Jump to main content
Jump to site search

Issue 13, 2019
Previous Article Next Article

Polymerization of cystine-derived monomers

Author affiliations

Abstract

Cystine was used as a platform chemical to prepare cyclic and acyclic monomers for entropy-driven ring-opening polymerization (ED-ROMP) via olefin or disulfide metathesis and for step-growth polymerization. The olefin ED-ROMP of an olefin/disulfide containing 16-atom macrocycle using the 3rd generation Grubbs catalyst was examined in greater detail. Kinetic studies revealed that the catalyst turned inactive during the polymerization, which limited the achievable (apparent) polymer molar mass to ∼70 kg mol−1. Such limitation could be overcome with the disulfide ED-ROMP of the same macrocycle to yield polymers with molar masses of up to 180 kg mol−1. The step-growth polymerizations of acyclic diene and dithiol monomers via olefin metathesis or oxidation were far less effective and yielded just low molar mass polymers or oligomers; photopolymerization of a thiol–ene monomer produced a polyester with a molar mass of 35 kg mol−1.

Graphical abstract: Polymerization of cystine-derived monomers

Back to tab navigation

Article information


Submitted
24 Jan 2019
Accepted
13 Feb 2019
First published
13 Feb 2019

Polym. Chem., 2019,10, 1636-1641
Article type
Paper

Polymerization of cystine-derived monomers

F. N. Behrendt, A. Hess, M. Lehmann, B. Schmidt and H. Schlaad, Polym. Chem., 2019, 10, 1636
DOI: 10.1039/C9PY00118B

Social activity

Search articles by author

Spotlight

Advertisements