{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,22]],"date-time":"2025-12-22T05:43:43Z","timestamp":1766382223025,"version":"build-2065373602"},"reference-count":36,"publisher":"MDPI AG","issue":"2","license":[{"start":{"date-parts":[[2024,1,22]],"date-time":"2024-01-22T00:00:00Z","timestamp":1705881600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Nicolaus Copernicus University in Torun","award":["4101:00000066"],"award-info":[{"award-number":["4101:00000066"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Materials"],"abstract":"<jats:p>In this paper, a highly efficient and straightforward method for synthesizing novel Schiff bases was developed by reacting selected biogenic amines with sodium 2-formylbenzene sulfonate and sodium 3-formylbenzene sulfonate. 1H and 13C NMR, IR spectroscopy, and high-resolution mass spectrometry were used to characterize the new compounds. The main advantages of the proposed procedure include simple reagents and reactions carried out in water or methanol and at room temperature, which reduces time and energy. Moreover, it was shown that the obtained water-soluble Schiff bases are stable in aqueous solution for at least seven days. Additionally, the antioxidant and antimicrobial activity of synthesized Schiff bases were tested.<\/jats:p>","DOI":"10.3390\/ma17020520","type":"journal-article","created":{"date-parts":[[2024,1,22]],"date-time":"2024-01-22T11:36:41Z","timestamp":1705923401000},"page":"520","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["New Water-Soluble (Iminomethyl)benzenesulfonates Derived from Biogenic Amines for Potential Biological Applications"],"prefix":"10.3390","volume":"17","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0002-0338","authenticated-orcid":false,"given":"Anna","family":"Kmieciak","sequence":"first","affiliation":[{"name":"Faculty of Chemistry, Nicolaus Copernicus University in Torun, 7 Gagarin Str., 87-100 Torun, Poland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4337-5676","authenticated-orcid":false,"given":"Marek P.","family":"Krzemi\u0144ski","sequence":"additional","affiliation":[{"name":"Faculty of Chemistry, Nicolaus Copernicus University in Torun, 7 Gagarin Str., 87-100 Torun, Poland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anastasiia","family":"Hodii","sequence":"additional","affiliation":[{"name":"Faculty of Chemistry, Nicolaus Copernicus University in Torun, 7 Gagarin Str., 87-100 Torun, Poland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5328-2927","authenticated-orcid":false,"given":"Damian","family":"Gorczyca","sequence":"additional","affiliation":[{"name":"Faculty of Medicine, Lazarski University, 43 \u015awieradowska Str., 02-662 Warsaw, Poland"},{"name":"LymeLab Pharma, Kochanowskiego 49A Str., 01-864 Warsaw, Poland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5004-0161","authenticated-orcid":false,"given":"Aneta","family":"Jastrz\u0119bska","sequence":"additional","affiliation":[{"name":"Faculty of Chemistry, Nicolaus Copernicus University in Torun, 7 Gagarin Str., 87-100 Torun, Poland"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1968","published-online":{"date-parts":[[2024,1,22]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"726","DOI":"10.1002\/ajoc.201300012","article-title":"Catalytic methods for imine synthesis","volume":"2","author":"Patil","year":"2013","journal-title":"Asian J. 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