A unified kinetic Monte Carlo approach to evaluate (a)symmetric block and gradient copolymers with linear and branched chains illustrated for poly(2-oxazoline)s. Issue 11 (25th February 2022)

• Record Type: Journal Article
• Authors: Conka, Robert; Marien, Yoshi W.; Sedlacek, Ondrej; Hoogenboom, Richard; Van Steenberge, Paul H. M.; D'hooge, Dagmar R.
• Is Part Of: Polymer chemistry. Volume 13:Issue 11(2022)
• Page Start: 1559
• Page End: 1575
• Publication Date: 2022-02-25
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/d1py01391b
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : Kinetic modeling is used to verify if PAOx synthesis routes can deliver ideal products such as (a)symmetric (block-)gradients and block copolymers. It is shown that a variation in chain length and topology affects the overall compositional deviation. Abstract : The synthesis of well-defined gradient, block-gradient and di-block copolymers with both asymmetric and symmetric compositions considering hydrophilic and hydrophobic monomer units is relevant for application fields, such as drug/gene delivery and (bio)compatibilization. The evaluation of the synthesis success and the resulting polymer structure remains however challenging, as ideally every chain needs to be considered, which is experimentally almost impossible. Matrix-based kinetic Monte Carlo ( k MC) simulations provide a solution to this challenge, as they allow to visualize the monomer sequences of individual chains with reliable parameter tuning based on experimental data on average compositions and size exclusion chromatography. Here, such matrix-based k MC simulations are applied to visualize monomer sequences in polymers prepared by living cationic ring-opening polymerization (CROP) of 2-methyl-2-oxazoline (MeOx) and 2-phenyl-2-oxazoline (PhOx), uniquely differentiating between linear and branched chains. For the branched chains, a novel modeling protocol is presented allowing to evaluate their structural (here compositional) organization in a similar manner as linear chains by comparing arm pairs. This delivers an average compositional deviation for these branched species (〈SDBr 〉) that in combination with the conventional deviation for linear chains (〈SDLin 〉) and proper weighing with the mass fractions allows to obtain the overall 〈SD〉. It is highlighted that di-block copolymer synthesis recipes most closely resemble the ideal target structure, benefiting from a semi-batch procedure. Such recipes allow to minimize the contribution of chain transfer to monomer and enable a more fluent transition of linear side products with bad composition in branched chains that by further growth can compensate for the compositional deviation. It is also demonstrated that reaching of the targeted structure is less trivial for a more symmetric composition and that (well-chosen) threshold 〈SD〉 values can be defined allowing to qualify synthesized copolymers as bad, good and excellent, at least for the guide of the eye. A sufficiently low dispersity is necessary to obtain a sufficiently high product quality, but as such is not a sufficient condition to evaluate the structural variation, highlighting the strength of the k MC framework for the identification of optimal synthesis protocols.