{"title":"新型MCl3 (M = Y, Dy, Pr)水杨酸、马来酸、酞酸、苯基磺酰基和磷酸配合物及加合物的合成与红外研究","authors":"Dame Seye","doi":"10.19080/omcij.2019.09.555761","DOIUrl":null,"url":null,"abstract":"Nine rare earth complexes have been synthesized from reaction carried in common organic solvent between salicylate, maleate, phtalate, phenylsulfonate or phosphate ammonium salt and MCl3 (M = Y, Dy, Pr). All compounds have been structurally characterized by infrared. Structures involving the complex anions have been proposed. The suggested structures are discrete or of double metallic components type. The oxyanions behave towards metallic centres as monodentate, monochelating or monochelating and monodentate ligands. The coordination number at rare earth metal atoms vary from five (5) for Pr and Dy to twelve (12) for Dy. For compounds containing a protonated amine, when the possible hydrogen bonding interactions are considered supramolecular architectures may be","PeriodicalId":19547,"journal":{"name":"Organic & Medicinal Chemistry International Journal","volume":"26 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New MCl3 (M = Y, Dy, Pr) Salicylato, Maleato, Phtalato, Phenylsufonato and Phosphato Complexes and Adducts: Synthesis and Infrared Study\",\"authors\":\"Dame Seye\",\"doi\":\"10.19080/omcij.2019.09.555761\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Nine rare earth complexes have been synthesized from reaction carried in common organic solvent between salicylate, maleate, phtalate, phenylsulfonate or phosphate ammonium salt and MCl3 (M = Y, Dy, Pr). All compounds have been structurally characterized by infrared. Structures involving the complex anions have been proposed. The suggested structures are discrete or of double metallic components type. The oxyanions behave towards metallic centres as monodentate, monochelating or monochelating and monodentate ligands. The coordination number at rare earth metal atoms vary from five (5) for Pr and Dy to twelve (12) for Dy. For compounds containing a protonated amine, when the possible hydrogen bonding interactions are considered supramolecular architectures may be\",\"PeriodicalId\":19547,\"journal\":{\"name\":\"Organic & Medicinal Chemistry International Journal\",\"volume\":\"26 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Medicinal Chemistry International Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.19080/omcij.2019.09.555761\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Medicinal Chemistry International Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19080/omcij.2019.09.555761","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
以水杨酸盐、马来酸盐、邻苯二甲酸盐、苯基磺酸盐或磷酸铵盐与mc3 (M = Y, Dy, Pr)为原料,在常见有机溶剂中合成了9种稀土配合物。所有化合物都用红外光谱进行了结构表征。已经提出了涉及复合阴离子的结构。所建议的结构是离散的或双金属构件型的。氧阴离子对金属中心表现为单齿、单螯合或单螯合和单齿配体。稀土金属原子的配位数从Pr和Dy的5(5)到Dy的12(12)不等。对于含有质子化胺的化合物,当可能的氢键相互作用被认为是超分子结构时
New MCl3 (M = Y, Dy, Pr) Salicylato, Maleato, Phtalato, Phenylsufonato and Phosphato Complexes and Adducts: Synthesis and Infrared Study
Nine rare earth complexes have been synthesized from reaction carried in common organic solvent between salicylate, maleate, phtalate, phenylsulfonate or phosphate ammonium salt and MCl3 (M = Y, Dy, Pr). All compounds have been structurally characterized by infrared. Structures involving the complex anions have been proposed. The suggested structures are discrete or of double metallic components type. The oxyanions behave towards metallic centres as monodentate, monochelating or monochelating and monodentate ligands. The coordination number at rare earth metal atoms vary from five (5) for Pr and Dy to twelve (12) for Dy. For compounds containing a protonated amine, when the possible hydrogen bonding interactions are considered supramolecular architectures may be