Lanthanide-based F-MOFs: Structure, hydrolytic stability, spectral and magnetic properties

IF 3.2 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Journal of Solid State Chemistry Pub Date : 2024-08-08 DOI:10.1016/j.jssc.2024.124949
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Abstract

A series of five novel lanthanide-based fluorinated metal-organic frameworks (Ln-F-MOFs) have been synthesized under solvothermal conditions by the reaction of 3,3′-bis(trifluoromethyl)-[1,1′-biphenyl]-4,4′-dicarboxylic acid (H2L) and lanthanide Ln(III) ions (Ln(III)La, Ce, Pr, Nd and Eu). Powder X-ray diffraction (PXRD) analysis revealed that all prepared complexes are isostructural. A single-crystal X-ray crystallographic study of one representative of the isostructural group, namely {[La2(L)3(DMF)2(H2O)2]}n showed, that compound crystallizes in a triclinic system with space group P-1. The lattice parameter values are a = 8.563(2) Å, b = 13.199(3) Å, c = 16.008(4) Å, α = 104.588(7) °, β = 92.904(7) ° and γ = 92.717(7) °, with two formula units in the unit cell. The overall structure is formed by 2D polymeric layers, which are arranged into a semi-3D supramolecular structure through hydrogen bonds and other intramolecular interactions. The study of the hydrophobic properties of the complexes showed that the complexes exhibit surface hydrophobicity with a “rose petal effect” and a contact angle of approximately 107°. However, the structures are not hydrolytically stable in the long term and the structure starts to delaminate after two days in water. This is a manifestation of the fact that the complexes do not form a 3D polymer network, it is made up of 2D layers connected only by weak non-bonding interactions. The photoluminescence properties of the Ln(III) complexes are determined by the characteristic 5d-4f or 4f-4f electron transitions for the individual lanthanide ions. The magnetic properties of Nd(III), Pr(III) and Eu(III) variants were studied. The magnetic properties of {[Pr2(L)3(DMF)2(H2O)2]}n are characterized by the presence of a low-lying quasi-doublet with 15.6 cm−1 energy splitting, whereas Eu(III) variant is nonmagnetic at low temperatures, but the magnetic 7F1 state is accessible by thermal excitation. For Nd(III) complex, the X-band EPR measurements were performed. Since 1D channels with dimensions of 4.90 × 7.23 Å2 are present within the structure, the adsorption of N2, CO2 and H2 gases was also studied.

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基于镧系元素的 F-MOF:结构、水解稳定性、光谱和磁性能
通过 3,3′-双(三氟甲基)-[1,1′-联苯]-4,4′-二羧酸(H2L)和镧系镧(III)离子(Ln(III)La、Ce、Pr、Nd 和 Eu)反应,在溶热条件下合成了一系列五种新型镧系氟化金属有机框架(Ln-F-MOFs)。粉末 X 射线衍射(PXRD)分析表明,所有制备的配合物都是等结构的。对等结构组中的一个代表,即{[La2(L)3(DMF)2(H2O)2]}n进行的单晶 X 射线晶体学研究表明,该化合物在空间群为 P-1 的三菱系中结晶。晶格参数值为 a = 8.563(2)埃,b = 13.199(3)埃,c = 16.008(4)埃,α = 104.588(7)°,β = 92.904(7)°,γ = 92.717(7)°,单位晶胞中有两个公式单元。整体结构由二维聚合物层构成,这些聚合物层通过氢键和其他分子内相互作用排列成半三维超分子结构。对复合物疏水性的研究表明,复合物具有表面疏水性,具有 "玫瑰花瓣效应",接触角约为 107°。然而,这种结构并不具有长期的水解稳定性,在水中浸泡两天后就会开始分层。这表明这些复合物并没有形成三维聚合物网络,而是由仅通过微弱的非键相互作用连接的二维层组成。镧(III)配合物的光致发光特性是由单个镧系离子的特征性 5d-4f 或 4f-4f 电子跃迁决定的。研究了 Nd(III)、Pr(III) 和 Eu(III) 变体的磁性能。{[Pr2(L)3(DMF)2(H2O)2]}n的磁性特征是存在一个低洼的准双态,能量分裂为15.6 cm-1,而Eu(III)变体在低温下无磁性,但通过热激发可以获得磁性7F1态。对 Nd(III)复合物进行了 X 波段 EPR 测量。由于结构中存在尺寸为 4.90 × 7.23 Å2 的一维通道,因此还对 N2、CO2 和 H2 气体的吸附进行了研究。
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来源期刊
Journal of Solid State Chemistry
Journal of Solid State Chemistry 化学-无机化学与核化学
CiteScore
6.00
自引率
9.10%
发文量
848
审稿时长
25 days
期刊介绍: Covering major developments in the field of solid state chemistry and related areas such as ceramics and amorphous materials, the Journal of Solid State Chemistry features studies of chemical, structural, thermodynamic, electronic, magnetic, and optical properties and processes in solids.
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