{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,14]],"date-time":"2026-09-14T18:46:22Z","timestamp":1789411582216,"version":"build-2803163510"},"reference-count":160,"publisher":"MDPI AG","issue":"20","license":[{"start":{"date-parts":[[2019,10,16]],"date-time":"2019-10-16T00:00:00Z","timestamp":1571184000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["21804085"],"award-info":[{"award-number":["21804085"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Molecules"],"abstract":"<jats:p>Thiophenol (PhSH) belongs to a class of highly reactive and toxic aromatic thiols with widespread applications in the chemical industry for preparing pesticides, polymers, and pharmaceuticals. In this review, we comprehensively summarize recent progress in the development of fluorescent probes for detecting and imaging PhSH. These probes are classified according to recognition moieties and are detailed on the basis of their structures and sensing performances. In addition, prospects for future research are also discussed.<\/jats:p>","DOI":"10.3390\/molecules24203716","type":"journal-article","created":{"date-parts":[[2019,10,17]],"date-time":"2019-10-17T04:46:06Z","timestamp":1571287566000},"page":"3716","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":39,"title":["Recent Progress in the Development of Fluorescent Probes for Thiophenol"],"prefix":"10.3390","volume":"24","author":[{"given":"Yuanqiang","family":"Hao","sequence":"first","affiliation":[{"name":"Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engineering, Henan Joint International Research Laboratory of Chemo\/Biosensing and Early Diagnosis of Major Diseases, Shangqiu Normal University, Shangqiu 476000, China"},{"name":"Key Laboratory of Theoretical Organic Chemistry and Function Molecule of Ministry of Education, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qianye","family":"Yin","sequence":"additional","affiliation":[{"name":"Key Laboratory of Theoretical Organic Chemistry and Function Molecule of Ministry of Education, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yintang","family":"Zhang","sequence":"additional","affiliation":[{"name":"Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engineering, Henan Joint International Research Laboratory of Chemo\/Biosensing and Early Diagnosis of Major Diseases, Shangqiu Normal University, Shangqiu 476000, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maotian","family":"Xu","sequence":"additional","affiliation":[{"name":"Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engineering, Henan Joint International Research Laboratory of Chemo\/Biosensing and Early Diagnosis of Major Diseases, Shangqiu Normal University, Shangqiu 476000, China"},{"name":"College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450001, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5509-2684","authenticated-orcid":false,"given":"Shu","family":"Chen","sequence":"additional","affiliation":[{"name":"Key Laboratory of Theoretical Organic Chemistry and Function Molecule of Ministry of Education, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2019,10,16]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"9955","DOI":"10.1016\/j.polymer.2005.07.058","article-title":"A theoretical investigation on the electronic and optical properties of \u03c0-conjugated copolymers with an efficient electron-accepting unit bithieno [3,2-b:2\u20323\u2032-e]pyridine","volume":"46","author":"Yang","year":"2005","journal-title":"Polymer"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"3917","DOI":"10.1016\/j.tet.2019.06.010","article-title":"Improved synthesis of the thiophenol precursor N-(4-chloro-3-mercaptophenyl)picolinamide for making the mGluR4 PET ligands","volume":"75","author":"Wang","year":"2019","journal-title":"Tetrahedron"},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"5443","DOI":"10.1021\/acscatal.8b00906","article-title":"Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones","volume":"8","author":"Maddox","year":"2018","journal-title":"ACS Catal."},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1080\/03601238909372654","article-title":"Toxicological properties of thio- and alkylphenols causing flavor tainting in fish from the upper Wisconsin River","volume":"24","author":"Hell","year":"1989","journal-title":"J. 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