Nishant Shekhar, Rajesh Kumar, Riya Kumari, Ram Nayan Gautam, Diptee Mitra, Ramesh Chandra, Arti Srivastava, M. K. Bharty
{"title":"Pyridyl Thiosemicarbazone Complexes of Ni (II), Cu (II), and Zn (II): Structural Insights and Neuropharmacological Activity","authors":"Nishant Shekhar, Rajesh Kumar, Riya Kumari, Ram Nayan Gautam, Diptee Mitra, Ramesh Chandra, Arti Srivastava, M. K. Bharty","doi":"10.1002/aoc.70650","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Thiosemicarbazone-based metal complexes have attracted considerable attention due to their rich coordination chemistry and emerging biological relevance; however, systematic correlations between their structural features and neuropharmacological activities remain limited. In this work, three metal complexes, [Ni(HcpmTsc)<sub>2</sub>] (<b>1</b>), [Cu(HcpmTsc)(Cl)] (<b>2</b>), and [Zn(HcpmTsc)<sub>2</sub>] (<b>3</b>), derived from <i>N</i>-(2-chlorophenyl)-2-(pyridyl methylene) thiosemicarbazone (<b>H</b><sub><b>2</b></sub><b>cpmTsc</b>), were synthesized and comprehensively characterized using spectral techniques. In addition, complexes <b>1</b> and <b>3</b> were characterized by single-crystal X-ray diffraction, whereas the crystal structure of complex <b>2</b> had been reported earlier; however, its sedative and anxiolytic activities have been evaluated for the first time in the present study. Structural analyses revealed distorted octahedral geometries for complexes <b>1</b> and <b>3,</b> with the ligand acting as a uninegative tridentate donor in all cases. The crystal structures reveal extended supramolecular assemblies stabilized by intermolecular C-H···N and C-H···S interactions. Photoluminescence studies demonstrated that the ligand and all complexes exhibit fluorescent behavior. To address the paucity of neuropharmacological investigations on such systems, the synthesized compounds were evaluated for sedative and anxiolytic activities using established animal models. The results indicated notable sedative and anxiolytic effects mediated predominantly through GABA<sub>A</sub> receptor pathways, with [Ni(HcpmTsc)<sub>2</sub>] (<b>1</b>) showing the highest activity. Molecular docking studies supported these findings by confirming favorable receptor interactions. Overall, this study highlights the therapeutic potential of these complexes as candidates for neuropharmacological development.</p>\n </div>","PeriodicalId":8344,"journal":{"name":"Applied Organometallic Chemistry","volume":"40 10","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2026-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Organometallic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/aoc.70650","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
Thiosemicarbazone-based metal complexes have attracted considerable attention due to their rich coordination chemistry and emerging biological relevance; however, systematic correlations between their structural features and neuropharmacological activities remain limited. In this work, three metal complexes, [Ni(HcpmTsc)2] (1), [Cu(HcpmTsc)(Cl)] (2), and [Zn(HcpmTsc)2] (3), derived from N-(2-chlorophenyl)-2-(pyridyl methylene) thiosemicarbazone (H2cpmTsc), were synthesized and comprehensively characterized using spectral techniques. In addition, complexes 1 and 3 were characterized by single-crystal X-ray diffraction, whereas the crystal structure of complex 2 had been reported earlier; however, its sedative and anxiolytic activities have been evaluated for the first time in the present study. Structural analyses revealed distorted octahedral geometries for complexes 1 and 3, with the ligand acting as a uninegative tridentate donor in all cases. The crystal structures reveal extended supramolecular assemblies stabilized by intermolecular C-H···N and C-H···S interactions. Photoluminescence studies demonstrated that the ligand and all complexes exhibit fluorescent behavior. To address the paucity of neuropharmacological investigations on such systems, the synthesized compounds were evaluated for sedative and anxiolytic activities using established animal models. The results indicated notable sedative and anxiolytic effects mediated predominantly through GABAA receptor pathways, with [Ni(HcpmTsc)2] (1) showing the highest activity. Molecular docking studies supported these findings by confirming favorable receptor interactions. Overall, this study highlights the therapeutic potential of these complexes as candidates for neuropharmacological development.
期刊介绍:
All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.