{"title":"混合给体氨基和氧配体的新型不对称氧钒配合物","authors":"S. Mohebi, D. Boghaei","doi":"10.1081/SIM-120030444","DOIUrl":null,"url":null,"abstract":"Abstract The novel, unsymmetrical, mixed‐donor, tetradentate amido, and oxo complexes of V(IV) of the general formula VOL x were synthesized by a nontemplate method and characterized by physico‐chemical methods. The ligands were prepared by a two‐stage aldol condensation reaction in the molar ratio 1:1 of 2‐hydroxybenzaldehyde, 2′‐hydroxyacetophenone, or 2′,4′‐dihydroxyacetophenone and 1,2‐diaminopropane of the general formula HA x (x = 1–3) as precursors. The tetradentate mixed donor ligands of the general formula H2L x (x = 1–6) were obtained by condensation reaction of precursors with appropriate ketone or aldehyde. The synthesis of the ligand system, described here, is an efficient and easy method with the advantages of high yield, selectivity, and short reaction times. Only a brown polymeric form was obtained for VOL2 and green monomeric forms were obtained for VOL x , x = 1, 3–5, while in the presence of strong field ligands only monomeric forms were obtained. These observations suggest that monomeric forms of oxovanadium(IV) complexes exhibit a coordination number of five with N2O3 donor sets and the polymeric form exhibits a coordination number of six with N2O4 donor sets. Analytical data, 1H NMR, IR, UV–VIS spectra, and elemental analyses confirm the nature of the products.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"133 1","pages":"611 - 626"},"PeriodicalIF":0.0000,"publicationDate":"2004-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"New Unsymmetrical Oxovanadium(IV) Complexes of Mixed‐Donor Amido and Oxo Ligands\",\"authors\":\"S. Mohebi, D. Boghaei\",\"doi\":\"10.1081/SIM-120030444\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract The novel, unsymmetrical, mixed‐donor, tetradentate amido, and oxo complexes of V(IV) of the general formula VOL x were synthesized by a nontemplate method and characterized by physico‐chemical methods. The ligands were prepared by a two‐stage aldol condensation reaction in the molar ratio 1:1 of 2‐hydroxybenzaldehyde, 2′‐hydroxyacetophenone, or 2′,4′‐dihydroxyacetophenone and 1,2‐diaminopropane of the general formula HA x (x = 1–3) as precursors. The tetradentate mixed donor ligands of the general formula H2L x (x = 1–6) were obtained by condensation reaction of precursors with appropriate ketone or aldehyde. The synthesis of the ligand system, described here, is an efficient and easy method with the advantages of high yield, selectivity, and short reaction times. Only a brown polymeric form was obtained for VOL2 and green monomeric forms were obtained for VOL x , x = 1, 3–5, while in the presence of strong field ligands only monomeric forms were obtained. These observations suggest that monomeric forms of oxovanadium(IV) complexes exhibit a coordination number of five with N2O3 donor sets and the polymeric form exhibits a coordination number of six with N2O4 donor sets. Analytical data, 1H NMR, IR, UV–VIS spectra, and elemental analyses confirm the nature of the products.\",\"PeriodicalId\":22160,\"journal\":{\"name\":\"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry\",\"volume\":\"133 1\",\"pages\":\"611 - 626\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2004-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1081/SIM-120030444\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1081/SIM-120030444","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
摘要
摘要采用非模板法合成了通式VOL x中新型的不对称、混合给体、四齿胺和氧配合物,并用物理化学方法对其进行了表征。以2 -羟基苯甲醛、2 ' -羟基苯乙酮或2 ',4 ' -二羟基苯乙酮和1,2 -二氨基丙烷为前体(x = 1 - 3),以摩尔比为1:1的两级醛醇缩合反应制备配体。通过前驱体与适当的酮或醛缩合反应,得到了通式H2L x (x = 1-6)的四齿混合给体配体。本文所描述的配体体系的合成是一种高效、简便的方法,具有收率高、选择性好、反应时间短等优点。VOL2只得到棕色的聚合物形式,而VOL x, x = 1,3 - 5只得到绿色的单体形式,而在强场配体存在下只得到单体形式。这些观察结果表明,氧化钒(IV)配合物的单体形式与N2O3供体集的配位数为5,聚合物形式与N2O4供体集的配位数为6。分析数据,1H NMR, IR, UV-VIS光谱和元素分析证实了产品的性质。
New Unsymmetrical Oxovanadium(IV) Complexes of Mixed‐Donor Amido and Oxo Ligands
Abstract The novel, unsymmetrical, mixed‐donor, tetradentate amido, and oxo complexes of V(IV) of the general formula VOL x were synthesized by a nontemplate method and characterized by physico‐chemical methods. The ligands were prepared by a two‐stage aldol condensation reaction in the molar ratio 1:1 of 2‐hydroxybenzaldehyde, 2′‐hydroxyacetophenone, or 2′,4′‐dihydroxyacetophenone and 1,2‐diaminopropane of the general formula HA x (x = 1–3) as precursors. The tetradentate mixed donor ligands of the general formula H2L x (x = 1–6) were obtained by condensation reaction of precursors with appropriate ketone or aldehyde. The synthesis of the ligand system, described here, is an efficient and easy method with the advantages of high yield, selectivity, and short reaction times. Only a brown polymeric form was obtained for VOL2 and green monomeric forms were obtained for VOL x , x = 1, 3–5, while in the presence of strong field ligands only monomeric forms were obtained. These observations suggest that monomeric forms of oxovanadium(IV) complexes exhibit a coordination number of five with N2O3 donor sets and the polymeric form exhibits a coordination number of six with N2O4 donor sets. Analytical data, 1H NMR, IR, UV–VIS spectra, and elemental analyses confirm the nature of the products.