Xu Yingying, Laijin Tian, Wenchao Ding, Han Lu, Wugai An
{"title":"1.2.5. Synthesis, crystal structure and catalytic activity of 2-methoxycarbonylethyldichlorotin hydroxide","authors":"Xu Yingying, Laijin Tian, Wenchao Ding, Han Lu, Wugai An","doi":"10.21060/cis.v1i2.2001","DOIUrl":null,"url":null,"abstract":"Abstract: 2-methoxycarbonylethyldichlorotin hydroxide, CH 3 OCOCH 2 CH 2 SnCl 2 (OH) ( 1), has been synthesized by hydrolysis reaction and characterized by elemental analysis, FTIR, 1 H NMR spectroscopy, and X-ray single crystal diffraction. Compound 1 is a centrosymmetric dimmer, and the tin atom approximates to octahedral geometry via an intramolecular carbonyl- to-tin coordination and hydroxo-bridging. The compound display high selectivity and good catalysis activity on the transesterification reaction of ethyl acetoacetate with an alcohol. Supporting information: FT-IR, 1 H NMR, X-Ray, GC/MS analyses, Cif file.","PeriodicalId":10648,"journal":{"name":"Communications in Inorganic Synthesis","volume":"43 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications in Inorganic Synthesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21060/cis.v1i2.2001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Abstract: 2-methoxycarbonylethyldichlorotin hydroxide, CH 3 OCOCH 2 CH 2 SnCl 2 (OH) ( 1), has been synthesized by hydrolysis reaction and characterized by elemental analysis, FTIR, 1 H NMR spectroscopy, and X-ray single crystal diffraction. Compound 1 is a centrosymmetric dimmer, and the tin atom approximates to octahedral geometry via an intramolecular carbonyl- to-tin coordination and hydroxo-bridging. The compound display high selectivity and good catalysis activity on the transesterification reaction of ethyl acetoacetate with an alcohol. Supporting information: FT-IR, 1 H NMR, X-Ray, GC/MS analyses, Cif file.