AI Article Synopsis

  • Precise control over polymer microstructure allows researchers to tailor material properties, but creating complex stereoblock polyesters from certain monomers has been challenging in polymer chemistry.
  • The study introduces irreversible chain-transfer ring-opening polymerization (ICT-ROP), which uses two catalysts with different stereoselectivities to achieve better control in synthesizing these complex polymers.
  • The researchers successfully produced atactic-syndiotactic stereoblock polyesters and polyhydroxyalkanoates, with notable control over various attributes that affect the physical properties of the final polymers.

Article Abstract

Precise control over polymer microstructure can enable the molecular tunability of material properties and represents a significant challenge in polymer chemistry. Stereoblock copolymers are some of the simplest stereosequenced polymers, yet the synthesis of stereoblock polyesters from prochiral or racemic monomers outside of "simple" isotactic stereoblocks remains limited. Herein, we report the development of irreversible chain-transfer ring-opening polymerization (ICT-ROP), which overcomes the fundamental limitations of single catalyst approaches by using transmetalation (e.g., alkoxide-chloride exchange) between two catalysts with distinct stereoselectivities as a means to embed temporally controlled multicatalysis in ROP. Our combined small-molecule model and catalytic polymerization studies lay out a clear molecular basis for ICT-ROP and are exploited to access the first examples of atactic-syndiotactic stereoblock (-sb-) polyesters, -sb- polyhydroxyalkanoates (PHAs). We achieve high levels of control over molecular weight, tacticity, monomer composition, and block structures in a temporally controlled manner and demonstrate that stereosequence control leads to polymer tensile properties that are independent of thermal properties.

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http://dx.doi.org/10.1021/jacs.4c02976DOI Listing

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Article Synopsis
  • Precise control over polymer microstructure allows researchers to tailor material properties, but creating complex stereoblock polyesters from certain monomers has been challenging in polymer chemistry.
  • The study introduces irreversible chain-transfer ring-opening polymerization (ICT-ROP), which uses two catalysts with different stereoselectivities to achieve better control in synthesizing these complex polymers.
  • The researchers successfully produced atactic-syndiotactic stereoblock polyesters and polyhydroxyalkanoates, with notable control over various attributes that affect the physical properties of the final polymers.
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Organocatalyzed ring-opening polymerization is a powerful tool for the synthesis of a variety of functional, readily degradable polyesters and polycarbonates. We report the use of (thio)ureas in combination with cyclopropenimine bases as a unique catalyst for the polymerization of cyclic esters and carbonates with a large span of reactivities. Methodologies of exceptionally effective and selective cocatalyst combinations were devised to produce polyesters and polycarbonates with narrow dispersities ( = 1.

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Highly Active Organocatalysts for Stereoselective Ring-Opening Polymerization of Racemic Lactide at Room Temperature.

ACS Macro Lett

October 2022

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Although significant advances have been achieved, highly stereocontrolled polymerization using organocatalysts is still a great challenge, such as ring-opening polymerization of racemic lactide (-LA) for the synthesis of stereoregular polylactide (PLA). In this context, a series of binary organocatalysts consisting of different phosphazenes (CTPB, CN-Me-P, CN-Py-P, -BuP, and -BuP) and achiral ureas (U1-U6) were applied for the stereocontrolled ROP of -LA under mild conditions. It is remarkable that CN-Py-P/U4 with the compatible basicity/acidity showed both high activity (92% conversion within 10 min) and great stereoselectivity ( = 0.

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