Xingda Zhang, Tianya Zhang, Yanjun Zhao, Liming Lin, Qingbing Xia, Lijuan Bu, Ruiyang Ma, Zhimin Ma, Mingxing Chen, Yan Guan and Zhiyong Ma*,
{"title":"基于给体-受体结构的苯并咪唑衍生物的温度响应磷光精确激发态工程。","authors":"Xingda Zhang, Tianya Zhang, Yanjun Zhao, Liming Lin, Qingbing Xia, Lijuan Bu, Ruiyang Ma, Zhimin Ma, Mingxing Chen, Yan Guan and Zhiyong Ma*, ","doi":"10.1021/acsami.5c13317","DOIUrl":null,"url":null,"abstract":"<p >Herein, we report precise excited-state engineering in benzimidazole (NBd) derivatives via a donor–acceptor (D–A) architecture for organic temperature-responsive phosphorescence (RTP). Four NBd derivatives (1-NBdCN, 1-NBdBrCN, 2-NBdCN, and 2-NBdBrCN) with an electron acceptor at position 1 and position 2 were designed and synthesized. The position of the electron acceptor enables 1-NBdCN and 1-NBdBrCN with temperature-responsive phosphorescence and endows 2-NBdCN and 2-NBdBrCN with red-shifted phosphorescence, showing a remarkable site effect. First, phosphorescence properties of the four NBd derivatives were studied in solution at 77 K. 1-NBdCN and 1-NBdBrCN give out yellow afterglow in toluene solution but bluish-green afterglow in ethanol solution, displaying solvent-dependent double phosphorescence components. 2-NBdCN and 2-NBdBrCN emit orange afterglow both in toluene solution and in ethanol solution, suggesting position 2 leads to a red shift of phosphorescence. Second, copolymerized methyl methacrylate/acrylic acid copolymer (MA/AA) films of the four NBd derivatives all demonstrate RTP. 2-NBdCN and 2-NBdBrCN kept the orange afterglow whether at room temperature or at 77 K. However, 1-NBdCN and 1-NBdBrCN exhibit distinct temperature-responsive phosphorescence color change from bluish green to yellow with increasing temperature, indicating temperature-dependent expression of double phosphorescence components. TD-DFT and SOC results reveal that 1-NBdCN and 1-NBdBrCN have two phosphorescence pathways for triplet excitons from T<sub>1</sub> and T<sub>2</sub> due to their sensitive molecular conformations. Therefore, the double phosphorescence components of 1-NBdCN and 1-NBdBrCN arise from T<sub>1</sub> and T<sub>2</sub>, which are greatly affected by solvent polarity and temperature. This study gives a deep insight into the site effects of electron acceptors on RTP and paves a way for intelligent organic phosphorescence materials.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 31","pages":"44783–44791"},"PeriodicalIF":8.2000,"publicationDate":"2025-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Precise Excited-State Engineering in Benzimidazole Derivatives via Donor–Acceptor Architecture for Organic Temperature-Responsive Phosphorescence\",\"authors\":\"Xingda Zhang, Tianya Zhang, Yanjun Zhao, Liming Lin, Qingbing Xia, Lijuan Bu, Ruiyang Ma, Zhimin Ma, Mingxing Chen, Yan Guan and Zhiyong Ma*, \",\"doi\":\"10.1021/acsami.5c13317\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Herein, we report precise excited-state engineering in benzimidazole (NBd) derivatives via a donor–acceptor (D–A) architecture for organic temperature-responsive phosphorescence (RTP). Four NBd derivatives (1-NBdCN, 1-NBdBrCN, 2-NBdCN, and 2-NBdBrCN) with an electron acceptor at position 1 and position 2 were designed and synthesized. The position of the electron acceptor enables 1-NBdCN and 1-NBdBrCN with temperature-responsive phosphorescence and endows 2-NBdCN and 2-NBdBrCN with red-shifted phosphorescence, showing a remarkable site effect. First, phosphorescence properties of the four NBd derivatives were studied in solution at 77 K. 1-NBdCN and 1-NBdBrCN give out yellow afterglow in toluene solution but bluish-green afterglow in ethanol solution, displaying solvent-dependent double phosphorescence components. 2-NBdCN and 2-NBdBrCN emit orange afterglow both in toluene solution and in ethanol solution, suggesting position 2 leads to a red shift of phosphorescence. Second, copolymerized methyl methacrylate/acrylic acid copolymer (MA/AA) films of the four NBd derivatives all demonstrate RTP. 2-NBdCN and 2-NBdBrCN kept the orange afterglow whether at room temperature or at 77 K. However, 1-NBdCN and 1-NBdBrCN exhibit distinct temperature-responsive phosphorescence color change from bluish green to yellow with increasing temperature, indicating temperature-dependent expression of double phosphorescence components. TD-DFT and SOC results reveal that 1-NBdCN and 1-NBdBrCN have two phosphorescence pathways for triplet excitons from T<sub>1</sub> and T<sub>2</sub> due to their sensitive molecular conformations. Therefore, the double phosphorescence components of 1-NBdCN and 1-NBdBrCN arise from T<sub>1</sub> and T<sub>2</sub>, which are greatly affected by solvent polarity and temperature. This study gives a deep insight into the site effects of electron acceptors on RTP and paves a way for intelligent organic phosphorescence materials.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"17 31\",\"pages\":\"44783–44791\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-07-27\",\"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://pubs.acs.org/doi/10.1021/acsami.5c13317\",\"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://pubs.acs.org/doi/10.1021/acsami.5c13317","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}
Precise Excited-State Engineering in Benzimidazole Derivatives via Donor–Acceptor Architecture for Organic Temperature-Responsive Phosphorescence
Herein, we report precise excited-state engineering in benzimidazole (NBd) derivatives via a donor–acceptor (D–A) architecture for organic temperature-responsive phosphorescence (RTP). Four NBd derivatives (1-NBdCN, 1-NBdBrCN, 2-NBdCN, and 2-NBdBrCN) with an electron acceptor at position 1 and position 2 were designed and synthesized. The position of the electron acceptor enables 1-NBdCN and 1-NBdBrCN with temperature-responsive phosphorescence and endows 2-NBdCN and 2-NBdBrCN with red-shifted phosphorescence, showing a remarkable site effect. First, phosphorescence properties of the four NBd derivatives were studied in solution at 77 K. 1-NBdCN and 1-NBdBrCN give out yellow afterglow in toluene solution but bluish-green afterglow in ethanol solution, displaying solvent-dependent double phosphorescence components. 2-NBdCN and 2-NBdBrCN emit orange afterglow both in toluene solution and in ethanol solution, suggesting position 2 leads to a red shift of phosphorescence. Second, copolymerized methyl methacrylate/acrylic acid copolymer (MA/AA) films of the four NBd derivatives all demonstrate RTP. 2-NBdCN and 2-NBdBrCN kept the orange afterglow whether at room temperature or at 77 K. However, 1-NBdCN and 1-NBdBrCN exhibit distinct temperature-responsive phosphorescence color change from bluish green to yellow with increasing temperature, indicating temperature-dependent expression of double phosphorescence components. TD-DFT and SOC results reveal that 1-NBdCN and 1-NBdBrCN have two phosphorescence pathways for triplet excitons from T1 and T2 due to their sensitive molecular conformations. Therefore, the double phosphorescence components of 1-NBdCN and 1-NBdBrCN arise from T1 and T2, which are greatly affected by solvent polarity and temperature. This study gives a deep insight into the site effects of electron acceptors on RTP and paves a way for intelligent organic phosphorescence materials.
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.