Debu Jana, Manaswitha Todupunuri, Mohd Shavez and Samar K. Das*,
{"title":"三配体与CoCl2·6H2O在水溶液中的有效络合:抑制CoOx的电化学生成","authors":"Debu Jana, Manaswitha Todupunuri, Mohd Shavez and Samar K. Das*, ","doi":"10.1021/acs.inorgchem.5c0053510.1021/acs.inorgchem.5c00535","DOIUrl":null,"url":null,"abstract":"<p >In this report, we have demonstrated an effective complexation of <b>TrisH</b><sub><b>3</b></sub> (tris(hydroxymethyl)aminomethane) ligand with Co(II) when it is added to a sodium acetate containing aqueous solution of CoCl<sub>2</sub>·6H<sub>2</sub>O, leading to the formation of a Co(II)-coordination complex, [Co<sup>II</sup>(TrisH<sub>2</sub>)(TrisH<sub>3</sub>)(CH<sub>3</sub>COO) (H<sub>2</sub>O)] (<b>CoT</b>), in the resultant solution at a pH value of 8.6. We could characterize the <b>CoT</b> complex in its solution state by diverse spectral analyses followed by its validation using computational (density functional theory (DFT)) studies. The Job plot from UV–visible data indicates a 2:1 Tris/Co coordination complex in the aqueous solution of <b>TrisH</b><sub><b>3</b></sub> and CoCl<sub>2</sub>·6H<sub>2</sub>O. Interestingly, this complex (<b>CoT</b>) in its solution state inhibits the formation of CoO<sub><i>x</i></sub> during electrochemical studies, whereas the aqueous solution of CoCl<sub>2</sub>·6H<sub>2</sub>O <i>per se</i> generates CoO<sub><i>x</i></sub> <i>in situ</i>. The relevant electrochemical and spectroscopic studies, including controlled experiments, have been performed in this work.</p>","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":"64 16","pages":"7841–7845 7841–7845"},"PeriodicalIF":4.7000,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effective Complexation of Tris-Ligand with CoCl2·6H2O in an Aqueous Solution: Suppressing Electrochemical Formation of CoOx\",\"authors\":\"Debu Jana, Manaswitha Todupunuri, Mohd Shavez and Samar K. Das*, \",\"doi\":\"10.1021/acs.inorgchem.5c0053510.1021/acs.inorgchem.5c00535\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In this report, we have demonstrated an effective complexation of <b>TrisH</b><sub><b>3</b></sub> (tris(hydroxymethyl)aminomethane) ligand with Co(II) when it is added to a sodium acetate containing aqueous solution of CoCl<sub>2</sub>·6H<sub>2</sub>O, leading to the formation of a Co(II)-coordination complex, [Co<sup>II</sup>(TrisH<sub>2</sub>)(TrisH<sub>3</sub>)(CH<sub>3</sub>COO) (H<sub>2</sub>O)] (<b>CoT</b>), in the resultant solution at a pH value of 8.6. We could characterize the <b>CoT</b> complex in its solution state by diverse spectral analyses followed by its validation using computational (density functional theory (DFT)) studies. The Job plot from UV–visible data indicates a 2:1 Tris/Co coordination complex in the aqueous solution of <b>TrisH</b><sub><b>3</b></sub> and CoCl<sub>2</sub>·6H<sub>2</sub>O. Interestingly, this complex (<b>CoT</b>) in its solution state inhibits the formation of CoO<sub><i>x</i></sub> during electrochemical studies, whereas the aqueous solution of CoCl<sub>2</sub>·6H<sub>2</sub>O <i>per se</i> generates CoO<sub><i>x</i></sub> <i>in situ</i>. The relevant electrochemical and spectroscopic studies, including controlled experiments, have been performed in this work.</p>\",\"PeriodicalId\":40,\"journal\":{\"name\":\"Inorganic Chemistry\",\"volume\":\"64 16\",\"pages\":\"7841–7845 7841–7845\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-04-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.inorgchem.5c00535\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.inorgchem.5c00535","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Effective Complexation of Tris-Ligand with CoCl2·6H2O in an Aqueous Solution: Suppressing Electrochemical Formation of CoOx
In this report, we have demonstrated an effective complexation of TrisH3 (tris(hydroxymethyl)aminomethane) ligand with Co(II) when it is added to a sodium acetate containing aqueous solution of CoCl2·6H2O, leading to the formation of a Co(II)-coordination complex, [CoII(TrisH2)(TrisH3)(CH3COO) (H2O)] (CoT), in the resultant solution at a pH value of 8.6. We could characterize the CoT complex in its solution state by diverse spectral analyses followed by its validation using computational (density functional theory (DFT)) studies. The Job plot from UV–visible data indicates a 2:1 Tris/Co coordination complex in the aqueous solution of TrisH3 and CoCl2·6H2O. Interestingly, this complex (CoT) in its solution state inhibits the formation of CoOx during electrochemical studies, whereas the aqueous solution of CoCl2·6H2O per se generates CoOxin situ. The relevant electrochemical and spectroscopic studies, including controlled experiments, have been performed in this work.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.