Xiaoni Zhao , Tao Liu , Xuwei Han , Fangjun Huo , Yongkang Yue , Caixia Yin
{"title":"光拉伸调制构建多种可激活的光功能染料","authors":"Xiaoni Zhao , Tao Liu , Xuwei Han , Fangjun Huo , Yongkang Yue , Caixia Yin","doi":"10.1016/j.dyepig.2025.112890","DOIUrl":null,"url":null,"abstract":"<div><div>A Phenoxazinone based fluorophore and its acylated derivatives were reported in this work. Interestingly, the present fluorescence modulation mechanisms failed to explain the acylation induced fluorescence activation in this series of dyes. Supported by exhaustive theoretical calculation and experimental validation, we proposed the bond photo-stretching as a molecular mechanism that modulated the abnormal photophysical property. Specifically, photo excitation of Phenoxazinone-NH<sub>2</sub> induced distinctly stretching of a C<img>C bond adjacent to the asymmetric amino group to quench the excited state energy via non-radiative transition. Upon acylation, however, the contribution of the nitrogen moiety to the HOMO and LUMO of the fluorophore reduced significantly which thus resulted a contraction of structural changes between the ground and excited states to enhance the radiative transition. The fluorophore in this work supports us to construct multiple biomolecules activable photo functional dyes with controllable photon to heat transformation.</div></div>","PeriodicalId":302,"journal":{"name":"Dyes and Pigments","volume":"241 ","pages":"Article 112890"},"PeriodicalIF":4.1000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photo-stretching modulation to construct multiple activable photo-functional dyes\",\"authors\":\"Xiaoni Zhao , Tao Liu , Xuwei Han , Fangjun Huo , Yongkang Yue , Caixia Yin\",\"doi\":\"10.1016/j.dyepig.2025.112890\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A Phenoxazinone based fluorophore and its acylated derivatives were reported in this work. Interestingly, the present fluorescence modulation mechanisms failed to explain the acylation induced fluorescence activation in this series of dyes. Supported by exhaustive theoretical calculation and experimental validation, we proposed the bond photo-stretching as a molecular mechanism that modulated the abnormal photophysical property. Specifically, photo excitation of Phenoxazinone-NH<sub>2</sub> induced distinctly stretching of a C<img>C bond adjacent to the asymmetric amino group to quench the excited state energy via non-radiative transition. Upon acylation, however, the contribution of the nitrogen moiety to the HOMO and LUMO of the fluorophore reduced significantly which thus resulted a contraction of structural changes between the ground and excited states to enhance the radiative transition. The fluorophore in this work supports us to construct multiple biomolecules activable photo functional dyes with controllable photon to heat transformation.</div></div>\",\"PeriodicalId\":302,\"journal\":{\"name\":\"Dyes and Pigments\",\"volume\":\"241 \",\"pages\":\"Article 112890\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dyes and Pigments\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0143720825002608\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dyes and Pigments","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0143720825002608","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Photo-stretching modulation to construct multiple activable photo-functional dyes
A Phenoxazinone based fluorophore and its acylated derivatives were reported in this work. Interestingly, the present fluorescence modulation mechanisms failed to explain the acylation induced fluorescence activation in this series of dyes. Supported by exhaustive theoretical calculation and experimental validation, we proposed the bond photo-stretching as a molecular mechanism that modulated the abnormal photophysical property. Specifically, photo excitation of Phenoxazinone-NH2 induced distinctly stretching of a CC bond adjacent to the asymmetric amino group to quench the excited state energy via non-radiative transition. Upon acylation, however, the contribution of the nitrogen moiety to the HOMO and LUMO of the fluorophore reduced significantly which thus resulted a contraction of structural changes between the ground and excited states to enhance the radiative transition. The fluorophore in this work supports us to construct multiple biomolecules activable photo functional dyes with controllable photon to heat transformation.
期刊介绍:
Dyes and Pigments covers the scientific and technical aspects of the chemistry and physics of dyes, pigments and their intermediates. Emphasis is placed on the properties of the colouring matters themselves rather than on their applications or the system in which they may be applied.
Thus the journal accepts research and review papers on the synthesis of dyes, pigments and intermediates, their physical or chemical properties, e.g. spectroscopic, surface, solution or solid state characteristics, the physical aspects of their preparation, e.g. precipitation, nucleation and growth, crystal formation, liquid crystalline characteristics, their photochemical, ecological or biological properties and the relationship between colour and chemical constitution. However, papers are considered which deal with the more fundamental aspects of colourant application and of the interactions of colourants with substrates or media.
The journal will interest a wide variety of workers in a range of disciplines whose work involves dyes, pigments and their intermediates, and provides a platform for investigators with common interests but diverse fields of activity such as cosmetics, reprographics, dye and pigment synthesis, medical research, polymers, etc.