dc.contributor.author | Swager, Timothy M | |
dc.contributor.author | Batson, Joel Marcus | |
dc.date.accessioned | 2019-06-25T16:59:45Z | |
dc.date.available | 2019-06-25T16:59:45Z | |
dc.date.issued | 2012-08-27 | |
dc.identifier.issn | 2161-1653 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/121411 | |
dc.description.abstract | We 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.sponsorship | National Science Foundation (U.S.) (Grant DMR-1005810) | en_US |
dc.language.iso | en_US | |
dc.publisher | American Chemical Society | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/mz300352m | en_US |
dc.rights | Article 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.source | Prof. Swager via Erja Kajosalo | en_US |
dc.title | Poly(para-arylene)s via [2+2+2] | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Batson, 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.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
dc.contributor.approver | Swager, Timothy M. | en_US |
dc.relation.journal | ACS Macro Letters | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.embargo.terms | N | en_US |
dspace.date.submission | 2019-04-04T10:06:20Z | |
mit.license | PUBLISHER_POLICY | en_US |