{"title":"4-硝基苯酚表面诱导共振位移的发现使酶促反应能够直接监测（ad . Sensor Res. 10/2025）","authors":"Ayano Nakamura, Yusuke Kato, Toshiharu Gokan, Kentaro Arai, Yoshimi Kanie, Osamu Kanie","doi":"10.1002/adsr.70069","DOIUrl":null,"url":null,"abstract":"<p><b>Raman Microscopy</b></p><p>The resonance structure of 4-nitrophenol undergoes a distinct change upon interaction with surface-modified porous silica, as revealed by Raman microscopy. The silica surface is functionalized with a complex mixture comprising covalently attached acetylated mannoside via a linker, precipitated <i>N</i>-acylurea, and urea. The quinone-type resonance form can be monitored in situ without the need for alkaline treatment. More details can be found in the Research Article by Osamu Kanie and co-workers (DOI: 10.1002/adsr.202500093).\n\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":100037,"journal":{"name":"Advanced Sensor Research","volume":"4 10","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://advanced.onlinelibrary.wiley.com/doi/epdf/10.1002/adsr.70069","citationCount":"0","resultStr":"{\"title\":\"Discovery of Surface-Induced Resonance Shift of 4-Nitrophenol Enabling Direct Monitoring of an Enzymatic Reaction (Adv. Sensor Res. 10/2025)\",\"authors\":\"Ayano Nakamura, Yusuke Kato, Toshiharu Gokan, Kentaro Arai, Yoshimi Kanie, Osamu Kanie\",\"doi\":\"10.1002/adsr.70069\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>Raman Microscopy</b></p><p>The resonance structure of 4-nitrophenol undergoes a distinct change upon interaction with surface-modified porous silica, as revealed by Raman microscopy. The silica surface is functionalized with a complex mixture comprising covalently attached acetylated mannoside via a linker, precipitated <i>N</i>-acylurea, and urea. The quinone-type resonance form can be monitored in situ without the need for alkaline treatment. More details can be found in the Research Article by Osamu Kanie and co-workers (DOI: 10.1002/adsr.202500093).\\n\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure></p>\",\"PeriodicalId\":100037,\"journal\":{\"name\":\"Advanced Sensor Research\",\"volume\":\"4 10\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://advanced.onlinelibrary.wiley.com/doi/epdf/10.1002/adsr.70069\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Sensor Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsr.70069\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Sensor Research","FirstCategoryId":"1085","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsr.70069","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Discovery of Surface-Induced Resonance Shift of 4-Nitrophenol Enabling Direct Monitoring of an Enzymatic Reaction (Adv. Sensor Res. 10/2025)
Raman Microscopy
The resonance structure of 4-nitrophenol undergoes a distinct change upon interaction with surface-modified porous silica, as revealed by Raman microscopy. The silica surface is functionalized with a complex mixture comprising covalently attached acetylated mannoside via a linker, precipitated N-acylurea, and urea. The quinone-type resonance form can be monitored in situ without the need for alkaline treatment. More details can be found in the Research Article by Osamu Kanie and co-workers (DOI: 10.1002/adsr.202500093).
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