{"title":"基于三氟丙基取代三硅烷醇的分子明确硅树脂的制备及其热、机械和抗紫外线性能","authors":"Miku Kosaka, Taishi Nakano, Kenji Kanaori, Hiroaki Imoto, Kensuke Naka","doi":"10.1038/s41428-024-00886-w","DOIUrl":null,"url":null,"abstract":"We prepared flexible free-standing films of trifluoropropyl-substituted open-cage silsesquioxane-pendant polysiloxane by optimizing the sol-gel reaction conditions of tris(dimethoxysilyl-ethyl-dimethylsiloxy)-heptatrifluoropropyl-substituted open-cage silsesquioxane (1). The polycondensation of 1 was fully achieved even at 50 °C for 6 h under vacuo. 29Si CP-MAS NMR analysis indicated that the flexible free-standing films, polycondensed at 50 °C and 180 °C, included cyclotrisiloxane (D3) and linear siloxane (Dlinear) structures. The elastic modulus and decomposition temperature at 5% mass weight loss (Td5) of the product by polycondensation at 180 °C under N2 were significantly greater than those for the 50 °C product. Significant changes in the UV‒vis spectra of the resulting transparent films were not observed even after 13 days of UV irradiation in air. In contrast, UV irradiation of the isobutyl-substituted counterpart under air clearly caused a decrease in its transmittance due to autoxidative degradation. Free-standing films of trifluoropropyl-substituted open-cage silsesquioxane-pendant polysiloxane by optimizing sol-gel reaction condition of tris(dimethoxysilyl-ethyl-dimethylsiloxy)-heptatrifluoropropyl-substituted open-cage silsesquioxane. Elastic modulus and the decomposition temperature for 5% weight loss under N2 of the product by polycondensation at 180 °C were significantly higher than that by polycondensation at 50 °C. Significant changes in the UV-vis spectra of the resulting transparent films were hardly observed even after 13 days of UV irradiation.","PeriodicalId":20302,"journal":{"name":"Polymer Journal","volume":"56 5","pages":"481-489"},"PeriodicalIF":2.3000,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation of molecularly well-defined silicone resins based on trifluoropropyl-substituted trisilanol and their thermal, mechanical, and UV-resistance properties\",\"authors\":\"Miku Kosaka, Taishi Nakano, Kenji Kanaori, Hiroaki Imoto, Kensuke Naka\",\"doi\":\"10.1038/s41428-024-00886-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We prepared flexible free-standing films of trifluoropropyl-substituted open-cage silsesquioxane-pendant polysiloxane by optimizing the sol-gel reaction conditions of tris(dimethoxysilyl-ethyl-dimethylsiloxy)-heptatrifluoropropyl-substituted open-cage silsesquioxane (1). The polycondensation of 1 was fully achieved even at 50 °C for 6 h under vacuo. 29Si CP-MAS NMR analysis indicated that the flexible free-standing films, polycondensed at 50 °C and 180 °C, included cyclotrisiloxane (D3) and linear siloxane (Dlinear) structures. The elastic modulus and decomposition temperature at 5% mass weight loss (Td5) of the product by polycondensation at 180 °C under N2 were significantly greater than those for the 50 °C product. Significant changes in the UV‒vis spectra of the resulting transparent films were not observed even after 13 days of UV irradiation in air. In contrast, UV irradiation of the isobutyl-substituted counterpart under air clearly caused a decrease in its transmittance due to autoxidative degradation. Free-standing films of trifluoropropyl-substituted open-cage silsesquioxane-pendant polysiloxane by optimizing sol-gel reaction condition of tris(dimethoxysilyl-ethyl-dimethylsiloxy)-heptatrifluoropropyl-substituted open-cage silsesquioxane. Elastic modulus and the decomposition temperature for 5% weight loss under N2 of the product by polycondensation at 180 °C were significantly higher than that by polycondensation at 50 °C. 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引用次数: 0
摘要
我们通过优化三(二甲氧基硅基-乙基-二甲基硅氧基)-七三氟丙基取代开式笼状硅倍半氧烷(1)的溶胶-凝胶反应条件,制备出了三氟丙基取代开式笼状硅倍半氧烷的柔性独立薄膜。1 在 50 °C 的真空条件下缩聚 6 小时即可完全缩聚。29Si CP-MAS NMR 分析表明,在 50 °C 和 180 °C 下缩聚的柔性独立薄膜包括环三硅氧烷(D3)和线性硅氧烷(Dlinear)结构。在氮气环境下于 180 ℃ 缩聚生成的产品的弹性模量和质量损失 5% 时的分解温度(Td5)明显高于 50 ℃ 的产品。即使在空气中经过 13 天的紫外线照射,也没有观察到透明薄膜的紫外可见光谱发生明显变化。相反,由于自氧化降解,在空气中紫外线照射异丁基取代物明显导致其透射率下降。
Preparation of molecularly well-defined silicone resins based on trifluoropropyl-substituted trisilanol and their thermal, mechanical, and UV-resistance properties
We prepared flexible free-standing films of trifluoropropyl-substituted open-cage silsesquioxane-pendant polysiloxane by optimizing the sol-gel reaction conditions of tris(dimethoxysilyl-ethyl-dimethylsiloxy)-heptatrifluoropropyl-substituted open-cage silsesquioxane (1). The polycondensation of 1 was fully achieved even at 50 °C for 6 h under vacuo. 29Si CP-MAS NMR analysis indicated that the flexible free-standing films, polycondensed at 50 °C and 180 °C, included cyclotrisiloxane (D3) and linear siloxane (Dlinear) structures. The elastic modulus and decomposition temperature at 5% mass weight loss (Td5) of the product by polycondensation at 180 °C under N2 were significantly greater than those for the 50 °C product. Significant changes in the UV‒vis spectra of the resulting transparent films were not observed even after 13 days of UV irradiation in air. In contrast, UV irradiation of the isobutyl-substituted counterpart under air clearly caused a decrease in its transmittance due to autoxidative degradation. Free-standing films of trifluoropropyl-substituted open-cage silsesquioxane-pendant polysiloxane by optimizing sol-gel reaction condition of tris(dimethoxysilyl-ethyl-dimethylsiloxy)-heptatrifluoropropyl-substituted open-cage silsesquioxane. Elastic modulus and the decomposition temperature for 5% weight loss under N2 of the product by polycondensation at 180 °C were significantly higher than that by polycondensation at 50 °C. Significant changes in the UV-vis spectra of the resulting transparent films were hardly observed even after 13 days of UV irradiation.
期刊介绍:
Polymer Journal promotes research from all aspects of polymer science from anywhere in the world and aims to provide an integrated platform for scientific communication that assists the advancement of polymer science and related fields. The journal publishes Original Articles, Notes, Short Communications and Reviews.
Subject areas and topics of particular interest within the journal''s scope include, but are not limited to, those listed below:
Polymer synthesis and reactions
Polymer structures
Physical properties of polymers
Polymer surface and interfaces
Functional polymers
Supramolecular polymers
Self-assembled materials
Biopolymers and bio-related polymer materials
Polymer engineering.