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Liquid coordination complexes: a new class of Lewis acids as safer alternatives to BF sub(3) in synthesis of polyalphaolefins

Liquid coordination complexes (LCCs) are a new class of liquid Lewis acids, prepared by combining an excess of a metal halide (e.g. GaCl sub(3)) with a basic donor molecule (e.g. amides, amines or phosphines). LCCs were used to catalyse oligomerisation of 1-decene to polyalphaolefins (PAOs). Molecul...

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Published in:Green chemistry : an international journal and green chemistry resource : GC 2015-03, Vol.17 (3), p.1831-1841
Main Authors: Hogg, James M, Coleman, Fergal, Ferrer-Ugalde, Albert, Atkins, Martin P, Swadzba-Kwasny, Malgorzata
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container_title Green chemistry : an international journal and green chemistry resource : GC
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creator Hogg, James M
Coleman, Fergal
Ferrer-Ugalde, Albert
Atkins, Martin P
Swadzba-Kwasny, Malgorzata
description Liquid coordination complexes (LCCs) are a new class of liquid Lewis acids, prepared by combining an excess of a metal halide (e.g. GaCl sub(3)) with a basic donor molecule (e.g. amides, amines or phosphines). LCCs were used to catalyse oligomerisation of 1-decene to polyalphaolefins (PAOs). Molecular weight distribution and physical properties of the produced oils were compliant with those required for low viscosity synthetic (Group IV) lubricant base oils. Kinematic viscosities at 100 degree C of ca. 4 or 6 cSt were obtained, along with viscosity indexes above 120 and pour points below -57 degree C. In industry, to achieve similar properties, BF sub(3) gas is used as a catalyst. LCCs are proposed as a safer and economically attractive alternative to BF sub(3) gas for the production of polyalphaolefins.
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source Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)
subjects Coordination compounds
Lewis acid
Liquids
Metal halides
Molecular weight distribution
Natural gas
Phosphines
Viscosity
title Liquid coordination complexes: a new class of Lewis acids as safer alternatives to BF sub(3) in synthesis of polyalphaolefins
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