Joshua T. Kamps, Bruce E. Kirkpatrick, Sean P. Keyser, Connor E. Miksch, Benjamin R. Nelson, John F. Rynk, Benjamin D. Fairbanks, Kristi S. Anseth, Christopher N. Bowman
{"title":"Linear and Network-Forming Acetal Polymerization of Multifunctional Alcohols with Dichloromethane for Degradable and Recyclable Materials","authors":"Joshua T. Kamps, Bruce E. Kirkpatrick, Sean P. Keyser, Connor E. Miksch, Benjamin R. Nelson, John F. Rynk, Benjamin D. Fairbanks, Kristi S. Anseth, Christopher N. Bowman","doi":"10.1021/acs.macromol.4c03078","DOIUrl":null,"url":null,"abstract":"Although thermoplastic and thermoset materials have revolutionized modern living, their widespread use has also led to significant environmental challenges due to limited recyclability and persistence in the environment. To address these issues, the development of new materials that are both functional and sustainable is crucial. In this work, an acetal-based polymerization is demonstrated, wherein dichloromethane (DCM) serves as a methylene synthon for forming acetals between alcohol end groups in the presence of a strong base, facilitating the production of fully degradable polymers and networks, as well as facile recovery of repolymerizable monomers. The incorporation of functional groups via primary alcohols, such as norbornene methanol, enables simultaneous functionalization of the polymer structure. Glycol-based linear polymers and macromers are utilized as primary building blocks, offering a versatile platform for generating tunable polymer architectures. Additionally, acetal-based oligomerization of decanediol is achieved at increased temperature and pressure, broadening the scope of potential materials accessible through this method. This historically understudied reaction holds great promise for the design of functional, degradable, and recyclable polymers.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"59 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.4c03078","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Although thermoplastic and thermoset materials have revolutionized modern living, their widespread use has also led to significant environmental challenges due to limited recyclability and persistence in the environment. To address these issues, the development of new materials that are both functional and sustainable is crucial. In this work, an acetal-based polymerization is demonstrated, wherein dichloromethane (DCM) serves as a methylene synthon for forming acetals between alcohol end groups in the presence of a strong base, facilitating the production of fully degradable polymers and networks, as well as facile recovery of repolymerizable monomers. The incorporation of functional groups via primary alcohols, such as norbornene methanol, enables simultaneous functionalization of the polymer structure. Glycol-based linear polymers and macromers are utilized as primary building blocks, offering a versatile platform for generating tunable polymer architectures. Additionally, acetal-based oligomerization of decanediol is achieved at increased temperature and pressure, broadening the scope of potential materials accessible through this method. This historically understudied reaction holds great promise for the design of functional, degradable, and recyclable polymers.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.