K. Karpagavel, Aron Hailemichael, Tewelde Sahle, Alexander Berhane, A. Manohar
{"title":"二硫代氨基甲酸盐配体转化为硫酸盐阴离子:光谱、x射线晶体学和基于价键和(VBS)的研究","authors":"K. Karpagavel, Aron Hailemichael, Tewelde Sahle, Alexander Berhane, A. Manohar","doi":"10.29055/JCCS/681","DOIUrl":null,"url":null,"abstract":"Copper(II)dithiocarbamate complexes,[Cu(dtc)2], (dtc = N-methyl, Nethanoldithio-carbamate, diethanoldithiocarbamte, piperidinedithiocarbamate, piperazinedithiocarbamate, morphlinedithiocarbamate, diisopropyldithiocarbamate, diethyldithiocarbamate, dimethyldithiocarbamate) were treated with 2,2’-bipyridine in ethanol or ethanol/chloroform medium under refluxing conditions. The products were analyzed by IR and UV-Visible spectra, electrical conductivity, elemental analysis and single crystal X-ray crystallography. Characterization studies showed that the product, [Cu(2,2’-bipy)(H2O)2]SO4, is identical in all the reactions. Dithiocarbamate ligand of each copper complex oxidized to SO4 ion. Single crystal X-ray structure of [Cu(2,2’-bipy)(H2O)2]SO4 indicate that the central copper atom is in a distorted octahedral environment. Valence Bond Sum (VBS) value was also calculated for the crystal structure of [Cu(2,2’-bipy)(H2O)2]SO4 and the results are reported in this paper. The VBS value was found to be equivalent to 1.96, supporting the correctness of the determined crystal structure and the value is close to +2, which is the formal oxidation state of copper.","PeriodicalId":15337,"journal":{"name":"Journal of Chemistry and Chemical Sciences","volume":"53 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Conversion of Dithiocarbamate Ligand into Sulphate Anion : Spectroscopy, X-ray Crystallography and\\nValence Bond Sum (VBS) Based Investigations\",\"authors\":\"K. Karpagavel, Aron Hailemichael, Tewelde Sahle, Alexander Berhane, A. Manohar\",\"doi\":\"10.29055/JCCS/681\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Copper(II)dithiocarbamate complexes,[Cu(dtc)2], (dtc = N-methyl, Nethanoldithio-carbamate, diethanoldithiocarbamte, piperidinedithiocarbamate, piperazinedithiocarbamate, morphlinedithiocarbamate, diisopropyldithiocarbamate, diethyldithiocarbamate, dimethyldithiocarbamate) were treated with 2,2’-bipyridine in ethanol or ethanol/chloroform medium under refluxing conditions. The products were analyzed by IR and UV-Visible spectra, electrical conductivity, elemental analysis and single crystal X-ray crystallography. Characterization studies showed that the product, [Cu(2,2’-bipy)(H2O)2]SO4, is identical in all the reactions. Dithiocarbamate ligand of each copper complex oxidized to SO4 ion. Single crystal X-ray structure of [Cu(2,2’-bipy)(H2O)2]SO4 indicate that the central copper atom is in a distorted octahedral environment. Valence Bond Sum (VBS) value was also calculated for the crystal structure of [Cu(2,2’-bipy)(H2O)2]SO4 and the results are reported in this paper. The VBS value was found to be equivalent to 1.96, supporting the correctness of the determined crystal structure and the value is close to +2, which is the formal oxidation state of copper.\",\"PeriodicalId\":15337,\"journal\":{\"name\":\"Journal of Chemistry and Chemical Sciences\",\"volume\":\"53 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemistry and Chemical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.29055/JCCS/681\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemistry and Chemical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29055/JCCS/681","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Conversion of Dithiocarbamate Ligand into Sulphate Anion : Spectroscopy, X-ray Crystallography and
Valence Bond Sum (VBS) Based Investigations
Copper(II)dithiocarbamate complexes,[Cu(dtc)2], (dtc = N-methyl, Nethanoldithio-carbamate, diethanoldithiocarbamte, piperidinedithiocarbamate, piperazinedithiocarbamate, morphlinedithiocarbamate, diisopropyldithiocarbamate, diethyldithiocarbamate, dimethyldithiocarbamate) were treated with 2,2’-bipyridine in ethanol or ethanol/chloroform medium under refluxing conditions. The products were analyzed by IR and UV-Visible spectra, electrical conductivity, elemental analysis and single crystal X-ray crystallography. Characterization studies showed that the product, [Cu(2,2’-bipy)(H2O)2]SO4, is identical in all the reactions. Dithiocarbamate ligand of each copper complex oxidized to SO4 ion. Single crystal X-ray structure of [Cu(2,2’-bipy)(H2O)2]SO4 indicate that the central copper atom is in a distorted octahedral environment. Valence Bond Sum (VBS) value was also calculated for the crystal structure of [Cu(2,2’-bipy)(H2O)2]SO4 and the results are reported in this paper. The VBS value was found to be equivalent to 1.96, supporting the correctness of the determined crystal structure and the value is close to +2, which is the formal oxidation state of copper.