A new compound of general formula {[(H2O)2K(μ-H2O)Sr]@[Cr(C2O4)3]}n (1) has been synthesized in water and characterized by elemental and thermal analyses, EDX, IR and UV-Vis spectroscopies and by single crystal X-ray...A new compound of general formula {[(H2O)2K(μ-H2O)Sr]@[Cr(C2O4)3]}n (1) has been synthesized in water and characterized by elemental and thermal analyses, EDX, IR and UV-Vis spectroscopies and by single crystal X-ray structure determination. Compound 1 crystallizes in the chiral space group Fdd2 of orthorhombic system with a = 14.110 (4) ?, b = 36.074 (11)?, c =11.034 (3)? and Z = 16. Compound 1 is a coordination polymer in which the three-dimensional lattice framework is realized by the interconnectivity between K+ cations, Sr2+ cations, aqua ligands and [Cr(C2O4)3]3– complex anions. The asymmetric unit of 1 consists of one cationic motif formally written [(H2O)2K(μ-H2O)Sr]3+ and one anionic entity, [Cr(C2O4)3]3–. The K+ and Sr2+ ions in the cationic motif are both eight-coordinate while the Cr3+ ions in the anionic complex are six-coordinate in a distorted octahedral geometry. Coulombic interactions between the ionic motifs and the three-dimensional H-bonding involving aqua ligands help to consolidate the bulk structure. Thermogra-vimetric analysis (TGA) shows that compound 1 is stable to heat up to ca. 80℃.展开更多
Reaction of Ba(NO3)2 with Fe(NO3)3·9H2O and H2C2O4·2H2O in aqueous medium readily affords, in high yield, the bimetallic complex polymer of chemical composition {Ba6(H2O)17[Fe(C2O4)3]4}·7H2O (1), consis...Reaction of Ba(NO3)2 with Fe(NO3)3·9H2O and H2C2O4·2H2O in aqueous medium readily affords, in high yield, the bimetallic complex polymer of chemical composition {Ba6(H2O)17[Fe(C2O4)3]4}·7H2O (1), consistent with the expected ratio of 3BaII vs. 2FeIII. Compound 1 was fully characterized by elemental and thermal analyses, vibrational FTIR spectroscopy, and by single crystal X-ray structure determination. The bulk structure of 1 is a 3-D metal-organic framework held together by intermetallic linkages across oxalate and aqua oxygen bridgings. Thermal analyses of 1 show significant weight losses corresponding to water molecules (lattice and coordinated), followed by the decomposition of the network.展开更多
文摘A new compound of general formula {[(H2O)2K(μ-H2O)Sr]@[Cr(C2O4)3]}n (1) has been synthesized in water and characterized by elemental and thermal analyses, EDX, IR and UV-Vis spectroscopies and by single crystal X-ray structure determination. Compound 1 crystallizes in the chiral space group Fdd2 of orthorhombic system with a = 14.110 (4) ?, b = 36.074 (11)?, c =11.034 (3)? and Z = 16. Compound 1 is a coordination polymer in which the three-dimensional lattice framework is realized by the interconnectivity between K+ cations, Sr2+ cations, aqua ligands and [Cr(C2O4)3]3– complex anions. The asymmetric unit of 1 consists of one cationic motif formally written [(H2O)2K(μ-H2O)Sr]3+ and one anionic entity, [Cr(C2O4)3]3–. The K+ and Sr2+ ions in the cationic motif are both eight-coordinate while the Cr3+ ions in the anionic complex are six-coordinate in a distorted octahedral geometry. Coulombic interactions between the ionic motifs and the three-dimensional H-bonding involving aqua ligands help to consolidate the bulk structure. Thermogra-vimetric analysis (TGA) shows that compound 1 is stable to heat up to ca. 80℃.
文摘Reaction of Ba(NO3)2 with Fe(NO3)3·9H2O and H2C2O4·2H2O in aqueous medium readily affords, in high yield, the bimetallic complex polymer of chemical composition {Ba6(H2O)17[Fe(C2O4)3]4}·7H2O (1), consistent with the expected ratio of 3BaII vs. 2FeIII. Compound 1 was fully characterized by elemental and thermal analyses, vibrational FTIR spectroscopy, and by single crystal X-ray structure determination. The bulk structure of 1 is a 3-D metal-organic framework held together by intermetallic linkages across oxalate and aqua oxygen bridgings. Thermal analyses of 1 show significant weight losses corresponding to water molecules (lattice and coordinated), followed by the decomposition of the network.
