{"title":"Embedding Mo2O2S2-Bis(thiosemicarbazone) Complexes Into Polyurethane Matrices: Synthesis and Characterization","authors":"Diana Cebotari, Roa AlChamandi, Yann Molard, Maria Amela-Cortes, Carine Livage, Mohamed Haouas, Jérôme Marrot, Aurelian Gulea, Cyril Gorny, Bruno Fayolle, Sergiu Calancea, Sébastien Floquet","doi":"10.1002/pol.20240556","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>[Mo<sup>V</sup>\n <sub>2</sub>O<sub>2</sub>S<sub>2</sub>]<sup>2+</sup>-based thiosemicarbazone complexes are an interesting family of molecules, which can display various biological properties. However, in order to develop applications, it is necessary to shape this type of complex, in polymer matrices for example. In this article, we report the synthesis of a series of 16 composite materials corresponding to the incorporation of [(Mo<sub>2</sub>O<sub>2</sub>S<sub>2</sub>)<sub>\n <i>n</i>\n </sub>(L<sup>1–6</sup>)<sub>\n <i>n</i>\n </sub>] (<i>n</i> = 1, 2) bis-thiosemicarbazones complexes in a polyurethane matrix. These composites are described as [Mo<sup>V</sup>\n <sub>2</sub>O<sub>2</sub>S<sub>2</sub>]<sup>2+</sup>–thiosemicarbazone-based polyurethanes and denoted PU-[(Mo<sub>2</sub>O<sub>2</sub>S<sub>2</sub>)<sub>\n <i>n</i>\n </sub>(L<sup>1–6</sup>)<sub>\n <i>n</i>\n </sub>] (<i>n</i> = 1, 2). Various [(Mo<sub>2</sub>O<sub>2</sub>S<sub>2</sub>)<sub>\n <i>n</i>\n </sub>(L<sup>1–6</sup>)<sub>\n <i>n</i>\n </sub>]–bis-thiosemicarbazone complexes were used including di- or tetranuclear structures with different numbers of uncoordinated amino and hydroxyl groups and alkyl substituents on the ligands L<sup>\n <i>i</i>\n </sup> (<i>i</i> = 1–6). The composite materials obtained are studied in depth by SEM–EDX, FT-IR, NMR, TGA, and DSC to understand the organization of polymer chains and complexes within the materials and to highlight certain changes in physical properties induced by the nature of the complexes. The complexes are homogeneously distributed within the polymer matrices and the embedding of these complexes seems to be mainly due to hydrogen bonding networks. Nevertheless, these H-bond networks are strong enough to provoke modification of the physical properties of the polymers in terms of thermal stability or flexibility.</p>\n </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"63 8","pages":"1760-1773"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/pol.20240556","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
[MoV2O2S2]2+-based thiosemicarbazone complexes are an interesting family of molecules, which can display various biological properties. However, in order to develop applications, it is necessary to shape this type of complex, in polymer matrices for example. In this article, we report the synthesis of a series of 16 composite materials corresponding to the incorporation of [(Mo2O2S2)n(L1–6)n] (n = 1, 2) bis-thiosemicarbazones complexes in a polyurethane matrix. These composites are described as [MoV2O2S2]2+–thiosemicarbazone-based polyurethanes and denoted PU-[(Mo2O2S2)n(L1–6)n] (n = 1, 2). Various [(Mo2O2S2)n(L1–6)n]–bis-thiosemicarbazone complexes were used including di- or tetranuclear structures with different numbers of uncoordinated amino and hydroxyl groups and alkyl substituents on the ligands Li (i = 1–6). The composite materials obtained are studied in depth by SEM–EDX, FT-IR, NMR, TGA, and DSC to understand the organization of polymer chains and complexes within the materials and to highlight certain changes in physical properties induced by the nature of the complexes. The complexes are homogeneously distributed within the polymer matrices and the embedding of these complexes seems to be mainly due to hydrogen bonding networks. Nevertheless, these H-bond networks are strong enough to provoke modification of the physical properties of the polymers in terms of thermal stability or flexibility.
期刊介绍:
Journal of Polymer Research provides a forum for the prompt publication of articles concerning the fundamental and applied research of polymers. Its great feature lies in the diversity of content which it encompasses, drawing together results from all aspects of polymer science and technology.
As polymer research is rapidly growing around the globe, the aim of this journal is to establish itself as a significant information tool not only for the international polymer researchers in academia but also for those working in industry. The scope of the journal covers a wide range of the highly interdisciplinary field of polymer science and technology.