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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >HYDROTHERMAL SYNTHESES AND CRYSTAL STRUCTURES OF TWO OXOVANADIUM-ORGANODIPHOSPHONATE PHASES - [H2N(C2H4)(2)NH2][(VO)(2)(O3PCH2CH2CH2PO3H)(2)], A STAIR-STEP STRUCTURE INCORPORATING AN ORGANIC CATIONIC TEMPLATE, AND [(VO)(H2O)(O3PCH2NH(C2H4)(2)NHCH2PO3
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HYDROTHERMAL SYNTHESES AND CRYSTAL STRUCTURES OF TWO OXOVANADIUM-ORGANODIPHOSPHONATE PHASES - [H2N(C2H4)(2)NH2][(VO)(2)(O3PCH2CH2CH2PO3H)(2)], A STAIR-STEP STRUCTURE INCORPORATING AN ORGANIC CATIONIC TEMPLATE, AND [(VO)(H2O)(O3PCH2NH(C2H4)(2)NHCH2PO3

机译:[H2N(C2H4)(2)NH2] [(VO)(2)(O3PCH2CH2CH2PO3H)(2)],阶梯形结构和温度的水热合成和晶体结构(VO)(水)(O3PCH2NH(C2H4)(2)NHCH2PO3

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摘要

Two new members of the oxovanadium-organodiphosphonate system, V-O-R(PO3)(2)(4-), have been synthesized by hydrothermal methods and structurally characterized. The reaction of VCl4, propylenediphosphonic acid, piperazine, and H2O in the mole ratio 1:1.5:3:945 at 200 degrees C and 96 h yields [H2N(C2H4)(2)NH2][(VO)(2)(O3PCH2CH2CH2PO3H)(2)] (1), as green rodlike crystals. The structure consists of ribbons of corner-sharing vanadium square pyramids and phosphorus tetrahedra interconnected by the diphosphonate organic backbone into a stair-step structural motif. The reaction of VCl4, N,N-piperazinebis(methylenephosphonic acid), and H2O in the mole ratio 1:0.8:570 at 125 degrees C for 134 h yields [(VO)(H2O){O3PCH2NH(C2H4)(2)NHCH2PO3}] (2), as light aqua green crystals of cubic habit. The structure of 2 consists of inorganic V/P/O layers linked through the organodiphosphonate backbone into an array of alternating inorganic and organic layers. In contrast to those in 1, the vanadium sites are six-coordinate and the V/P/O layer structure is a defected form of the V-P-O ribbon of 1 with alternate vanadium sites vacant, Compound 1 exhibits magnetic properties consistent with antiferromagnetic coupling of the V(IV) sites, with J/k = -10.3 K as an estimate of the strength of the exchange. Crystal data: C10H26N2O14P4V2 (1), triclinic P (1) over bar, a = 6.244(1) Angstrom, b = 8.687(2) Angstrom, c = 11.156(2) Angstrom, alpha = 88.92(3)degrees, beta = 74.63(3)degrees, gamma = 74.32(3)degrees, V = 560.8(3) Angstrom(3), Z = D-calc = 1,842 g cm(-3), with structure solution and refinement based on 1663 reflections converging at R = 0.0662; C6H12N2O8P2V (2), monoclinic P2(1)/c, a = 7.999(2) Angstrom, b = 8.009(2) Angstrom, c = 9.201(2) Angstrom, beta = 100.24(3)degrees, V = 580.1(3) Angstrom(3), Z = 2, D-calc = 2.021 g cm(-3), 1453 reflections, R = 0.0593. [References: 37]
机译:氧钒-有机二膦酸酯系统的两个新成员,V-O-R(PO3)(2)(4-),已通过水热法合成并进行了结构表征。 VCl4,丙烯二膦酸,哌嗪和H2O在200℃和96小时的摩尔比为1:1.5:3:945的反应生成[H2N(C2H4)(2)NH2] [(VO)(2)(O3PCH2CH2CH2PO3H )(2)](1),为绿色棒状晶体。该结构由角共享钒方棱锥和四面体磷(由四膦酸盐有机骨架相互连接)组成的阶梯状结构图案组成。 VCl4,N,N-哌嗪双(亚甲基膦酸)和H2O在125摄氏度下以1:0.8:570的摩尔比反应134小时产生[(VO)(H2O){O3PCH2NH(C2H4)(2)NHCH2PO3 }](2),为淡绿色立方习惯的浅绿色晶体。 2的结构由无机V / P / O层组成,这些层通过有机二膦酸酯骨架连接成交替排列的无机层和有机层。与1中的钒形成对比,钒的位点为六坐标,V / P / O层结构是1的VPO带的缺陷形式,交替存在钒位,化合物1的磁性与反铁磁耦合相一致。 V(IV)站点,J / k = -10.3 K作为交换强度的估计。晶体数据:C10H26N2O14P4V2(1),斜线P(1)大于bar,a = 6.244(1)埃,b = 8.687(2)埃,c = 11.156(2)埃,alpha = 88.92(3)度,beta = 74.63(3)度,gamma = 74.32(3)度,V = 560.8(3)埃(3),Z = D-calc = 1,842 g cm(-3),基于1663年反射的结构解和细化在R = 0.0662; C6H12N2O8P2V(2),单斜晶P2(1)/ c,a = 7.999(2)埃,b = 8.009(2)埃,c = 9.201(2)埃,beta = 100.24(3)度,V = 580.1(3) )Angstrom(3),Z = 2,D-calc = 2.021 g cm(-3),1453反射,R = 0.0593。 [参考:37]

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