کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1305711 | 1499178 | 2014 | 12 صفحه PDF | دانلود رایگان |
y (x = y = 3, 2, 1.50, 1.45, 1 and 0 and x = 3, y = 2) of a triprotic imidazole containing Schiff base ligand. Effect of protonation state on supramolec Synthesis, structure and supramolecular features of cobalt(III) and cobalt(II) complexes, [CoHxL](ClO4)y (x = y = 3, 2, 1.50, 1.45, 1 and 0 and x = 3, y = 2) of a triprotic imidazole containing Schiff base ligand. Effect of protonation state on supramolec](/preview/png/1305711.png)
• The study prepares ten cobalt complexes of one triprotic, H3L, hexadentate ligand.
• Structures of Co(III) and Co(II) complexes of H L are compared.
• The structure of the Co(III) complexes of each of the four protonated states of the ligand are determined.
• A number of supramolecular topologies, dimeric, 1D chain, tetrahedral cluster and 2D sheet, are described.
• Two examples of chiral recognition are observed.
Aerial reaction of cobalt(II) perchlorate with H3(1) {H3(1) is the tripodal ligand derived from the condensation of tris(2-aminoethyl)amine with three equivalents of 4-methyl-5-imidazolecarboxaldehyde} in acidic methanol results in isolation of both the orange [CoH3(1)](ClO4)2 (trace) and red [CoH3(1)](ClO4)3 (2 pseudopolymorphs). An analogous reaction in methanol gives [CoH2(1)](ClO4)2. Reaction of [CoH2(1)](ClO4)2 (generated in situ) with aqueous sodium hydroxide gives [CoH(1)](ClO4) (two pseudopolymorphs) and a trace amount of [CoH1.45(1)](ClO4)1.45. Reaction of [CoH3(1)](ClO4)3 with 1.5 equivalents of hydroxide gives [CoH1.5(1)](ClO4)1.5. Reaction of [CoH(1)](ClO4) with methanolic potassium hydroxide in acetonitrile gave [Co(1)] (two pseudopolymorphs). Complexes were characterized by EA and IR if available in sufficient amounts. All ten complexes were structurally characterized and their metrical parameters are consistent with a high spin cobalt(II) for [CoH3(1)](ClO4)2 and low spin cobalt(III) for all of the cobalt(III) complexes. [CoH3(1)](ClO4)2 and one polymorph of [CoH3(1)](ClO4)3 dimerize by hydrogen bonding through three perchlorate anions. [CoH2(1)](ClO4)2 and one of the pseudopolymorphs of [CoH(1)](ClO4) form intermolecular imidazole-H…imidazolate hydrogen bonds resulting in hetero and homochiral 1D zig-zag chains, respectively. [CoH1.5(1)](ClO4)1.5 forms a tetrahedral array of octahedral cobalt complexes held together by intermolecular imidazole-H…imidazolate hydrogen bonds. [CoH1.45(1)](ClO4)1.45 forms a hexameric structure with a large central channel containing solvent and perchlorate anions. [CoH(1)](ClO4) and both polymorphs of [Co(1)] form no intermolecular imidazole-H…imidazolate hydrogen bonds but do exhibit extensive hydrogen bond formation with water.
Cobalt(III) complexes of a triprotic ligand, H3L, have been isolated and structurally characterized for each of the following protonation states of the ligand, H3L, H2L−, H1.5L1.5−, H1.45L1.55−, HL2− and L3−. A variety of topologies, dimeric, 1D zig-zag, tetrahedral and 2D sheets are observed in the structures.Figure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 410, 30 January 2014, Pages 94–105