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Abstract The synthesis of vinyl alcohol copolymers is limited due to the poor radical reactivity of vinyl acetate (VAc), the traditional precursor to polyvinyl alcohol (PVA). Main group monomers such as BN 2‐vinylnaphthalene (BN2VN) have attracted attention as alternatives to VAc to form side chain hydroxyls via oxidation, but outstanding questions of molecular weight control remain. Herein we report systematic investigation of solvent, temperature, and initiator concentration as factors influencing BN2VN degree of polymerization. We find increased chain transfer to toluene, hypothesized to arise from differences in radical stabilization and reactivity by aromatic and BN aromatic rings. As a result of these combined efforts, high molecular weight (Mw ~ 105 g mol−1) BN2VN homopolymers and BN2VN‐styrene copolymers were obtained.
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RAFT Polymerization of an Aromatic Organoborane for Block Copolymer Synthesis
Synthesizing polystyrene-block-poly(vinyl alcohol) (PS-b-PVA) via controlled radical polymerization of vinyl acetate, the traditional precursor to polyvinyl alcohol (PVA), is challenging due to the reactivity of the unconjugated α-acetoxy radical. We report the synthesis and characterization of PS-b-PVA block copolymers (BCPs) with tailorable PVA block lengths via RAFT polymerization of an alternative precursor, an aromatic organoborane comonomer BN 2-vinylnapthalene (BN2VN). RAFT homopolymerization of BN2VN (RB) using 2-cyano-2-propyl dodecyl trithiocarbonate (CPDT) is described. Solid-state NMR, ATR-IR, SEC and thermogravimetric analysis reveal significant differences between PS-b-PVA and RS-b-RB. The fate of the trithiocarbonate end-group during oxidative conversion of the C–B side chain to a C–OH side chain was studied; while a hydrated aldehyde (e.g., gem-diol) was hypothesized, conclusive evidence was not found.
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- PAR ID:
- 10462027
- Date Published:
- Journal Name:
- Polymer Chemistry
- ISSN:
- 1759-9954
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/D3PY00706E
