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Polymers and oligomers with transverse aromatic groups and tightly controlled chain conformations

dc.contributor.authorAlder, R. W.en
dc.contributor.authorAnderson, K. R.en
dc.contributor.authorBenjes, P. A.en
dc.contributor.authorButts, C. P.en
dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.contributor.authorGuy Orpen, A.en
dc.creatorAlder, R. W.en
dc.creatorAnderson, K. R.en
dc.creatorBenjes, P. A.en
dc.creatorButts, C. P.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.creatorGuy Orpen, A.en
dc.date.accessioned2019-11-21T06:16:18Z
dc.date.available2019-11-21T06:16:18Z
dc.date.issued1998
dc.identifier.issn1359-7345
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55243
dc.description.abstractAnionic ring-opening polymerisation of spiro[cyclopropane-1,9′-fluorene] with fluorenyl anion as initiator yields polymers 1 with chains which are essentially all-anti and have transversely-oriented fluorenyl groups, as shown by strong upfield shifts for the mid-chain methylene and 1,8-fluorenyl protonsen
dc.description.abstractsynthetic routes to some specific oligomers are also reported.en
dc.sourceChemical Communicationsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0000249441&partnerID=40&md5=7a71fbf869c61874f05525ed9cb47816
dc.titlePolymers and oligomers with transverse aromatic groups and tightly controlled chain conformationsen
dc.typeinfo:eu-repo/semantics/article
dc.description.issue3
dc.description.startingpage309
dc.description.endingpage310
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :27</p>en
dc.source.abbreviationChem.Commun.en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.gnosis.orcid0000-0002-4652-7567


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