Characterization, Antibacterial Evaluation and Computational Study of Synthesized 4,5-bis(Hydroxymethyl)-2-Methylpyridin-3-ol Tetraphenylborate Ion-Pair Complex
Ahmed H. Bakheit, Mohamed H. Al-Agamy, Rashad Al-Salahi, Essam Ali, Haitham Alrabiah, Gamal A.E. Mostafa
{"title":"Characterization, Antibacterial Evaluation and Computational Study of Synthesized 4,5-bis(Hydroxymethyl)-2-Methylpyridin-3-ol Tetraphenylborate Ion-Pair Complex","authors":"Ahmed H. Bakheit, Mohamed H. Al-Agamy, Rashad Al-Salahi, Essam Ali, Haitham Alrabiah, Gamal A.E. Mostafa","doi":"10.1002/open.202400422","DOIUrl":null,"url":null,"abstract":"<p>The synthesis of 4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol tetraphenylborate complex in water using an anion exchange process yielded more than 76 %. The resulting white complex was obtained and characterized using various spectroscopic and analytical techniques, including ultraviolet, infrared radiation (IR), mass, elemental analysis, and nuclear magnetic resonance (NMR). The antimicrobial activity of the formed ion-associate complex was evaluated. The structural, electrical, and bonding properties of a novel pyridoxine-tetraphenylborate ion-pair complex was explored using B3LYP/6-311G(d,p) DFT simulations. Geometries designed for negative complexation energy showed thermodynamically beneficial complex formation. Reduced density gradient (RDG) analysis and non-covalent interaction (NCI) plots showed that van der Waals forces are essential to complex stability. Quantum Theory of Atoms in Molecules (QTAIM) study detected weak and moderate hydrogen bonds in the complex using bond critical point (BCP) features. These results reveal how molecules form and stabilize the pyridoxine-tetraphenylborate ion-pair complex. To know the interaction between receptors and bioactive chemicals, one must understand the mechanism of the ionic complexes formed between bioactive chemicals and/or organic molecules.</p>","PeriodicalId":9831,"journal":{"name":"ChemistryOpen","volume":"14 3","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/open.202400422","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistryOpen","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/open.202400422","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The synthesis of 4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol tetraphenylborate complex in water using an anion exchange process yielded more than 76 %. The resulting white complex was obtained and characterized using various spectroscopic and analytical techniques, including ultraviolet, infrared radiation (IR), mass, elemental analysis, and nuclear magnetic resonance (NMR). The antimicrobial activity of the formed ion-associate complex was evaluated. The structural, electrical, and bonding properties of a novel pyridoxine-tetraphenylborate ion-pair complex was explored using B3LYP/6-311G(d,p) DFT simulations. Geometries designed for negative complexation energy showed thermodynamically beneficial complex formation. Reduced density gradient (RDG) analysis and non-covalent interaction (NCI) plots showed that van der Waals forces are essential to complex stability. Quantum Theory of Atoms in Molecules (QTAIM) study detected weak and moderate hydrogen bonds in the complex using bond critical point (BCP) features. These results reveal how molecules form and stabilize the pyridoxine-tetraphenylborate ion-pair complex. To know the interaction between receptors and bioactive chemicals, one must understand the mechanism of the ionic complexes formed between bioactive chemicals and/or organic molecules.
期刊介绍:
ChemistryOpen is a multidisciplinary, gold-road open-access, international forum for the publication of outstanding Reviews, Full Papers, and Communications from all areas of chemistry and related fields. It is co-owned by 16 continental European Chemical Societies, who have banded together in the alliance called ChemPubSoc Europe for the purpose of publishing high-quality journals in the field of chemistry and its border disciplines. As some of the governments of the countries represented in ChemPubSoc Europe have strongly recommended that the research conducted with their funding is freely accessible for all readers (Open Access), ChemPubSoc Europe was concerned that no journal for which the ethical standards were monitored by a chemical society was available for such papers. ChemistryOpen fills this gap.