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具有四种磁基态和气体吸附变化的纳米多孔钴(II) MOF 后合成修饰。

Nanoporous cobalt(II) MOF exhibiting four magnetic ground states and changes in gas sorption upon post-synthetic modification.

机构信息

Department of Chemistry and Pharmaceutical Sciences, Guangxi Normal University , Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education), Guilin, 541004, P. R. China.

出版信息

J Am Chem Soc. 2014 Mar 26;136(12):4680-8. doi: 10.1021/ja500191r. Epub 2014 Mar 17.

Abstract

We present the syntheses, structural characterization, gas sorption, I2 uptake, and magnetic properties of a double-walled porous metal-organic framework, [Co(II)3(lac)2(pybz)2]·3DMF (1·3DMF, purple, where pybz = 4-pyridyl benzoate, lac = d- and l-lactate) and of its post-synthetic modified (PSM) congeners, [Co(II)3(lac)2(pybz)2]·xGuest (xGuest = 6MeOH, purple; 4.5EtOH, purple; 3PrOH, purple; 2C6H6, purple; 2.7I2, black), [Co(II)3(lac)2(pybz)2] (1, purple), [Co(II)3(pybz)2(lac)2(H2O)2]·7H2O (1a·7H2O, green), and [Co(III)Co(II)2(pybz)2(lac)2(H2O)2]I·2H2O·1.5DMSO (1b·I(-)·2H2O·1.5DMSO, yellow, DMSO = dimethyl sulfoxide). Crystallography shows that the framework is not altered by the replacement of DMF by different solvents or by the removal of the solvent molecules during the single-crystal to single-crystal (SC-SC) transformations, while upon exchange with H2O or partial oxidation by molecular iodine, the crystallinity is affected. 1 absorbs N2, H2, CH4, CH3OH, C2H5OH, PrOH, C6H6, and I2, but once it is in contact with H2O the absorption efficiency is drastically reduced. Upon PSM, the magnetism is transformed from a canted antiferromagnet (1·3DMF and 1·xGuest) to single-chain magnet (1), to a ferrimagnet (1a·7H2O), and to a ferromagnet (1b·I(-)·2H2O·1.5DMSO). Raman spectroscopy suggests the color change (purple to green 1a·7H2O or yellow 1b·I(-)·2H2O·1.5DMSO) is associated with a change of geometry from a strained octahedron due to the very acute chelating angle (∼60°) of the lactate of a cobalt center to a regular octahedron with a monodentate carboxylate and one H2O. The magnetic transformation is explained by the different interchain exchanges (J'), antiferromagnetic for 1·3DMF and 1·xSolvent (J' < 0), SCM for 1 (J' verge to 0), and ferromagnetic for 1a·7H2O (J' > 0), between homometal topological ferrimagnetic chains (two octahedral and one tetrahedral Co(II) ions) connected by the double walls of pybz at 13.3 Å (shortest Co···Co). For 1b·I(-)·2H2O·1.5DMSO the moment of the tetrahedral site is turned off, thus stabilizing a ferromagnetic state (J' > 0). The present stabilization of four magnetic ground states is unique in the field of metal-organic frameworks as well as the electrical conductivity of 1·2.7I2.

摘要

我们展示了一种双壁多孔金属有机骨架[Co(II)3(lac)2(pybz)2]·3DMF(1·3DMF,紫色,其中 pybz = 4-吡啶基苯甲酸酯,lac = d-和 l-乳酸)及其后合成修饰(PSM)同系物[Co(II)3(lac)2(pybz)2]·xGuest(xGuest = 6MeOH,紫色;4.5EtOH,紫色;3PrOH,紫色;2C6H6,紫色;2.7I2,黑色)、[Co(II)3(lac)2(pybz)2](1,紫色)、[Co(II)3(pybz)2(lac)2(H2O)2]·7H2O(1a·7H2O,绿色)和[Co(III)Co(II)2(pybz)2(lac)2(H2O)2]I·2H2O·1.5DMSO(1b·I(-)·2H2O·1.5DMSO,黄色,DMSO = 二甲基亚砜)的合成、结构特征、气体吸附、I2 摄取和磁性能。晶体学表明,在单晶到单晶(SC-SC)转变过程中,框架不会因 DMF 被不同溶剂替代或溶剂分子的去除而改变,而在与 H2O 交换或分子碘部分氧化时,结晶度会受到影响。1 吸收 N2、H2、CH4、CH3OH、C2H5OH、PrOH、C6H6 和 I2,但一旦与 H2O 接触,吸收效率就会大幅降低。经过 PSM,磁性从倾斜反铁磁(1·3DMF 和 1·xGuest)转变为单链磁体(1)、亚铁磁体(1a·7H2O)和铁磁体(1b·I(-)·2H2O·1.5DMSO)。拉曼光谱表明,颜色变化(从紫色变为绿色 1a·7H2O 或黄色 1b·I(-)·2H2O·1.5DMSO)与几何形状的变化有关,由于钴中心的乳酸的非常锐角螯合角(约 60°),从应变八面体变为具有单齿羧酸盐和一个 H2O 的规则八面体。磁性转变可以通过不同的链间交换(J')来解释,对于 1·3DMF 和 1·xSolvent(J' < 0)为反铁磁,对于 1(J'趋于 0)为单链磁体,对于 1a·7H2O(J' > 0)为铁磁,在由 pybz 连接的同金属拓扑亚铁磁链(两个八面体和一个四面体 Co(II)离子)之间进行,间隔为 13.3 Å(最短的 Co···Co)。对于 1b·I(-)·2H2O·1.5DMSO,四面体位置的磁矩被关闭,从而稳定了铁磁状态(J' > 0)。目前,在金属有机骨架领域以及 1·2.7I2 的电导率方面,四种磁基态的稳定是独一无二的。

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