{"title":"施-受体Stenhouse加合物后合成光致变色微粒。","authors":"Yinghao Ji,Fanxi Sun,Gaolu Zhu,Bo Han,Yuxuan Zhao,Daisheng Yang,Xu Deng,Longquan Chen,Yonghao Zheng,Chen Wei,Dongsheng Wang","doi":"10.1021/acsami.5c04468","DOIUrl":null,"url":null,"abstract":"Encapsulating photoresponsive molecules into polymers is an effective strategy to achieve fast and efficient photochromism in the solid state. Water is often used as the dispersion phase for the formation of polymeric microparticles; however, it reacts with the photoresponsive molecules and induces irreversible structural degradation. In this work, we report a post-synthesis strategy to fabricate photochromic microparticles, where donor-acceptor Stenhouse adducts (DASAs) are applied as the photoresponsive molecules. Unlike direct loading, hydrostable precursors are loaded during the formation of polymeric microparticles, followed by synthesizing the DASAs inside the microparticles in a water-free environment. The photochromic microparticles are reversibly switched between colored and colorless states under the control of visible light irradiation and heat, while also exhibiting improved stability under hygrothermal conditions. Further applications of the photochromic microparticles as smart additives are demonstrated for controlling color-switching of bulk materials and rewritable photopatterning on surfaces. The post-synthesis approach is envisioned as a general strategy to fabricate microparticles with water-sensitive functional molecules.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"37 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Post-Synthesis of Donor-Acceptor Stenhouse Adducts into Photochromic Microparticles.\",\"authors\":\"Yinghao Ji,Fanxi Sun,Gaolu Zhu,Bo Han,Yuxuan Zhao,Daisheng Yang,Xu Deng,Longquan Chen,Yonghao Zheng,Chen Wei,Dongsheng Wang\",\"doi\":\"10.1021/acsami.5c04468\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Encapsulating photoresponsive molecules into polymers is an effective strategy to achieve fast and efficient photochromism in the solid state. Water is often used as the dispersion phase for the formation of polymeric microparticles; however, it reacts with the photoresponsive molecules and induces irreversible structural degradation. In this work, we report a post-synthesis strategy to fabricate photochromic microparticles, where donor-acceptor Stenhouse adducts (DASAs) are applied as the photoresponsive molecules. Unlike direct loading, hydrostable precursors are loaded during the formation of polymeric microparticles, followed by synthesizing the DASAs inside the microparticles in a water-free environment. The photochromic microparticles are reversibly switched between colored and colorless states under the control of visible light irradiation and heat, while also exhibiting improved stability under hygrothermal conditions. Further applications of the photochromic microparticles as smart additives are demonstrated for controlling color-switching of bulk materials and rewritable photopatterning on surfaces. The post-synthesis approach is envisioned as a general strategy to fabricate microparticles with water-sensitive functional molecules.\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"37 1\",\"pages\":\"\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-05-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acsami.5c04468\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.5c04468","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Post-Synthesis of Donor-Acceptor Stenhouse Adducts into Photochromic Microparticles.
Encapsulating photoresponsive molecules into polymers is an effective strategy to achieve fast and efficient photochromism in the solid state. Water is often used as the dispersion phase for the formation of polymeric microparticles; however, it reacts with the photoresponsive molecules and induces irreversible structural degradation. In this work, we report a post-synthesis strategy to fabricate photochromic microparticles, where donor-acceptor Stenhouse adducts (DASAs) are applied as the photoresponsive molecules. Unlike direct loading, hydrostable precursors are loaded during the formation of polymeric microparticles, followed by synthesizing the DASAs inside the microparticles in a water-free environment. The photochromic microparticles are reversibly switched between colored and colorless states under the control of visible light irradiation and heat, while also exhibiting improved stability under hygrothermal conditions. Further applications of the photochromic microparticles as smart additives are demonstrated for controlling color-switching of bulk materials and rewritable photopatterning on surfaces. The post-synthesis approach is envisioned as a general strategy to fabricate microparticles with water-sensitive functional molecules.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.