Volume 59, Issue 12 pp. 4743-4749
Research Article

Branching Regulation in Olefin Polymerization via Lewis Acid Triggered Isomerization of Monomers

Hatice E. Basbug Alhan

Hatice E. Basbug Alhan

Department of Chemistry, Center of Excellence in Polymer Chemistry, University of Houston, 3585 Cullen Blvd., Houston, TX, 77204 USA

Search for more papers by this author
Dr. Glen R. Jones

Corresponding Author

Dr. Glen R. Jones

Department of Chemistry, Center of Excellence in Polymer Chemistry, University of Houston, 3585 Cullen Blvd., Houston, TX, 77204 USA

Search for more papers by this author
Prof. Eva Harth

Corresponding Author

Prof. Eva Harth

Department of Chemistry, Center of Excellence in Polymer Chemistry, University of Houston, 3585 Cullen Blvd., Houston, TX, 77204 USA

Search for more papers by this author
First published: 27 December 2019
Citations: 28

Graphical Abstract

Branch manager: Addition of AlCl3 to a Pd-mediated chain-walking polymerization results in rapid isomerization of 1-alkenes to internal alkenes which polymerize with high branching. Block copolymers can be prepared by adding AlCl3 midway through the reaction.

Abstract

We present a new strategy to regulate branching in chain-walking olefin polymerization by triggering a rapid isomerization of 1-alkene monomers into internal olefins by adding a Lewis acid. Polymerization of internal alkenes proceeds via chain-walking to give polymers with much higher branching than 1-alkene analogues. The utility of this approach is exemplified by synthesis of well-defined block copolymers with distinct branching characteristics per block by addition of Lewis acid midway through a reaction. We propose a novel mechanism whereby Lewis acid undergoes a counterion swap with the complex which favors isomerization as well as forming adducts with ancillary ligands, freeing coordination sites for internal alkene coordination polymerization.

Conflict of interest

The authors declare no conflict of interest.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.