{"title":"C-H Bond Chlorination and Bromination Using Water Soluble Nickel (II) guanidine Complexes","authors":"Jaipriya Khatri, Vasanthapandiyan Mari, Aniruddha Sarkar, Naiwrit Karmodak, Basab Bijayi Dhar","doi":"10.1039/d4dt02783c","DOIUrl":null,"url":null,"abstract":"The water-soluble Nickel(II)-guanidine-based complexes successfully catalyzed the C-H chlorination of a series of hydrocarbons in the presence of NaOCl and acetic acid in water-chloroform (7:3, biphasic condition) at room temperature. Majorly chlorinated products (TON ~680 for cyclohexane) were obtained. Furthermore, C-H bond bromination of cyclohexane, n-hexane, and toluene was also carried out using in situ generation of NaOBr. These putative formations of Ni(III) species were characterized by electron paramagnetic resonance (EPR) spectroscopy, and the plausible mechanism for chlorination was confirmed by DFT calculation.","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":"135 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4dt02783c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
The water-soluble Nickel(II)-guanidine-based complexes successfully catalyzed the C-H chlorination of a series of hydrocarbons in the presence of NaOCl and acetic acid in water-chloroform (7:3, biphasic condition) at room temperature. Majorly chlorinated products (TON ~680 for cyclohexane) were obtained. Furthermore, C-H bond bromination of cyclohexane, n-hexane, and toluene was also carried out using in situ generation of NaOBr. These putative formations of Ni(III) species were characterized by electron paramagnetic resonance (EPR) spectroscopy, and the plausible mechanism for chlorination was confirmed by DFT calculation.
期刊介绍:
Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.