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.4c02976 | DOI Listing |
J Am Chem Soc
April 2024
Department of Chemistry, Brown University, 324 Brook St., Providence, Rhode Island 02912, United States.
ACS Macro Lett
January 2024
IBM Almaden Research Center, San Jose, California 95120, United States.
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.
View Article and Find Full Text PDFACS Macro Lett
October 2023
Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455-0431, United States of America.
Star block (ABC) terpolymers consisting of a rubbery poly(γ-methyl-ε-caprolactone) (PγMCL) (C) core and hard poly(l-lactide) (PLLA) (B) and poly(d-lactide) (PDLA) (A) end-blocks with varying PDLA to PLLA block ratios were explored as high-performance, sustainable, aliphatic polyester thermoplastic elastomers (APTPEs). The stereocomplexation of the PDLA/PLLA blocks within the hard domains provided the APTPEs with enhanced thermal stability and an increased resistance to permanent deformation compared to nonstereocomplex analogs. Variations in the PDLA:PLLA block ratio yielded tunable mechanical properties likely due to differences in the extent and location of stereocomplex crystallite formation as a result of architectural constraints.
View Article and Find Full Text PDFACS Macro Lett
October 2022
Key Laboratory of Biobased Polymer Materials, College of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao, 266042, China.
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.
View Article and Find Full Text PDFChem Sci
January 2021
Department of Chemical Engineering, Virginia Polytechnic Institute and State University 635 Prices Fork Road, Blacksburg Virginia 24061 USA
Photoredox ring-opening polymerization of -carboxyanhydrides allows for the synthesis of polyesters with precisely controlled molecular weights, molecular weight distributions, and tacticities. While powerful, obviating the use of precious metal-based photocatalysts would be attractive from the perspective of simplifying the protocol. Herein, we report the Co and Zn catalysts that are activated by external light to mediate efficient ring-opening polymerization of -carboxyanhydrides, without the use of exogenous precious metal-based photocatalysts.
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