Substituted indenyl complexes for ethylene polymerisation

<p>The principle aims of this thesis have been to synthesise novel substituted indenyl complexes inspired by the very active <sup>Me<sub>2</sub></sup>SBI*ZrCl<sub>2</sub>. By looking to improve on the ethylene polymerisation activity and the racemo-selectivi...

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Main Author: Angpanitcharoen, P
Other Authors: O'Hare, D
Format: Thesis
Language:English
Published: 2018
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author Angpanitcharoen, P
author2 O'Hare, D
author_facet O'Hare, D
Angpanitcharoen, P
author_sort Angpanitcharoen, P
collection OXFORD
description <p>The principle aims of this thesis have been to synthesise novel substituted indenyl complexes inspired by the very active <sup>Me<sub>2</sub></sup>SBI*ZrCl<sub>2</sub>. By looking to improve on the ethylene polymerisation activity and the racemo-selectivity, the <sup>Me<sub>2</sub></sup>SBI* ligand framework has been modified. The synthesised complexes have been tested for homogeneous and heterogeneous ethylene polymerisation activity and evaluated for their potential industrial applications.</p> <p><b>Chapter One</b> provides a background to the chemistry of cyclopentadienyl and indenyl ligands, group 4 ansa-metallocenes and their ethylene polymerisation activity. The mechanism of ethylene polymerisation is reviewed. A summary of the development of homogeneous and heterogeneous ethylene polymerisation is discussed including the use of solid supports; silica, solid polymethylaluminoxane (sMAO) and layered double hydroxides.</p> <p><b>Chapter Two</b> describes modification of the <sup>Me<sub>2</sub></sup>SBI* ligand by introducing different alkyl and aryl groups on the silyl bridge and at the 3position of the indenyl rings. <sup>Et<sub>2</sub></sup>SBI*H<sub>2</sub>, <sup><em>n</em>Pr,Me</sup>SBI*H<sub>2</sub>, All,MeSBI*H2 and <sup>Me<sub>2</sub></sup>SB(3EtI*)H<sub>2</sub> pro-ligands have been synthesised. All pro-ligands and their synthetic intermediates have been fully characterised by NMR spectroscopy.</p> <p><b>Chapter Three</b> details the synthesis of substituted indenyl group 4 complexes. All complexes have been fully characterised by single crystal X-ray diffraction and NMR spectroscopy. Comparisons of the crystal structure metrical parameters are made.</p> <p><b>Chapter Four</b> investigates the homogeneous and heterogeneous ethylene polymerisation activity of the synthesised substituted indenyl complexes. The complexes have been immobilised onto sMAO and characterised by solid state NMR spectroscopy and SEM. The resulting polyethylenes have been characterised by GPC, XRD and SEM.</p> <p><b>Chapter Five</b> studies the solid support comparison between sMAO, SSMAO and LDHMAO. The optimisation of polymerisation conditions for the sMAO-[<sup>Me<sub>2</sub></sup>SB(<sup>3-Et</sup>I*)ZrCl<sub>2</sub>] catalyst has been carried out. Potential industrial applications including polyethylene waxes and LLDPE have been explored.</p> <p><b>Chapter Six</b> provides experimental details and characterising data for the preceding chapters. <b>Electronic appendix</b> contains the CIF, CheckCIF and PLATON files of all single crystal structures.</p>
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spelling oxford-uuid:a5eff05b-b3be-40ff-bc61-25e1735842082022-03-27T02:43:54ZSubstituted indenyl complexes for ethylene polymerisationThesishttp://purl.org/coar/resource_type/c_db06uuid:a5eff05b-b3be-40ff-bc61-25e173584208EnglishORA Deposit2018Angpanitcharoen, PO'Hare, D<p>The principle aims of this thesis have been to synthesise novel substituted indenyl complexes inspired by the very active <sup>Me<sub>2</sub></sup>SBI*ZrCl<sub>2</sub>. By looking to improve on the ethylene polymerisation activity and the racemo-selectivity, the <sup>Me<sub>2</sub></sup>SBI* ligand framework has been modified. The synthesised complexes have been tested for homogeneous and heterogeneous ethylene polymerisation activity and evaluated for their potential industrial applications.</p> <p><b>Chapter One</b> provides a background to the chemistry of cyclopentadienyl and indenyl ligands, group 4 ansa-metallocenes and their ethylene polymerisation activity. The mechanism of ethylene polymerisation is reviewed. A summary of the development of homogeneous and heterogeneous ethylene polymerisation is discussed including the use of solid supports; silica, solid polymethylaluminoxane (sMAO) and layered double hydroxides.</p> <p><b>Chapter Two</b> describes modification of the <sup>Me<sub>2</sub></sup>SBI* ligand by introducing different alkyl and aryl groups on the silyl bridge and at the 3position of the indenyl rings. <sup>Et<sub>2</sub></sup>SBI*H<sub>2</sub>, <sup><em>n</em>Pr,Me</sup>SBI*H<sub>2</sub>, All,MeSBI*H2 and <sup>Me<sub>2</sub></sup>SB(3EtI*)H<sub>2</sub> pro-ligands have been synthesised. All pro-ligands and their synthetic intermediates have been fully characterised by NMR spectroscopy.</p> <p><b>Chapter Three</b> details the synthesis of substituted indenyl group 4 complexes. All complexes have been fully characterised by single crystal X-ray diffraction and NMR spectroscopy. Comparisons of the crystal structure metrical parameters are made.</p> <p><b>Chapter Four</b> investigates the homogeneous and heterogeneous ethylene polymerisation activity of the synthesised substituted indenyl complexes. The complexes have been immobilised onto sMAO and characterised by solid state NMR spectroscopy and SEM. The resulting polyethylenes have been characterised by GPC, XRD and SEM.</p> <p><b>Chapter Five</b> studies the solid support comparison between sMAO, SSMAO and LDHMAO. The optimisation of polymerisation conditions for the sMAO-[<sup>Me<sub>2</sub></sup>SB(<sup>3-Et</sup>I*)ZrCl<sub>2</sub>] catalyst has been carried out. Potential industrial applications including polyethylene waxes and LLDPE have been explored.</p> <p><b>Chapter Six</b> provides experimental details and characterising data for the preceding chapters. <b>Electronic appendix</b> contains the CIF, CheckCIF and PLATON files of all single crystal structures.</p>
spellingShingle Angpanitcharoen, P
Substituted indenyl complexes for ethylene polymerisation
title Substituted indenyl complexes for ethylene polymerisation
title_full Substituted indenyl complexes for ethylene polymerisation
title_fullStr Substituted indenyl complexes for ethylene polymerisation
title_full_unstemmed Substituted indenyl complexes for ethylene polymerisation
title_short Substituted indenyl complexes for ethylene polymerisation
title_sort substituted indenyl complexes for ethylene polymerisation
work_keys_str_mv AT angpanitcharoenp substitutedindenylcomplexesforethylenepolymerisation