Reactivity studies of phosphorus-stabilised yttrium carbene complexes
Reactivity studies of [Y(BIPM)(I)(THF)2] (73), [Y(BIPM)(CH2SiMe3)(THF)] (74) and [Y(BIPM)(CH2Ph)(THF)] (75) towards a range of unsaturated compounds have been performed. The isolation of single crystals suitable for X-ray diffraction studies for all the systems investigated has proven problematic. T...
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ndltd-bl.uk-oai-ethos.bl.uk-7542142019-02-05T03:33:26ZReactivity studies of phosphorus-stabilised yttrium carbene complexesSoutar, Lyndsay2016Reactivity studies of [Y(BIPM)(I)(THF)2] (73), [Y(BIPM)(CH2SiMe3)(THF)] (74) and [Y(BIPM)(CH2Ph)(THF)] (75) towards a range of unsaturated compounds have been performed. The isolation of single crystals suitable for X-ray diffraction studies for all the systems investigated has proven problematic. The low crystalline yields observed, where crystals of suitable quality for single crystal X-ray diffraction studies were obtainable, is a reflection of the high solubility of many of the products. The reactivity of 74 and 75 towards anthracene aldehyde and benzaldehyde revealed Wittig-type reactivity to yield the alkene products (Me3SiNPPh2)2C=C(H)R (65) (R = 9-anthracene) and (Me3SiNPPh2)2C=C(H)Ph (66), respectively. The respective reactions of 74 and 75 with four equivalents of acetophenone yielded the previously reported dypnopinacol 111 via a cyclotetramerization reaction.540University of Nottinghamhttps://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.754214Electronic Thesis or Dissertation |
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540 Soutar, Lyndsay Reactivity studies of phosphorus-stabilised yttrium carbene complexes |
description |
Reactivity studies of [Y(BIPM)(I)(THF)2] (73), [Y(BIPM)(CH2SiMe3)(THF)] (74) and [Y(BIPM)(CH2Ph)(THF)] (75) towards a range of unsaturated compounds have been performed. The isolation of single crystals suitable for X-ray diffraction studies for all the systems investigated has proven problematic. The low crystalline yields observed, where crystals of suitable quality for single crystal X-ray diffraction studies were obtainable, is a reflection of the high solubility of many of the products. The reactivity of 74 and 75 towards anthracene aldehyde and benzaldehyde revealed Wittig-type reactivity to yield the alkene products (Me3SiNPPh2)2C=C(H)R (65) (R = 9-anthracene) and (Me3SiNPPh2)2C=C(H)Ph (66), respectively. The respective reactions of 74 and 75 with four equivalents of acetophenone yielded the previously reported dypnopinacol 111 via a cyclotetramerization reaction. |
author |
Soutar, Lyndsay |
author_facet |
Soutar, Lyndsay |
author_sort |
Soutar, Lyndsay |
title |
Reactivity studies of phosphorus-stabilised yttrium carbene complexes |
title_short |
Reactivity studies of phosphorus-stabilised yttrium carbene complexes |
title_full |
Reactivity studies of phosphorus-stabilised yttrium carbene complexes |
title_fullStr |
Reactivity studies of phosphorus-stabilised yttrium carbene complexes |
title_full_unstemmed |
Reactivity studies of phosphorus-stabilised yttrium carbene complexes |
title_sort |
reactivity studies of phosphorus-stabilised yttrium carbene complexes |
publisher |
University of Nottingham |
publishDate |
2016 |
url |
https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.754214 |
work_keys_str_mv |
AT soutarlyndsay reactivitystudiesofphosphorusstabilisedyttriumcarbenecomplexes |
_version_ |
1718973735221854208 |