.date.available2013-10-03T17:12:50Z
dc.date.issued2013-03
dc.date.submitted2012-12
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/81293
dc.description.abstractWe report the synthesis and characterization of covalent organic frameworks (COFs) incorporating thiophene-based building blocks. We show that these are amenable to reticular synthesis, and that bent ditopic monomers, such as 2,5-thiophenediboronic acid, are defect-prone building blocks that are susceptible to synthetic variations during COF synthesis. The synthesis and characterization of an unusual charge transfer complex between thieno[3,2-b]thiophene-2,5-diboronic acid and tetracyanoquinodimethane enabled by the unique COF architecture is also presented. Together, these results delineate important synthetic advances toward the implementation of COFs in electronic devices.en_US
dc.description.sponsorshipUnited States. Dept. of Energy. Office of Basic Energy Sciences (Award DE-SC0006937)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB001960)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB002026)en_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1221824110en_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.sourcePNASen_US
dc.titleThiophene-based covalent organic frameworksen_US
dc.typeArticleen_US
dc.identifier.citationBertrand, G. H. V., V. K. Michaelis, T.-C. Ong, R. G. Griffin, and M. Dinca. “Thiophene-based covalent organic frameworks.” Proceedings of the National Academy of Sciences 110, no. 13 (March 26, 2013): 4923-4928.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentFrancis Bitter Magnet Laboratory (Massachusetts Institute of Technology)en_US
dc.contributor.mitauthorBertrand, Guillaumeen_US
dc.contributor.mitauthorMichaelis, Vladimir K.en_US
dc.contributor.mitauthorOng, Ta-Chungen_US
dc.contributor.mitauthorGriffin, Robert Guyen_US
dc.contributor.mitauthorDinca, Mirceaen_US
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsBertrand, G. H. V.; Michaelis, V. K.; Ong, T.-C.; Griffin, R. G.; Dinca, M.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1589-832X
dc.identifier.orcidhttps://orcid.org/0000-0002-1262-1264
dc.identifier.orcidhttps://orcid.org/0000-0002-6708-7660
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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