Catalysts for the Controlled Polymerization of Conjugated Dienes

Nowadays, there is a better understanding of the polymerization mechanism and involves allyl-active species, thanks in particular to the support of more and more efficient calculations methods [9,10,11]. Since the beginning of the 2000s, there has also been a tendency for statistical copolymerizatio...

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Published inCatalysts Vol. 8; no. 10; p. 442
Main Author Visseaux, Marc
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 01.10.2018
MDPI
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Summary:Nowadays, there is a better understanding of the polymerization mechanism and involves allyl-active species, thanks in particular to the support of more and more efficient calculations methods [9,10,11]. Since the beginning of the 2000s, there has also been a tendency for statistical copolymerization of 1,3-dienes with olefin or styrene comonomers to produce statistical, alternating, and block copolymers [12], while access to multiblock and stereoblock copolymers is currently made possible by the innovative approaches of coordinative chain transfer polymerization [13]. [...]the future will probably see the development of alternative catalysts made from non-toxic and abundant metals like iron, while an even greater interest can be expected for rare earth catalysts following the discovery of new geological resources of these elements [14]. Particular behavior was observed vs. polymerization, related in particular to the internal or external substitution of the substrate diene monomer, also depending on the molecular structure (exo-exo or exo-endo orientation of the allyl group and steric bulk of additional phosphine ligands) of the pre-catalyst. [...]our group contributed under the form of a mini-review, which focuses on the recent advances on the synthesis, structure, and characterization of allyl-based rare earth organometallic complexes, with emphasis on their ability to catalyze the polymerization of non-polar monomers such as conjugated dienes, styrene, and their related copolymerization [21].
Bibliography:SourceType-Scholarly Journals-1
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ObjectType-Editorial-2
ObjectType-Commentary-1
ISSN:2073-4344
2073-4344
DOI:10.3390/catal8100442