Atactic, Isotactic, and Syndiotactic Methylated Polyhydroxybutyrates: An Unexpected Series of Isomorphic Polymers

Polyhydroxyalkanoates (PHAs), such as poly[(R)-3-hydroxybutyrates] [(R)-P3HB], are produced by bacteria and are promising alternatives to nondegradable polyolefin plastics, but their semicrystallinity and high melting points are only maintained at high tacticity, which are commonly seen in other semicrystalline polymers like isotactic polypropylene (iPP). We herein report a class of synthetic PHAs, cis-poly(3-hydroxy-2-methylbutyrate)s (cis-PHMBs), that exhibit tacticity-independent semicrystallinity. The syndiotactic, isotactic, and even atactic PHMBs all share high melting points (Tm > 170 °C) and nearly identical crystal structures. The isomorphism of these polymers across three different tacticities has allowed access to iPP-like, high-performance PHMB without the requirement of high tacticity

Regioselective Isomerization of 2,3-Disubstituted Epoxides to Ketones: An Alternative to the Wacker Oxidation of Internal Alkenes

We report an alternative pathway to the Wacker oxidation of internal olefins involving epoxidation of <i>trans</i>-alkenes followed by a mild and highly regioselective isomerization to give the major ketone isomers in 66–98% yield. Preliminary kinetics and isotope labeling studies suggest epoxide ring opening as the turnover limiting step in our proposed mechanism. A similar catalytic system was applied to the kinetic resolution of select <i>trans</i>-epoxides to give synthetically useful selectivity factors of 17–23 for benzyl-substituted substrates

Carbonylation of Ethylene Oxide to β‑Propiolactone: A Facile Route to Poly(3-hydroxypropionate) and Acrylic Acid

We report an improved synthesis of poly­(3-hydroxypropionate) (P3HP) from ethylene oxide (EO) and carbon monoxide (CO) through the intermediate β-propiolactone (PL). The optimized carbonylation of EO resulted in high selectivity for PL using a bimetallic [Lewis acid]⁺[Co­(CO)₄]⁻ catalyst. Anionic ring-opening polymerization of PL by organic ionic compounds to afford P3HP was also investigated. A phosphazenium carboxylate initiator displays the highest activity for the polymerization and produces polyesters with molecular weights over 100 kDa and narrow molar mass distributions. Furthermore, the known rearrangement of PL and the thermolysis of P3HP provide efficient EO-based routes to the important commodity chemical acrylic acid

Tailored Living Block Copolymerization: Multiblock Poly(cyclohexene carbonate)s with Sequence Control

Tailored Living Block Copolymerization: Multiblock Poly(cyclohexene carbonate)s with Sequence Contro

Chemically Recyclable Ester-Linked Polypropylene

Polyolefins represent the largest class of commodity materials due to their excellent material properties; however, they have limited pathways to chemical recycling and are often difficult to mechanically recycle. Here we demonstrate a new catalyst for the isoselective copolymerization of propylene and butadiene capable of favoring 1,4-insertion over 1,2-insertion while maintaining good molecular weights and turnover frequencies. This isotactic propylene copolymer with main-chain unsaturation was depolymerized to a telechelic macromonomer using an olefin metathesis catalyst and 2-hydroxyethyl acrylate. After hydrogenation, the telechelic macromonomer was repolymerized to form an ester-linked polypropylene material. This polymer shows thermal and mechanical properties comparable to linear low-density polyethylene. Finally, the telechelic macromonomer could be regenerated through the depolymerization of the ester-linked polypropylene material, which allows for the chemical recycling to macromonomer. This process provides a route to transform partially unsaturated polyolefins to chemically recyclable materials with similar properties to their parent polymers

Chain-Straightening Polymerization of Olefins to Form Polar Functionalized Semicrystalline Polyethylene

We report the design and synthesis of an α-diimine PdII catalyst that copolymerizes functionalized and long chain α-olefins to produce semicrystalline polyethylene materials. Through a chain-straightening polymerization mechanism, the catalyst afforded high-melting point polymers with Tm values of up to 120 °C. The chain-straightening polymerization operates with high [ω,1]-insertion selectivity at high alkene concentrations and with varying α-olefin chain lengths, including propylene. The Pd catalyst can copolymerize 1-decene and methyl decenoate into semicrystalline ester-functionalized polymers with incorporation percentages proportional to the comonomer ratio (up to 13 mol %). 13C nuclear magnetic resonance and isotope labeling studies revealed that the improved selectivity relative to those of other systems arises from a high selectivity for [2,1]-insertion (96%) coupled with rapid chain-walking for a total of 90 mol % of 1-decene undergoing net [10,1]-insertion

Mechanistic Insight into Thiophene Catalyst-Transfer Polymerization Mediated by Nickel Diimine Catalysts

Catalyst-transfer polymerization (CTP) is a living, chain-growth method for accessing conjugated polymers with control over their length and sequence. Typical catalysts utilized in CTP are either Pd or Ni complexes with bisphosphine or N-heterocyclic carbene ancillary ligands. More recently, diimine-ligated Ni complexes have been employed; however, in most cases nonliving pathways become dominant at high monomer conversions and/or low catalyst loading. We report herein an alternative Ni diimine catalyst that polymerizes 3-hexylthiophene in a chain-growth manner at low catalyst loading and high monomer conversion. In addition, we elucidate the chain-growth mechanism as well as one chain-transfer pathway. Overall, these studies provide insight into the mechanism of conjugated polymer synthesis mediated by Ni diimine catalysts

Controlled Chain Walking for the Synthesis of Thermoplastic Polyolefin Elastomers: Synthesis, Structure, and Properties

Thermoplastic elastomers are attractive materials because of their ability to be melt-processed, reused, and recycled, unlike chemically cross-linked elastomers such as rubber. We report the synthesis and mechanical properties of polyolefin-based thermoplastic elastomer block copolymers. A simple one-pot procedure is employed, using a living arylnaphthyl-α-diimine Ni­(II) “sandwich” complex to generate high crystallinity hard blocks from 1-decene and low crystallinity soft blocks from ethylene. Various block structures are accessed, ranging from a diblock up to a heptablock copolymer. Statistical copolymers of 1-decene and ethylene are also synthesized for comparison. All resulting polymers behave as elastomers, with properties that modulate with hard and soft block composition, block architecture, and polymerization solvent. Triblock copolymers demonstrate strain at break values up to 750%, with elastic strain recoveries up to 85%. Interestingly, statistical copolymers demonstrate strain at break values upward of 1120% and elastic strain recoveries up to 77%. Creep experiments were performed to determine the resilience of these materials to deformation. It is found that higher block architectures (triblock and above) have greater resistance to strain-induced deformation than lower block architectures (diblock and statistical)

Chain-Straightening Polymerization of Olefins to Form Polar Functionalized Semicrystalline Polyethylene

We report the design and synthesis of an α-diimine PdII catalyst that copolymerizes functionalized and long chain α-olefins to produce semicrystalline polyethylene materials. Through a chain-straightening polymerization mechanism, the catalyst afforded high-melting point polymers with Tm values of up to 120 °C. The chain-straightening polymerization operates with high [ω,1]-insertion selectivity at high alkene concentrations and with varying α-olefin chain lengths, including propylene. The Pd catalyst can copolymerize 1-decene and methyl decenoate into semicrystalline ester-functionalized polymers with incorporation percentages proportional to the comonomer ratio (up to 13 mol %). 13C nuclear magnetic resonance and isotope labeling studies revealed that the improved selectivity relative to those of other systems arises from a high selectivity for [2,1]-insertion (96%) coupled with rapid chain-walking for a total of 90 mol % of 1-decene undergoing net [10,1]-insertion