Brigita Bratić, Peter Altenbuchner, Thomas Heuser, Bernhard Rieger
{"title":"5-乙基-2-降冰片烯(ENB)和5-乙烯基-2-降冰片烯(VNB)基脂环多元醇合成聚酯","authors":"Brigita Bratić, Peter Altenbuchner, Thomas Heuser, Bernhard Rieger","doi":"10.1039/d5py00247h","DOIUrl":null,"url":null,"abstract":"Amorphous polyesters derived from rigid alicyclic monomers with high glass transition temperatures are of great interest as potential substitute for poly(carbonate)s. Therefore, 5-ethylidene-2-norbornene (ENB) and 5-vinyl-2-norbornene (VNB) were identified as interesting diol monomer precursors to enhance the thermal properties of polyesters. The regioselective synthesis of the corresponding diols from ENB and VNB were optimized and first scale up experiments gave promising results for a potential large scale production of these polyester monomers. Moreover, for proof of concept, an alternative procedure was established to synthesize exclusively branched diols. Polymerization experiments were conducted with dimethyl terephthalate (DMT) as model compound to compare the polyesters with commonly used poly(ethylene terephthalate)s. Therefore, a series of polyesters were produced containing branched or linear or a mixture of both regioisomers, and structure property relationships were investigated with GPC, TGA and DSC analysis. The Tg values ranged from 75 to 103 °C, depending on the branched and linear moieties in the polyester microstructure and their molecular weights. Moreover, isosorbide (IS) was introduced as biobased comonomer, resulting in amorphous copolyesters with promising Tgs ranging from 81 to 97 °C.","PeriodicalId":100,"journal":{"name":"Polymer Chemistry","volume":"79 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"5-Ethylidene-2-norbornene (ENB) and 5-Vinyl-2-norbornene (VNB) based Alicyclic Polyols for the Synthesis of Polyesters\",\"authors\":\"Brigita Bratić, Peter Altenbuchner, Thomas Heuser, Bernhard Rieger\",\"doi\":\"10.1039/d5py00247h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Amorphous polyesters derived from rigid alicyclic monomers with high glass transition temperatures are of great interest as potential substitute for poly(carbonate)s. Therefore, 5-ethylidene-2-norbornene (ENB) and 5-vinyl-2-norbornene (VNB) were identified as interesting diol monomer precursors to enhance the thermal properties of polyesters. The regioselective synthesis of the corresponding diols from ENB and VNB were optimized and first scale up experiments gave promising results for a potential large scale production of these polyester monomers. Moreover, for proof of concept, an alternative procedure was established to synthesize exclusively branched diols. Polymerization experiments were conducted with dimethyl terephthalate (DMT) as model compound to compare the polyesters with commonly used poly(ethylene terephthalate)s. Therefore, a series of polyesters were produced containing branched or linear or a mixture of both regioisomers, and structure property relationships were investigated with GPC, TGA and DSC analysis. The Tg values ranged from 75 to 103 °C, depending on the branched and linear moieties in the polyester microstructure and their molecular weights. Moreover, isosorbide (IS) was introduced as biobased comonomer, resulting in amorphous copolyesters with promising Tgs ranging from 81 to 97 °C.\",\"PeriodicalId\":100,\"journal\":{\"name\":\"Polymer Chemistry\",\"volume\":\"79 1\",\"pages\":\"\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-05-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5py00247h\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5py00247h","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
5-Ethylidene-2-norbornene (ENB) and 5-Vinyl-2-norbornene (VNB) based Alicyclic Polyols for the Synthesis of Polyesters
Amorphous polyesters derived from rigid alicyclic monomers with high glass transition temperatures are of great interest as potential substitute for poly(carbonate)s. Therefore, 5-ethylidene-2-norbornene (ENB) and 5-vinyl-2-norbornene (VNB) were identified as interesting diol monomer precursors to enhance the thermal properties of polyesters. The regioselective synthesis of the corresponding diols from ENB and VNB were optimized and first scale up experiments gave promising results for a potential large scale production of these polyester monomers. Moreover, for proof of concept, an alternative procedure was established to synthesize exclusively branched diols. Polymerization experiments were conducted with dimethyl terephthalate (DMT) as model compound to compare the polyesters with commonly used poly(ethylene terephthalate)s. Therefore, a series of polyesters were produced containing branched or linear or a mixture of both regioisomers, and structure property relationships were investigated with GPC, TGA and DSC analysis. The Tg values ranged from 75 to 103 °C, depending on the branched and linear moieties in the polyester microstructure and their molecular weights. Moreover, isosorbide (IS) was introduced as biobased comonomer, resulting in amorphous copolyesters with promising Tgs ranging from 81 to 97 °C.
期刊介绍:
Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.