{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,18]],"date-time":"2026-06-18T15:02:47Z","timestamp":1781794967366,"version":"3.54.5"},"reference-count":39,"publisher":"Elsevier BV","issue":"11","license":[{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,10,23]],"date-time":"2023-10-23T00:00:00Z","timestamp":1698019200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100006529","name":"Race and Difference Initiative, Emory University","doi-asserted-by":"publisher","award":["127324"],"award-info":[{"award-number":["127324"]}],"id":[{"id":"10.13039\/100006529","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100018987","name":"Ministerul Cercet\u0103rii, Inov\u0103rii \u015fi Digitaliz\u0103rii","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100018987","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100021028","name":"Universitatea Alexandru Ioan Cuza din Ia\u0219i","doi-asserted-by":"publisher","award":["GI-UAIC-2021-10"],"award-info":[{"award-number":["GI-UAIC-2021-10"]}],"id":[{"id":"10.13039\/100021028","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["cell.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Heliyon"],"published-print":{"date-parts":[[2023,11]]},"DOI":"10.1016\/j.heliyon.2023.e21518","type":"journal-article","created":{"date-parts":[[2023,11,3]],"date-time":"2023-11-03T16:19:10Z","timestamp":1699028350000},"page":"e21518","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity"],"prefix":"10.1016","volume":"9","author":[{"given":"Dumitrela","family":"Diaconu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Violeta","family":"Mangalagiu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Simona","family":"Dunca","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dorina","family":"Amariucai-Mantu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vasilichia","family":"Antoci","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tiberiu","family":"Roman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4632-5076","authenticated-orcid":false,"given":"Ionel I.","family":"Mangalagiu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.heliyon.2023.e21518_bib1","series-title":"Organic Sonochemistry, Challenges and Perspectives for the 21st Century","author":"L\u00e9veque","year":"2018"},{"key":"10.1016\/j.heliyon.2023.e21518_bib2","series-title":"Handbook on Applications of Ultrasound: Sonochemistry for Sustainability","author":"Dong","year":"2012"},{"key":"10.1016\/j.heliyon.2023.e21518_bib3","series-title":"Practical Sonochemistry: Power Ultrasound Uses and Applications","author":"Mason","year":"2002"},{"key":"10.1016\/j.heliyon.2023.e21518_bib4","series-title":"Synthetic Organic Sonochemistry","author":"Luche","year":"1998"},{"key":"10.1016\/j.heliyon.2023.e21518_bib5","doi-asserted-by":"crossref","first-page":"2129","DOI":"10.1016\/j.tetlet.2006.01.127","article-title":"Rapid and efficient synthesis of 2-imidazolines and bis-imidazolines under ultrasonic irradiation","volume":"47","author":"Mirkhani","year":"2006","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.heliyon.2023.e21518_bib6","doi-asserted-by":"crossref","first-page":"476","DOI":"10.1016\/j.ultsonch.2006.10.008","article-title":"Sonochemistry and the environment - providing a \"green\" link between chemistry, physics and engineering","volume":"14","author":"Mason","year":"2007","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib7","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1016\/j.ultsonch.2004.12.005","article-title":"Efficient and selective hydrocarbon oxidation with sodium periodate under ultrasonic irradiation catalyzed by polystyrene-bound Mn (TPyP)","volume":"13","author":"Tangestaninejad","year":"2006","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib8","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/j.ultsonch.2015.04.030","article-title":"Sono-bromination of aromatic compounds based on the ultrasonic advanced oxidation processes","volume":"27","author":"Fujita","year":"2015","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib9","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1016\/j.ultsonch.2015.07.024","article-title":"Ultrasound and green chemistry \u2013 further comments","volume":"28","author":"Cintas","year":"2016","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib10","doi-asserted-by":"crossref","first-page":"609","DOI":"10.1016\/j.tet.2016.12.014","article-title":"Sonochemistry in non-conventional, green solvents or solvent-free reactions","volume":"73","author":"Lupacchini","year":"2017","journal-title":"Tetrahedron"},{"key":"10.1016\/j.heliyon.2023.e21518_bib11","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1016\/j.ultsonch.2017.03.029","article-title":"How sonochemistry contributes to green chemistry?","volume":"40","author":"Chatel","year":"2018","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib12","doi-asserted-by":"crossref","first-page":"802","DOI":"10.1016\/j.ultsonch.2013.09.012","article-title":"Ultrasound and microwave assisted synthesis of dihydroxyacetophenone derivatives with or without 1,2-diazine skeleton","volume":"21","author":"Zbancioc","year":"2014","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib13","doi-asserted-by":"crossref","first-page":"476","DOI":"10.2174\/15734064113096660070","article-title":"Synthesis and in vitro analysis of novel dihydroxyacetophenone derivatives with antimicrobial and antitumor activities","volume":"10","author":"Zbancioc","year":"2014","journal-title":"Med. Chem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib14","doi-asserted-by":"crossref","first-page":"999","DOI":"10.1016\/j.ultsonch.2012.02.012","article-title":"Ultrasound and microwave assisted synthesis of isoindolo-1,2-diazine: a comparative study","volume":"19","author":"Bejan","year":"2012","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib15","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1016\/j.ultsonch.2011.08.001","article-title":"An efficient and selective way to new highly functionalized coronands or spiro derivatives using ultrasonic irradiation","volume":"19","author":"Zbancioc","year":"2012","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib16","doi-asserted-by":"crossref","first-page":"5164","DOI":"10.1016\/j.ejmech.2010.08.029","article-title":"Synthesis and antituberculosis activity of some new pyridazine derivatives. Part II","volume":"45","author":"Mantu","year":"2010","journal-title":"Eur. J. Med. Chem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib17","doi-asserted-by":"crossref","first-page":"312","DOI":"10.1016\/j.ultsonch.2008.10.012","article-title":"Ultrasounds assisted reactions of steroid analogous of anticipated biological activities","volume":"16","author":"Bejan","year":"2009","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib18","doi-asserted-by":"crossref","first-page":"452","DOI":"10.1016\/j.ultsonch.2008.11.012","article-title":"A facile synthesis of pyridazinone derivatives under ultrasonic irradiation","volume":"16","author":"Mantu","year":"2009","journal-title":"Ultrason. Sonochem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib19","series-title":"The Organic Chemistry of Drug Design and Drug Action","author":"Silverman","year":"2014"},{"key":"10.1016\/j.heliyon.2023.e21518_bib20","doi-asserted-by":"crossref","first-page":"2026","DOI":"10.3390\/pharmaceutics14102026","article-title":"Hybrid azine derivatives: a useful approach for antimicrobial therapy","volume":"14","author":"Amariucai-Mantu","year":"2022","journal-title":"Pharmaceutics"},{"key":"10.1016\/j.heliyon.2023.e21518_bib21","doi-asserted-by":"crossref","DOI":"10.1038\/s41598-022-21435-6","article-title":"Quinoline - imidazole\/benzimidazole derivatives as dual-\/multi- targeting hybrids inhibitors with anticancer and antimicrobial activity","volume":"12","author":"Diaconu","year":"2022","journal-title":"Sci. Rep."},{"key":"10.1016\/j.heliyon.2023.e21518_bib22","doi-asserted-by":"crossref","first-page":"625","DOI":"10.1007\/s00044-022-02866-2","article-title":"Design, synthesis and biological evaluation of 8-aminoquinoline-1,2,3-triazole hybrid derivatives as potential antimicrobial agents","volume":"31","author":"Albayrak","year":"2022","journal-title":"Med. Chem. Res."},{"key":"10.1016\/j.heliyon.2023.e21518_bib23","doi-asserted-by":"crossref","DOI":"10.1016\/j.molstruc.2022.133634","article-title":"A review: structure-activity relationship and antibacterial activities of quinoline based hybrids","volume":"1268","author":"Patel","year":"2022","journal-title":"J. Mol. Struct."},{"key":"10.1016\/j.heliyon.2023.e21518_bib24","doi-asserted-by":"crossref","first-page":"1757","DOI":"10.2174\/1381612826666201006125644","article-title":"Quinoline-based compounds as key candidates to tackle drug discovery programs of microbicidal agents","volume":"27","author":"da Gama","year":"2021","journal-title":"Curr. Pharmaceut. Des."},{"key":"10.1016\/j.heliyon.2023.e21518_bib25","doi-asserted-by":"crossref","first-page":"917","DOI":"10.1016\/j.ejmech.2018.08.040","article-title":"A review on diverse heterocyclic compounds as the privileged scaffolds in antimalarial drug discovery","volume":"158","author":"Kalaria","year":"2018","journal-title":"Eur. J. Med. Chem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib26","doi-asserted-by":"crossref","first-page":"2946","DOI":"10.3390\/molecules25122946","article-title":"Hybrid quinoline-sulfonamide complexes (M2+) derivatives with antimicrobial activity","volume":"25","author":"Diaconu","year":"2020","journal-title":"Molecules"},{"key":"10.1016\/j.heliyon.2023.e21518_bib27","doi-asserted-by":"crossref","first-page":"2052","DOI":"10.2174\/1389557520666200905125738","article-title":"From antibacterial to antitumour agents: a brief review on the chemical and medicinal aspects of sulfonamides","volume":"20","author":"Azevedo-Barbosa","year":"2020","journal-title":"Mini-Rev. Med. Chem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib28","author":"Who"},{"key":"10.1016\/j.heliyon.2023.e21518_bib29","doi-asserted-by":"crossref","first-page":"576e584","DOI":"10.1016\/j.molstruc.2017.08.022","article-title":"Distorted square-antiprism geometry of new zirconium (IV) Schiff base complexes: synthesis, spectral characterization, crystal structure and investigation of biological properties","volume":"1149","author":"Sahraei","year":"2017","journal-title":"J. Mol. Struct."},{"key":"10.1016\/j.heliyon.2023.e21518_bib30","doi-asserted-by":"crossref","first-page":"483","DOI":"10.1007\/s11243-017-0152-x","article-title":"Synthesis, characterization, crystal structures and biological activities of eight-coordinate zirconium(IV) Schiff base complexes","volume":"42","author":"Sahraei","year":"2017","journal-title":"Transit. Met. Chem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib31","doi-asserted-by":"crossref","first-page":"335","DOI":"10.3390\/ph14040335","article-title":"Benzoquinoline derivatives: a straightforward and efficient route to antibacterial and antifungal agents","volume":"14","author":"Antoci","year":"2021","journal-title":"Pharmaceuticals"},{"key":"10.1016\/j.heliyon.2023.e21518_bib32","first-page":"3","article-title":"Metal complexes in medicine and pharmacy: the past and the present II","volume":"69","author":"Habala","year":"2020","journal-title":"CeskaSlov. Farm."},{"key":"10.1016\/j.heliyon.2023.e21518_bib33","doi-asserted-by":"crossref","first-page":"1729","DOI":"10.2174\/0929867325666171206102501","article-title":"Metallopharmaceuticals in therapy - a new horizon for scientific research","volume":"25","author":"Chylewska","year":"2018","journal-title":"Curr. Med. Chem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib34","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1080\/14756366.2016.1187143","article-title":"A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents","volume":"31","author":"A Diaz","year":"2016","journal-title":"J. Enz. Inhib.Med. Chem."},{"key":"10.1016\/j.heliyon.2023.e21518_bib35","doi-asserted-by":"crossref","first-page":"679","DOI":"10.2174\/157018010792929586","article-title":"In vitro antiprotozoal evaluation of zinc and copper complexes based on sulfonamides containing 8-aminoquinoline ligands","volume":"7","author":"Da Silva","year":"2010","journal-title":"Lett. Drug Des. Discov."},{"key":"10.1016\/j.heliyon.2023.e21518_bib36","doi-asserted-by":"crossref","first-page":"1161","DOI":"10.1590\/S0100-40422008000500044","article-title":"Synthesis, structure and physicochemical properties of zinc and copper complexes based on sulfonamides containing 8-aminoquinoline ligands","volume":"31","author":"Da Silva","year":"2008","journal-title":"Quim. Nova"},{"key":"10.1016\/j.heliyon.2023.e21518_bib37","first-page":"1","article-title":"Coordination behavior of Ni 2+, Cu 2+, and Zn2+ in tetrahedral 1-methylimidazole complexes: a DFT\/CSD study","volume":"157969","author":"Tetteh","year":"2018","journal-title":"Bioinorgan. Chem. Appl."},{"key":"10.1016\/j.heliyon.2023.e21518_bib38","series-title":"Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically; Approved Standard","year":"2018"},{"key":"10.1016\/j.heliyon.2023.e21518_bib39","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1128\/AAC.01760-18","article-title":"Effects of microplate type and broth additives on microdilution MIC susceptibility assays","volume":"63","author":"Kavanagh","year":"2019","journal-title":"Antimicrob. Agents Chemother."}],"container-title":["Heliyon"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2405844023087261?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2405844023087261?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,5,15]],"date-time":"2026-05-15T22:28:27Z","timestamp":1778884107000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2405844023087261"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,11]]},"references-count":39,"journal-issue":{"issue":"11","published-print":{"date-parts":[[2023,11]]}},"alternative-id":["S2405844023087261"],"URL":"https:\/\/doi.org\/10.1016\/j.heliyon.2023.e21518","relation":{},"ISSN":["2405-8440"],"issn-type":[{"value":"2405-8440","type":"print"}],"subject":[],"published":{"date-parts":[[2023,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity","name":"articletitle","label":"Article Title"},{"value":"Heliyon","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.heliyon.2023.e21518","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 The Authors. Published by Elsevier Ltd.","name":"copyright","label":"Copyright"}],"article-number":"e21518"}}