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Hg(2+) -induced in situ generated radical cation of (S)-BINOL-based polymer for highly enantioselective recognition of phenylalaninol
Phenylalaninol enantiomers are one of the most important chiral compounds due to its presence in biologically active molecules and pharmaceutical products. In this paper, a novel chiral fluorescence polymer sensor incorporating (S)-BINOL and oligomeric aniline via a nucleophilic addition-elimination...
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Published in: | Macromolecular rapid communications. 2014-08, Vol.35 (16), p.1443-1449 |
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creator | Jiao, Jiemin Li, Fei Zhang, Shuwei Quan, Yiwu Zheng, Wenhua Cheng, Yixiang Zhu, Chengjian |
description | Phenylalaninol enantiomers are one of the most important chiral compounds due to its presence in biologically active molecules and pharmaceutical products. In this paper, a novel chiral fluorescence polymer sensor incorporating (S)-BINOL and oligomeric aniline via a nucleophilic addition-elimination reaction is designed and synthesized. Polymer sensor exhibits "turn-off" fluorescence quenching response upon the addition of Hg(2+) , and "turn-on" moderate fluorescence enhancement behavior towards phenylalaninol enantiomers. Meanwhile, this kind of (S)-BINOL-based polymer sensor can exhibit highly selective enantioselective recognition response towards (L)-phenylalaninol upon the addition of Hg(2+) and the value of ef can reach as high as 5.4, which can be attributed to the formation of in situ generated radical cation arisen from oligomeric aniline moiety by Hg(2+) induction. |
doi_str_mv | 10.1002/marc.201400248 |
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In this paper, a novel chiral fluorescence polymer sensor incorporating (S)-BINOL and oligomeric aniline via a nucleophilic addition-elimination reaction is designed and synthesized. Polymer sensor exhibits "turn-off" fluorescence quenching response upon the addition of Hg(2+) , and "turn-on" moderate fluorescence enhancement behavior towards phenylalaninol enantiomers. Meanwhile, this kind of (S)-BINOL-based polymer sensor can exhibit highly selective enantioselective recognition response towards (L)-phenylalaninol upon the addition of Hg(2+) and the value of ef can reach as high as 5.4, which can be attributed to the formation of in situ generated radical cation arisen from oligomeric aniline moiety by Hg(2+) induction.</description><identifier>EISSN: 1521-3927</identifier><identifier>DOI: 10.1002/marc.201400248</identifier><identifier>PMID: 25048009</identifier><language>eng</language><publisher>Germany</publisher><subject>Cations - chemistry ; Fluorescent Dyes - chemistry ; Mercury - chemistry ; Naphthols - chemistry ; Phenylalanine - analogs & derivatives ; Phenylalanine - analysis ; Polymers - chemistry ; Spectrometry, Fluorescence ; Stereoisomerism</subject><ispartof>Macromolecular rapid communications., 2014-08, Vol.35 (16), p.1443-1449</ispartof><rights>2014 WILEY-VCH Verlag GmbH & Co. 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In this paper, a novel chiral fluorescence polymer sensor incorporating (S)-BINOL and oligomeric aniline via a nucleophilic addition-elimination reaction is designed and synthesized. Polymer sensor exhibits "turn-off" fluorescence quenching response upon the addition of Hg(2+) , and "turn-on" moderate fluorescence enhancement behavior towards phenylalaninol enantiomers. Meanwhile, this kind of (S)-BINOL-based polymer sensor can exhibit highly selective enantioselective recognition response towards (L)-phenylalaninol upon the addition of Hg(2+) and the value of ef can reach as high as 5.4, which can be attributed to the formation of in situ generated radical cation arisen from oligomeric aniline moiety by Hg(2+) induction.</description><subject>Cations - chemistry</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Mercury - chemistry</subject><subject>Naphthols - chemistry</subject><subject>Phenylalanine - analogs & derivatives</subject><subject>Phenylalanine - analysis</subject><subject>Polymers - chemistry</subject><subject>Spectrometry, Fluorescence</subject><subject>Stereoisomerism</subject><issn>1521-3927</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNo1kM9LwzAcxYMgbk6vHiXHDenMj6ZNjzrUDYY7qOeSpt90kTStTSv0D_D_tqA7Pd7jw-PxELqhZE0JYfe16vSaERpPJpZnaE4FoxHPWDpDlyF8EkJkTNgFmjFBYklINkc_22rJ7lY4sr4cNJTYehxsP-AKPHSqn5JOlVYrh7XqbeNxY_DybRU97l4P-6hQYSLaxo01dNg0HT7a6uhGDF75CQ_gQPf2G3AHuqm8PVW0R_CjU0556xt3hc6NcgGu_3WBPp6f3jfbaH942W0e9lFLRdZHnHOSmJhCJqBMeCwKkWZZog0jKVE6k4oKrUojRFECL7gsjEwKAJmawug04Qu0_Ottu-ZrgNDntQ0a3DQDmiHkVAjB4owKOaG3_-hQ1FDmbWenf8f8dB3_BYplb_I</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Jiao, Jiemin</creator><creator>Li, Fei</creator><creator>Zhang, Shuwei</creator><creator>Quan, Yiwu</creator><creator>Zheng, Wenhua</creator><creator>Cheng, Yixiang</creator><creator>Zhu, Chengjian</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201408</creationdate><title>Hg(2+) -induced in situ generated radical cation of (S)-BINOL-based polymer for highly enantioselective recognition of phenylalaninol</title><author>Jiao, Jiemin ; Li, Fei ; Zhang, Shuwei ; Quan, Yiwu ; Zheng, Wenhua ; Cheng, Yixiang ; Zhu, Chengjian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p159t-33306f41e95ed6345b57996cf2070ac98a15cadf55bde3b38bf86bee87fbfc763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Cations - chemistry</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Mercury - chemistry</topic><topic>Naphthols - chemistry</topic><topic>Phenylalanine - analogs & derivatives</topic><topic>Phenylalanine - analysis</topic><topic>Polymers - chemistry</topic><topic>Spectrometry, Fluorescence</topic><topic>Stereoisomerism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiao, Jiemin</creatorcontrib><creatorcontrib>Li, Fei</creatorcontrib><creatorcontrib>Zhang, Shuwei</creatorcontrib><creatorcontrib>Quan, Yiwu</creatorcontrib><creatorcontrib>Zheng, Wenhua</creatorcontrib><creatorcontrib>Cheng, Yixiang</creatorcontrib><creatorcontrib>Zhu, Chengjian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Macromolecular rapid communications.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiao, Jiemin</au><au>Li, Fei</au><au>Zhang, Shuwei</au><au>Quan, Yiwu</au><au>Zheng, Wenhua</au><au>Cheng, Yixiang</au><au>Zhu, Chengjian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hg(2+) -induced in situ generated radical cation of (S)-BINOL-based polymer for highly enantioselective recognition of phenylalaninol</atitle><jtitle>Macromolecular rapid communications.</jtitle><addtitle>Macromol Rapid Commun</addtitle><date>2014-08</date><risdate>2014</risdate><volume>35</volume><issue>16</issue><spage>1443</spage><epage>1449</epage><pages>1443-1449</pages><eissn>1521-3927</eissn><abstract>Phenylalaninol enantiomers are one of the most important chiral compounds due to its presence in biologically active molecules and pharmaceutical products. In this paper, a novel chiral fluorescence polymer sensor incorporating (S)-BINOL and oligomeric aniline via a nucleophilic addition-elimination reaction is designed and synthesized. Polymer sensor exhibits "turn-off" fluorescence quenching response upon the addition of Hg(2+) , and "turn-on" moderate fluorescence enhancement behavior towards phenylalaninol enantiomers. Meanwhile, this kind of (S)-BINOL-based polymer sensor can exhibit highly selective enantioselective recognition response towards (L)-phenylalaninol upon the addition of Hg(2+) and the value of ef can reach as high as 5.4, which can be attributed to the formation of in situ generated radical cation arisen from oligomeric aniline moiety by Hg(2+) induction.</abstract><cop>Germany</cop><pmid>25048009</pmid><doi>10.1002/marc.201400248</doi><tpages>7</tpages></addata></record> |
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subjects | Cations - chemistry Fluorescent Dyes - chemistry Mercury - chemistry Naphthols - chemistry Phenylalanine - analogs & derivatives Phenylalanine - analysis Polymers - chemistry Spectrometry, Fluorescence Stereoisomerism |
title | Hg(2+) -induced in situ generated radical cation of (S)-BINOL-based polymer for highly enantioselective recognition of phenylalaninol |
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