Polymerisation of 1,5-hexadienes
Thesis (MSc)--Stellenbosch University, 2001. === ENGLISH ABSTRACT: In this study, the feasibility of the non-conjugated 1,5-hexadiene as monomer in metallocene catalised cyclopolymerizations was considered. Homopolymers and copolymers with ethylene, propylene, 1-pentene, 1-hexene and 2-methyl-1,5...
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ndltd-netd.ac.za-oai-union.ndltd.org-sun-oai-scholar.sun.ac.za-10019.1-524032016-01-29T04:02:46Z Polymerisation of 1,5-hexadienes Smit, Madri Van Reenen, A. J. Stellenbosch University. Faculty of Science. Dept. of Chemistry & Polymer Science. Polymerization Dissertations -- Polymer science Theses -- Polymer science Thesis (MSc)--Stellenbosch University, 2001. ENGLISH ABSTRACT: In this study, the feasibility of the non-conjugated 1,5-hexadiene as monomer in metallocene catalised cyclopolymerizations was considered. Homopolymers and copolymers with ethylene, propylene, 1-pentene, 1-hexene and 2-methyl-1,5- hexadiene as comonomers were synthesised in the presence of Cp2ZrCh and rac-Et(lnd)2Zrh. The microstructure (stereoregularity and cyclisation) and number-average molecular weight were determined from NMR analysis. Crystalline oligomers with functional (eg -OH) and vinylidene end groups were obtained. AFRIKAANSE OPSOMMING: Die studie behels die ondersoek rakende die gebruik van ongekonjugeerde 1,5- heksadieen as monomeer in metalloseengekataliseerde polimerisasies. Homopolimere, sowel as kopolimere van etlieen, propileen, 1-penteen, 1- hekseen en 2-metiel-1,5-heksadieen, is in die teenwoordigheid van Cp2ZrChen rac-Et(lnd)2ZrCI2 gepolimeriseer. Die mikrostruktuur (stereochemie en siklisering) en die getal-gemiddelde molekulêre gewig van die gesintetiseerde polimere is met behulp van KMR spektroskopie ondersoek. Die studie het getoon dat kristallyne oligomere met funksionele (bv -OH) en vinilideen endgroepe gesintetiseer is. 2012-08-27T11:34:59Z 2012-08-27T11:34:59Z 2001-12 Thesis http://hdl.handle.net/10019.1/52403 en_ZA Stellenbosch University 72, [22] p. : ill. Stellenbosch : Stellenbosch University |
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Polymerization Dissertations -- Polymer science Theses -- Polymer science |
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Polymerization Dissertations -- Polymer science Theses -- Polymer science Smit, Madri Polymerisation of 1,5-hexadienes |
description |
Thesis (MSc)--Stellenbosch University, 2001. === ENGLISH ABSTRACT: In this study, the feasibility of the non-conjugated 1,5-hexadiene as monomer in
metallocene catalised cyclopolymerizations was considered. Homopolymers and
copolymers with ethylene, propylene, 1-pentene, 1-hexene and 2-methyl-1,5-
hexadiene as comonomers were synthesised in the presence of Cp2ZrCh and
rac-Et(lnd)2Zrh. The microstructure (stereoregularity and cyclisation) and
number-average molecular weight were determined from NMR analysis.
Crystalline oligomers with functional (eg -OH) and vinylidene end groups were
obtained. === AFRIKAANSE OPSOMMING: Die studie behels die ondersoek rakende die gebruik van ongekonjugeerde 1,5-
heksadieen as monomeer in metalloseengekataliseerde polimerisasies.
Homopolimere, sowel as kopolimere van etlieen, propileen, 1-penteen, 1-
hekseen en 2-metiel-1,5-heksadieen, is in die teenwoordigheid van Cp2ZrChen
rac-Et(lnd)2ZrCI2 gepolimeriseer. Die mikrostruktuur (stereochemie en
siklisering) en die getal-gemiddelde molekulêre gewig van die gesintetiseerde
polimere is met behulp van KMR spektroskopie ondersoek. Die studie het
getoon dat kristallyne oligomere met funksionele (bv -OH) en vinilideen endgroepe
gesintetiseer is. |
author2 |
Van Reenen, A. J. |
author_facet |
Van Reenen, A. J. Smit, Madri |
author |
Smit, Madri |
author_sort |
Smit, Madri |
title |
Polymerisation of 1,5-hexadienes |
title_short |
Polymerisation of 1,5-hexadienes |
title_full |
Polymerisation of 1,5-hexadienes |
title_fullStr |
Polymerisation of 1,5-hexadienes |
title_full_unstemmed |
Polymerisation of 1,5-hexadienes |
title_sort |
polymerisation of 1,5-hexadienes |
publisher |
Stellenbosch : Stellenbosch University |
publishDate |
2012 |
url |
http://hdl.handle.net/10019.1/52403 |
work_keys_str_mv |
AT smitmadri polymerisationof15hexadienes |
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1718163658607951872 |