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Solvothermal synthesis of new metal organic framework structures in the zinc-terephthalic acid-dimethyl formamide system

机译:锌-对苯二甲酸-二甲基甲酰胺体系中溶剂热合成新的金属有机骨架结构

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Two new metal organic framework (MOF) structures have been obtained from the Zn-terephthalic acid (H2BDC)-dimethyl formamide (DMF) system and examined by single-crystal X-ray diffraction: Zn(C8H4O4)(C3H7NO), 1, monoclinic C2/m, a = 11.1369(5), b = 14.0217(7), c = 7.9890(4) angstrom, beta = 106.316(1)degrees, V = 1197.3(1) angstrom(3), T = 180(2) K, Z = 4, R-1 = 0.060, wR(2) = 0.169, S = 1.27; Zn(HCO2)(3)(C2H8N), 2, trigonal R (3) over barc, a = 8.1818(1), c = 22.1235(7) angstrom, V = 1282.57(5) angstrom(3), T = 180(2) K, Z = 6, R-1 = 0.014, wR(2) = 0.039, S = 1.11. Contrary to previously published structures in the same system, the crystals were obtained by solvothermal synthesis at 381 K. Structure 1 consists of 2-D layers stacked in an offset manner to accommodate DMF moieties coordinated to Zn2+ within voids in adjacent layers. Structure 2 consists of a 3-D network constructed from Zn2+ ions bridged by deprotonated formic acid moieties. Over time, the structure of 1 rearranges to Zn(C8H4O4)(C3H7NO)(H2O) [monoclinic P2(1), a = 6.6456(2), b = 15.2232(5), c = 12.6148(4) angstrom, beta = 104.110(2)degrees, V = 1237.70(7) angstrom(3), T = 100(2) K, Z = 4, R-1 = 0.048, wR(2) = 0.100, S = 1.07], which is identical to the known MOF-2 structure, obtained by crystallization at ambient conditions. The three structures were determined from crystals with similar crystal habits picked from a single solvothermal synthesis batch. The study demonstrates that MOF syntheses can give not only multiple crystal structures under different conditions, but also that numerous different structures, including some that are metastable, can be formed under identical conditions. (c) 2005 Elsevier Inc. All rights reserved.
机译:从对苯二甲酸锌(H2BDC)-二甲基甲酰胺(DMF)系统获得了两个新的金属有机骨架(MOF)结构,并通过单晶X射线衍射对其进行了检验:Zn(C8H4O4)(C3H7NO),1,单斜晶C2 / m,a = 11.1369(5),b = 14.0217(7),c = 7.9890(4)埃,beta = 106.316(1)度,V = 1197.3(1)埃(3),T = 180(2) )K,Z = 4,R-1 = 0.060,wR(2)= 0.169,S = 1.27; Zn(HCO2)(3)(C2H8N),2,barc上的三角R(3),a = 8.1818(1),c = 22.1235(7)埃,V = 1282.57(5)埃(3),T = 180 (2)K,Z = 6,R-1 = 0.014,wR(2)= 0.039,S = 1.11。与以前在同一系统中发布的结构相反,晶体是通过在381 K溶剂热合成获得的。结构1由以偏移方式堆叠的2-D层组成,以容纳与Zn2 +配位的DMF部分在相邻层的空隙中。结构2由3-D网络组成,该网络由由去质子化的甲酸部分桥接的Zn2 +离子构成。随着时间的流逝,1的结构重新排列为Zn(C8H4O4)(C3H7NO)(H2O)[单斜晶P2(1)/ n,a = 6.6456(2),b = 15.2232(5),c = 12.6148(4)埃, β= 104.110(2)度,V = 1237.70(7)埃(3),T = 100(2)K,Z = 4,R-1 = 0.048,wR(2)= 0.100,S = 1.07],与在环境条件下结晶获得的已知MOF-2结构相同。从单个溶剂热合成批次中选取具有相似晶体习性的晶体确定这三个结构。研究表明,MOF合成不仅可以在不同条件下提供多种晶体结构,而且可以在相同条件下形成许多不同的结构,包括亚稳结构。 (c)2005 Elsevier Inc.保留所有权利。

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