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Spectroscopic properties of push-pull 2-(4-carboxyphenyl)-6-dimethylaminobenzothiazole derivatives in solution and the solid state
[Display omitted] •Push-pull benzothiazole derivatives were designed based on firefly oxyluciferin.•The derivatives show solvatochromic fluorescence with high quantum yields.•Solid state fluorescence of the derivatives were depended on the crystal structures. 6-Dimethylamino-2-phenylbenzothiazoles w...
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Published in: | Journal of photochemistry and photobiology. A, Chemistry. Chemistry., 2019-05, Vol.376, p.324-332 |
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container_title | Journal of photochemistry and photobiology. A, Chemistry. |
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creator | Takahashi, Yusuke Uehara, Takuya Matsuhashi, Chihiro Yamaji, Minoru Mutai, Toshiki Yoshikawa, Isao Houjou, Hirohiko Kitagawa, Kota Suenobu, Tomoyoshi Maki, Shojiro Hirano, Takashi |
description | [Display omitted]
•Push-pull benzothiazole derivatives were designed based on firefly oxyluciferin.•The derivatives show solvatochromic fluorescence with high quantum yields.•Solid state fluorescence of the derivatives were depended on the crystal structures.
6-Dimethylamino-2-phenylbenzothiazoles with a carboxy, ester and amide substituent on the 2-phenyl group were prepared as a series of the push-pull benzothiazoles, and their spectroscopic and photophysical properties in solutions were investigated. The derivatives showed solvatochromic fluorescence with quantum yields over 0.68 in various organic solvents similar to the core fluorophore structure. The color variation ranges in fluorescence solvatochromism of the derivatives were wider than that of the original compound having the core structure, 6-dimethylamino-2-phenylbenzothiazole. It was also found that the derivatives together with the original compound show solid state fluorescence depending on their crystal structures. In particular, an ester derivative with a protected serine has a reasonable crystal packing leading to increase in fluorescence efficiency. The results of the present study provide a guide to design push-pull 2-phenylbenzothiazoles exhibiting fluorescence in solution and the solid state. |
doi_str_mv | 10.1016/j.jphotochem.2019.03.021 |
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•Push-pull benzothiazole derivatives were designed based on firefly oxyluciferin.•The derivatives show solvatochromic fluorescence with high quantum yields.•Solid state fluorescence of the derivatives were depended on the crystal structures.
6-Dimethylamino-2-phenylbenzothiazoles with a carboxy, ester and amide substituent on the 2-phenyl group were prepared as a series of the push-pull benzothiazoles, and their spectroscopic and photophysical properties in solutions were investigated. The derivatives showed solvatochromic fluorescence with quantum yields over 0.68 in various organic solvents similar to the core fluorophore structure. The color variation ranges in fluorescence solvatochromism of the derivatives were wider than that of the original compound having the core structure, 6-dimethylamino-2-phenylbenzothiazole. It was also found that the derivatives together with the original compound show solid state fluorescence depending on their crystal structures. In particular, an ester derivative with a protected serine has a reasonable crystal packing leading to increase in fluorescence efficiency. The results of the present study provide a guide to design push-pull 2-phenylbenzothiazoles exhibiting fluorescence in solution and the solid state.</description><identifier>ISSN: 1010-6030</identifier><identifier>EISSN: 1873-2666</identifier><identifier>DOI: 10.1016/j.jphotochem.2019.03.021</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Benzothiazole ; Crystal structure ; Derivatives ; Firefly oxyluciferin ; Fluorescence ; Fluorescence solvatochromism ; Organic solvents ; Serine ; Solid state ; Solid state fluorescence ; Solvents ; Spectroscopy ; Substituent effect</subject><ispartof>Journal of photochemistry and photobiology. A, Chemistry., 2019-05, Vol.376, p.324-332</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright Elsevier BV May 1, 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-83c9313cc86892a65b23c14eed90f6bfeb5075797b37f3b11189de26376ca04a3</citedby><cites>FETCH-LOGICAL-c412t-83c9313cc86892a65b23c14eed90f6bfeb5075797b37f3b11189de26376ca04a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Takahashi, Yusuke</creatorcontrib><creatorcontrib>Uehara, Takuya</creatorcontrib><creatorcontrib>Matsuhashi, Chihiro</creatorcontrib><creatorcontrib>Yamaji, Minoru</creatorcontrib><creatorcontrib>Mutai, Toshiki</creatorcontrib><creatorcontrib>Yoshikawa, Isao</creatorcontrib><creatorcontrib>Houjou, Hirohiko</creatorcontrib><creatorcontrib>Kitagawa, Kota</creatorcontrib><creatorcontrib>Suenobu, Tomoyoshi</creatorcontrib><creatorcontrib>Maki, Shojiro</creatorcontrib><creatorcontrib>Hirano, Takashi</creatorcontrib><title>Spectroscopic properties of push-pull 2-(4-carboxyphenyl)-6-dimethylaminobenzothiazole derivatives in solution and the solid state</title><title>Journal of photochemistry and photobiology. A, Chemistry.</title><description>[Display omitted]
•Push-pull benzothiazole derivatives were designed based on firefly oxyluciferin.•The derivatives show solvatochromic fluorescence with high quantum yields.•Solid state fluorescence of the derivatives were depended on the crystal structures.
6-Dimethylamino-2-phenylbenzothiazoles with a carboxy, ester and amide substituent on the 2-phenyl group were prepared as a series of the push-pull benzothiazoles, and their spectroscopic and photophysical properties in solutions were investigated. The derivatives showed solvatochromic fluorescence with quantum yields over 0.68 in various organic solvents similar to the core fluorophore structure. The color variation ranges in fluorescence solvatochromism of the derivatives were wider than that of the original compound having the core structure, 6-dimethylamino-2-phenylbenzothiazole. It was also found that the derivatives together with the original compound show solid state fluorescence depending on their crystal structures. In particular, an ester derivative with a protected serine has a reasonable crystal packing leading to increase in fluorescence efficiency. The results of the present study provide a guide to design push-pull 2-phenylbenzothiazoles exhibiting fluorescence in solution and the solid state.</description><subject>Benzothiazole</subject><subject>Crystal structure</subject><subject>Derivatives</subject><subject>Firefly oxyluciferin</subject><subject>Fluorescence</subject><subject>Fluorescence solvatochromism</subject><subject>Organic solvents</subject><subject>Serine</subject><subject>Solid state</subject><subject>Solid state fluorescence</subject><subject>Solvents</subject><subject>Spectroscopy</subject><subject>Substituent effect</subject><issn>1010-6030</issn><issn>1873-2666</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkE9r3DAQxU1JoUna7yDoJT3IGf1Z2T62oWkDgR6SnoUsj7GM11Ikeenm2E9eLVvosacZhvfe8H5VRRjUDJi6nes5TD57O-G-5sC6GkQNnL2pLlnbCMqVUhdlBwZUgYB31VVKMwBIKdll9fspoM3RJ-uDsyREHzBmh4n4kYQtTTRsy0I4vZHUmtj7X8cw4XpcPlFFB7fHPB0Xs3er73F99Xly5tUvSAaM7mCyO5Qkt5Lkly07vxKzDiRPeDq4gaRsMr6v3o5mSfjh77yuft5_fb77Th9_fHu4-_xIrWQ801bYTjBhbavajhu167mwTCIOHYyqH7HfQbNruqYXzSh6xljbDciVaJQ1II24rj6ec0vJlw1T1rPf4lpeas45a1ohd7Ko2rPKFigp4qhDdHsTj5qBPhHXs_5HXJ-IaxC6EC_WL2crlhYHh1En63C1OLhYIOvBu_-H_AEatZHY</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Takahashi, Yusuke</creator><creator>Uehara, Takuya</creator><creator>Matsuhashi, Chihiro</creator><creator>Yamaji, Minoru</creator><creator>Mutai, Toshiki</creator><creator>Yoshikawa, Isao</creator><creator>Houjou, Hirohiko</creator><creator>Kitagawa, Kota</creator><creator>Suenobu, Tomoyoshi</creator><creator>Maki, Shojiro</creator><creator>Hirano, Takashi</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>20190501</creationdate><title>Spectroscopic properties of push-pull 2-(4-carboxyphenyl)-6-dimethylaminobenzothiazole derivatives in solution and the solid state</title><author>Takahashi, Yusuke ; Uehara, Takuya ; Matsuhashi, Chihiro ; Yamaji, Minoru ; Mutai, Toshiki ; Yoshikawa, Isao ; Houjou, Hirohiko ; Kitagawa, Kota ; Suenobu, Tomoyoshi ; Maki, Shojiro ; Hirano, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-83c9313cc86892a65b23c14eed90f6bfeb5075797b37f3b11189de26376ca04a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Benzothiazole</topic><topic>Crystal structure</topic><topic>Derivatives</topic><topic>Firefly oxyluciferin</topic><topic>Fluorescence</topic><topic>Fluorescence solvatochromism</topic><topic>Organic solvents</topic><topic>Serine</topic><topic>Solid state</topic><topic>Solid state fluorescence</topic><topic>Solvents</topic><topic>Spectroscopy</topic><topic>Substituent effect</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takahashi, Yusuke</creatorcontrib><creatorcontrib>Uehara, Takuya</creatorcontrib><creatorcontrib>Matsuhashi, Chihiro</creatorcontrib><creatorcontrib>Yamaji, Minoru</creatorcontrib><creatorcontrib>Mutai, Toshiki</creatorcontrib><creatorcontrib>Yoshikawa, Isao</creatorcontrib><creatorcontrib>Houjou, Hirohiko</creatorcontrib><creatorcontrib>Kitagawa, Kota</creatorcontrib><creatorcontrib>Suenobu, Tomoyoshi</creatorcontrib><creatorcontrib>Maki, Shojiro</creatorcontrib><creatorcontrib>Hirano, Takashi</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of photochemistry and photobiology. A, Chemistry.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takahashi, Yusuke</au><au>Uehara, Takuya</au><au>Matsuhashi, Chihiro</au><au>Yamaji, Minoru</au><au>Mutai, Toshiki</au><au>Yoshikawa, Isao</au><au>Houjou, Hirohiko</au><au>Kitagawa, Kota</au><au>Suenobu, Tomoyoshi</au><au>Maki, Shojiro</au><au>Hirano, Takashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spectroscopic properties of push-pull 2-(4-carboxyphenyl)-6-dimethylaminobenzothiazole derivatives in solution and the solid state</atitle><jtitle>Journal of photochemistry and photobiology. A, Chemistry.</jtitle><date>2019-05-01</date><risdate>2019</risdate><volume>376</volume><spage>324</spage><epage>332</epage><pages>324-332</pages><issn>1010-6030</issn><eissn>1873-2666</eissn><abstract>[Display omitted]
•Push-pull benzothiazole derivatives were designed based on firefly oxyluciferin.•The derivatives show solvatochromic fluorescence with high quantum yields.•Solid state fluorescence of the derivatives were depended on the crystal structures.
6-Dimethylamino-2-phenylbenzothiazoles with a carboxy, ester and amide substituent on the 2-phenyl group were prepared as a series of the push-pull benzothiazoles, and their spectroscopic and photophysical properties in solutions were investigated. The derivatives showed solvatochromic fluorescence with quantum yields over 0.68 in various organic solvents similar to the core fluorophore structure. The color variation ranges in fluorescence solvatochromism of the derivatives were wider than that of the original compound having the core structure, 6-dimethylamino-2-phenylbenzothiazole. It was also found that the derivatives together with the original compound show solid state fluorescence depending on their crystal structures. In particular, an ester derivative with a protected serine has a reasonable crystal packing leading to increase in fluorescence efficiency. The results of the present study provide a guide to design push-pull 2-phenylbenzothiazoles exhibiting fluorescence in solution and the solid state.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jphotochem.2019.03.021</doi><tpages>9</tpages></addata></record> |
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subjects | Benzothiazole Crystal structure Derivatives Firefly oxyluciferin Fluorescence Fluorescence solvatochromism Organic solvents Serine Solid state Solid state fluorescence Solvents Spectroscopy Substituent effect |
title | Spectroscopic properties of push-pull 2-(4-carboxyphenyl)-6-dimethylaminobenzothiazole derivatives in solution and the solid state |
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