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dc.creatorESTEVEZ HERNANDEZ, O.-
dc.creatorDUQUE, J.-
dc.creatorREGUERA, E.-
dc.date2012-03-23T01:12:11Z-
dc.date2012-03-23T01:12:11Z-
dc.date2011-06-03-
dc.date.accessioned2013-01-16T09:54:12Z-
dc.date.available2013-01-16T09:54:12Z-
dc.date.issued2013-01-16-
dc.identifierVol. 32, No. 3, June 2011, 213–222-
dc.identifierhttp://hdl.handle.net/123456789/287-
dc.identifier.urihttp://www.repositoriodigital.ipn.mx/handle/123456789/10782-
dc.descriptionThe structural features of two series of 1-furoylthioureas 3-monosubstituted (Series 1) and 3,3-disubstituted (Series 2) 1-furoylthioureas and their CdCl2 complexes are discussed. The coordination strength through the sulfur atom is determined by the ligand structure. In Series 1 ligands, the carbonyl group and the proton on N2 are engaged in a strong hydrogen bond interaction. This leads to an “S”-shaped conformation type of the C=O and C=S groups where these donor sites reach a maximum separation. In the absence of that hydrogen bridge in 3,3-disubstituted derivatives, the C=O and C=S groups can adopt a “U”-shaped conformation type. This feature is also observed for two novel crystal structures of 1-(2-furoyl)-3-(2- hydroxyethyl)thiourea and 1-furoyl-3-ethyl-3-phenylthiourea, as determined by X-ray diffractometry and reported here. Emphasis is placed on the relationship between structural features of these ligands and their behavior as cadmium ionophores in potentiometric and amperometric sensors.-
dc.languageen_US-
dc.publisherJournal of Sulfur Chemistry-
dc.subjectfuroylthioureas-
dc.subjectCd(II) complexes-
dc.subjectcrystal structure-
dc.subjectRaman-
dc.subjectionophores-
dc.titleStructural features of 1-furoylthioureas 3-monosubstituted and 3,3-disubstituted: coordination to cadmium and analytical applications-
dc.typeArticle-
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