2021
DOI: 10.1039/d0cy01863e
|View full text |Cite
|
Sign up to set email alerts
|

Selective dimerisation of 1-hexene mediated by aluminium alkyl chloride-activated tungsten imido complexes

Abstract: The selective dimerisation of 1-hexene to dodecenes was accomplished using catalysts generated from a tungsten mono- [WCl4(NR)(thf)] or bis- [WCl2(NR)2(dme)] imido complex following activation with EtAlCl2. These catalytic systems achieve...

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 36 publications
0
1
0
Order By: Relevance
“…13, which can dimerize 1-hexene with activities comparable to other non-metallocenebased complexes studied earlier for such alpha olefin oligomerizations. 69 In contrast, when analogous Nb and Ta imido complexes were synthesized and tested for 1-hexene dimeriza- tion, almost all the catalysts showed very poor activity with <5% olefin conversion and total C 6 oligomer (C 12 + C 18 ) fraction yielding a mere 2%. The pronounced propensity for the isomerization of linear olefins to internal olefins (∼40% isomers) is mainly attributed to the Lewis acidic nature of the EtAlCl 2 activator employed in these reactions.…”
Section: Polymer Chemistry Reviewmentioning
confidence: 99%
“…13, which can dimerize 1-hexene with activities comparable to other non-metallocenebased complexes studied earlier for such alpha olefin oligomerizations. 69 In contrast, when analogous Nb and Ta imido complexes were synthesized and tested for 1-hexene dimeriza- tion, almost all the catalysts showed very poor activity with <5% olefin conversion and total C 6 oligomer (C 12 + C 18 ) fraction yielding a mere 2%. The pronounced propensity for the isomerization of linear olefins to internal olefins (∼40% isomers) is mainly attributed to the Lewis acidic nature of the EtAlCl 2 activator employed in these reactions.…”
Section: Polymer Chemistry Reviewmentioning
confidence: 99%