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Alternating copolymers are distinctly unique in comparison with other copolymers. Herein, an in-depth investigation of the oxyanionic ring-opening copolymerization of propylene oxide (PO) and allyl glycidyl ether (AGE) from benzyl alcohol (BnOH) activated with potassium acetate (KOAc) complexed by 18-crown-6 ether (18C6) is described. We demonstrate that the 18C6/KOAc complex is an efficient and benign catalytic system to promote copolymerization of both oxirane monomers, leading to well-defined polyethers with varied comonomer content and low dispersity values (ƉM < 1.20). Kinetic analysis confirmed the controlled nature of the (co)polymerization process, and the determination of reactivity ratios revealed a quasi-alternating copolymerization profile, according to the Fineman-Ross method. The comparison between the quasi-alternating-type PO/AGE copolymerization and block or gradient copolymerization revealed significant differences, to confirm the different sequence incorporation in the different topological copolymers. These results highlight the great potential of 18C6/KOAc-mediated copolymerization process for the controlled sythesis of a series of copolymer topologies. all: To meet the rising demand for sustainable and simple polymer syntheses, organocatalytic polymerizations are a powerful tool. Here, the authors report the quasi-alternating polymerization of oxirane monomers at room temperature and in solvent-free conditions catalyzed by potassium acetate complexed by 18-crown-6 ether, leading to well-defined polyethers with varied comonomer content and low dispersity values. [ABSTRACT FROM AUTHOR]

The oxyanionic ring‐opening polymerization of propylene oxide (PO) from an exogenous alcohol activated with benign (complexed) metal‐alkali carboxylates is described. The equimolar mixture of potassium acetate (KOAc) and 18‐crown‐6 ether (18C6) is demonstrated to be the complex of choice for preparing poly(propylene oxide) (PPO) in a controlled manner. In the presence of 18C6/KOAc, hydrogen‐bonded alcohols act as soft nucleophiles promoting the PO SN2 process at room temperature and in solvent‐free conditions while drastically limiting the occurrence of parasitic hydrogen abstraction generally observed during the anionic ROP of PO. The resulting PPO displays predictable and unprecedented molar masses (up to 20 kg mol−1) with low dispersities (ĐM < 1.1), rendering the 18C6/KOAc complex the most performing activator for the oxyanionic polymerization of PO reported to date. Preliminary studies on the preparation of block and statistical copolyethers are also reported. [ABSTRACT FROM AUTHOR]

Thiol-ene/−yne click reactions can be a versatile toolbox for the design and modification of polymers, enhancing functionality and providing opportunities for the development of innovative materials and applications. Here, we report a simple strategy to synthesize alkoxysilyl telechelic poly(propylene oxide)s (PPO)s: a) through a post-polymerization functionalization via Williamson reactions, commercial PPO is modified at the chain-end secondary alcohols with allyl or propargyl units, achieving >99% conversion; b) subsequent click reactions of (3-mercaptopropyl)trimethoxysilane (MPTMS), triggered by thermal and photochemical radical initiators, result in the incorporation of alkoxysilane groups on the polyether chain. Both thermal and photochemical thiol-ene/−yne click pathways are robust methodologies for preparing alkoxysilyl-modified PPOs in excellent yields (> 99%). Optimal conditions were identified as solvent-free, at 65 °C with 2,2′-azobis(2-methylpropionitrile) (AIBN) as the radical source. Detailed NMR analyses confirm the quantitative transformation of vinyl/propargyl functionalities in the resulting alkoxysilyl telechelic PPOs. Preliminary studies on the stability of alkoxysilyl end-groups are reported using 29Si NMR spectroscopy. [Display omitted] • (Multi)functional alkoxysilyl-modified polyethers were prepared and characterized. • Solvent-free thiol-ene/−yne click processes • Quantitative evaluation of the degree of end-functionalization by NMR spectroscopy • The resulting silyl-functionalized polymers showed good stability over time. [ABSTRACT FROM AUTHOR]

Controlled Oxyanionic Polymerization of Propylene Oxide: Unlocking the Molecular-Weight Limitation by a Soft Nucleophilic Catalysis In its presence, alcohols act as soft nucleophiles promoting a perfectly controlled oxyanionic polymerization at room temperature and in bulk leading to polymers displaying predictable and unprecedented molar masses. B Front Cover b : Article 2200424 by Olivier Coulembier and co-workers reveals that an equimolar mixture of potassium acetate and 18-crown-6 ether is highly effective for controlling the polymerization of propylene oxide. [Extracted from the article]