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dc.contributor.authorTan, N.
dc.contributor.authorSimpson, Peter
dc.contributor.authorNealon, G.
dc.contributor.authorSobolev, A.
dc.contributor.authorRaiteri, Paolo
dc.contributor.authorMassi, Massimiliano
dc.contributor.authorOgden, Mark
dc.contributor.authorLowe, Andrew
dc.date.accessioned2019-02-19T04:17:55Z
dc.date.available2019-02-19T04:17:55Z
dc.date.created2019-02-19T03:58:18Z
dc.date.issued2019
dc.identifier.citationTan, N. and Simpson, P. and Nealon, G. and Sobolev, A. and Raiteri, P. and Massi, M. and Ogden, M. et al. 2019. Rhodium(I)-a-Phenylvinylfluorenyl Complexes: Synthesis, Characterization, and Evaluation as Initiators in the Stereospecific Polymerization of Phenylacetylene. European Journal of Inorganic Chemistry. 2019 (5): pp. 592-601.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/74718
dc.identifier.doi10.1002/ejic.201801411
dc.description.abstract

The synthesis, characterization and use, as initiators for phenylacetylene polymerizations, of three new rhodium(I)-vinyl complexes containing fluorenyl functionality with fluorine-functionalized phosphine ligands is described. Rh(nbd)(CPh=CFlu)P(4-FC6H4)3, Rh(nbd)(CPh=CFlu)P(4-CF3C6H4)3, and Rh(nbd)(CPh=CFlu)P[3,5-(CF3)2C6H3]3 (nbd: 2,5-norbornadiene; Flu: fluorenyl) were prepared and isolated as discrete, orange compounds and were readily recrystallized yielding X-ray quality crystals. All complexes were characterized by a combination of 1H, 31P, 19F, 103Rh NMR spectroscopy and 2D 31P-103Rh/31P-103Rh{103Rh} heteronuclear multiple-quantum correlation (HMQC) experiments, elemental analysis, and single-crystal X-ray analysis. The complexes were active as initiators in the co-ordination insertion polymerization of phenylacetylene, with initiation efficiencies spanning the range 13–56 %, and yielded polyphenylacetylenes of low dispersity (Ð = Mw/Mn) with high cis-transoidal stereoregularity.

dc.publisherWiley - V C H Verlag GmbH
dc.titleRhodium(I)-a-Phenylvinylfluorenyl Complexes: Synthesis, Characterization, and Evaluation as Initiators in the Stereospecific Polymerization of Phenylacetylene
dc.typeJournal Article
dcterms.source.volume2019
dcterms.source.number5
dcterms.source.startPage592
dcterms.source.endPage601
dcterms.source.issn1434-1948
dcterms.source.titleEuropean Journal of Inorganic Chemistry
curtin.departmentNanochemistry Research Institute
curtin.accessStatusFulltext not available


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