Lewis acid catalysed polymerisation of cyclopentenone

A modest structural change of a β-diketiminate-supported aluminium complex leads to dramatic differences in the reactivity towards cyclopentenone. While the bulkier complex efficiently executes Diels Alder transformations the smaller analogue performs unique polymerisation of this substrate. This ob...

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Vydané v:Chemical science (Cambridge) Ročník 15; číslo 2; s. 639 - 643
Hlavní autori: Dissanayake, Deepamali, Draper, Alysia, Liu, Zhizhou, Jaunnoo, Neelofur, Haven, Joris J, Forsyth, Craig, McKay, Alasdair I, Junkers, Tanja, Vidovi, Dragoslav
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England Royal Society of Chemistry 03.01.2024
The Royal Society of Chemistry
Predmet:
Chemistry
Lewis acid
Polymerization
Substrates
ISSN:2041-6520, 2041-6539
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Shrnutí:A modest structural change of a β-diketiminate-supported aluminium complex leads to dramatic differences in the reactivity towards cyclopentenone. While the bulkier complex efficiently executes Diels Alder transformations the smaller analogue performs unique polymerisation of this substrate. This observation appears to be unprecedented in the chemistry of Lewis acids and cyclic dienophiles as it represents a unique way to polymerise a functionalised olefin. A modest structural change of a β-diketiminate-supported aluminium complex leads to dramatic differences in the reactivity towards cyclopentenone.
Bibliografia:Electronic supplementary information (ESI) available. CCDC
For ESI and crystallographic data in CIF or other electronic format see DOI
https://doi.org/10.1039/d3sc05186b
2175768-2175770
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SourceType-Scholarly Journals-1
ObjectType-Feature-2
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D. D., A. D. and L. Z. contributed equally to the synthetic part of this work.
ISSN:2041-6520
2041-6539
DOI:10.1039/d3sc05186b