Metal–organic frameworks with improved moisture stability based on a phosphonate monoester: effect of auxiliary N-donor ligands on framework dimensionality

CrystEngComm ◽  
2014 ◽  
Vol 16 (29) ◽  
pp. 6635-6644 ◽  
Author(s):  
Jian-Wei Zhang ◽  
Cui-Cui Zhao ◽  
Yin-Ping Zhao ◽  
Hai-Qun Xu ◽  
Zi-Yi Du ◽  
...  
Keyword(s):  
Metal Organic Frameworks ◽  
Donor Ligands ◽  
Metal Organic ◽  
Moisture Stability ◽  
1D Chains ◽  
3D Networks

A series of metal–organic frameworks (MOFs) with improved moisture stability based on a phosphonate monoester, featuring 1D chains, 2D layers and 3D networks, have been obtained in the presence of auxiliary N-donor ligands.

scholarly journals Highly sensitive detection of nitrobenzene by a series of fluorescent 2D zinc(ii) metal–organic frameworks with a flexible triangular ligand

RSC Advances ◽  
2021 ◽  
Vol 11 (39) ◽  
pp. 23975-23984
Author(s):  
Xue Yang ◽  
Yixia Ren ◽  
Hongmei Chai ◽  
Xiufang Hou ◽  
Zhixiang Wang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Metal Organic Frameworks ◽  
High Sensitivity ◽  
Fluorescent Sensors ◽  
Sensitive Detection ◽  
Donor Ligands ◽  
Highly Sensitive ◽  
Metal Organic ◽  
Highly Sensitive Detection

Four fluorescent 2D Zn-MOFs based on a flexible triangular ligand and linear N-donor ligands are hydrothermally prepared and used to detect nitrobenzene in aqueous solution with high sensitivity, demonstrating their potential as fluorescent sensors.

Syntheses and structures of two novel fluorescent metal–organic frameworks generated from a tridentate donor–acceptor motif ligand

2020 ◽  
Vol 76 (6) ◽  
pp. 605-615
Author(s):  
Yong-Jin Zhao ◽  
Jian-Ping Ma ◽  
Jianzhong Fan ◽  
Yan Geng ◽  
Yu-Bin Dong
Keyword(s):  
Solid State ◽  
Hydrogen Bonds ◽  
Weak Interactions ◽  
Metal Organic Frameworks ◽  
3D Structure ◽  
Organic Ligand ◽  
Bidentate Ligand ◽  
Donor Acceptor ◽  
Metal Organic ◽  
3D Networks

The tridentate organic ligand 4,4′,4′′-(4,4,8,8,12,12-hexamethyl-8,12-dihydro-4H-benzo[9,1]quinolizino[3,4,5,6,7-defg]acridine-2,6,10-triyl)tribenzoic acid (H3L) has been synthesized (as the methanol 1.25-solvate, C48H39NO6·1.25CH3OH). As a donor–acceptor motif molecule, H3L possess strong intramolecular charge transfer (ICT) fluorescence. Through hydrogen bonds, H3L molecules construct a two-dimensional (2D) network, which pack together into three-dimensional (3D) networks with an ABC stacking pattern in the crystalline state. Based on H3L and M(NO3)2 salts (M = Cd and Zn) under solvothermal conditions, two metal–organic frameworks (MOFs), namely, catena-poly[[triaquacadmium(II)]-μ-10-(4-carboxyphenyl)-4,4′-(4,4,8,8,12,12-hexamethyl-8,12-dihydro-4H-benzo[9,1]quinolizino[3,4,5,6,7-defg]acridine-2,6-diyl)dibenzoato], [Cd(C48H37NO6)(H2O)3] n , I, and poly[[μ3-4,4′,4′′-(4,4,8,8,12,12-hexamethyl-8,12-dihydro-4H-benzo[9,1]quinolizino[3,4,5,6,7-defg]acridine-2,6,10-triyl)tribenzoato](μ3-hydroxido)zinc(II)], [Zn2(C48H36NO6)(OH)] n , II, were synthesized. Single-crystal analysis revealed that both MOFs adopt a 3D structure. In I, partly deprotonated HL 2− behaves as a bidentate ligand to link a CdII ion to form a one-dimensional chain. In the solid state of I, the existence of weak interactions, such as O—H...O hydrogen bonds and π–π interactions, plays an essential role in aligning 2D nets and 3D networks with AB packing patterns for I. The deprotonated ligand L 3− in II is utilized as a tridentate building block to bind ZnII ions to construct 3D networks, where unusual Zn4O14 clusters act as connection nodes. As a donor–acceptor molecule, H3L exhibits fluorescence with a photoluminescence quantum yield (PLQY) of 70% in the solid state. In comparison, the PL of both MOFs is red-shifted with even higher PLQYs of 79 and 85% for I and II, respectively.

scholarly journals Increasing the Stability of Metal-Organic Frameworks

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Mathieu Bosch ◽  
Muwei Zhang ◽  
Hong-Cai Zhou
Keyword(s):  
Metal Organic Frameworks ◽  
Luminescent Properties ◽  
Vacuum Treatment ◽  
Donor Ligands ◽  
Gas Sorption ◽  
Nitrogen Donor Ligands ◽  
Metal Centers ◽  
Ligand Interactions ◽  
Metal Organic ◽  
The Stability

Metal-organic frameworks (MOFs) are a new category of advanced porous materials undergoing study by many researchers for their vast variety of both novel structures and potentially useful properties arising from them. Their high porosities, tunable structures, and convenient process of introducing both customizable functional groups and unsaturated metal centers have afforded excellent gas sorption and separation ability, catalytic activity, luminescent properties, and more. However, the robustness and reactivity of a given framework are largely dependent on its metal-ligand interactions, where the metal-containing clusters are often vulnerable to ligand substitution by water or other nucleophiles, meaning that the frameworks may collapse upon exposure even to moist air. Other frameworks may collapse upon thermal or vacuum treatment or simply over time. This instability limits the practical uses of many MOFs. In order to further enhance the stability of the framework, many different approaches, such as the utilization of high-valence metal ions or nitrogen-donor ligands, were recently investigated. This review details the efforts of both our research group and others to synthesize MOFs possessing drastically increased chemical and thermal stability, in addition to exemplary performance for catalysis, gas sorption, and separation.

Moisture stability of ethane‐selective Ni(II), Fe(III), Zr(IV)‐based metal–organic frameworks

AIChE Journal ◽  
2019 ◽  
Vol 65 (8) ◽  
Author(s):  
Daofei Lv ◽  
Jiayu Chen ◽  
Yongwei Chen ◽  
Zewei Liu ◽  
Yuzhi Xu ◽  
...  
Keyword(s):  
Metal Organic Frameworks ◽  
Metal Organic ◽  
Moisture Stability

Construction of hybrid d10 metal–organic frameworks by flexible aromatic dicarboxylate and N-donor ligands :  syntheses, structures and physical properties

CrystEngComm ◽  
2009 ◽  
Vol 11 (12) ◽  
pp. 2784 ◽  
Author(s):  
Guang-Xiang Liu ◽  
Kun Zhu ◽  
Huan-Min Xu ◽  
Sadafumi Nishihara ◽  
Rong-Yi Huang ◽  
...  
Keyword(s):  
Physical Properties ◽  
Metal Organic Frameworks ◽  
Donor Ligands ◽  
D10 Metal ◽  
Metal Organic

Lanthanide(III) complex metal-organic frameworks with a phenanthroline-carboxylate derivate and 2,5-thiophenedicarboxylate coligand: hydrothermal synthesis, crystal structure, and high thermostability

2018 ◽  
Vol 73 (5) ◽  
pp. 311-317
Author(s):  
Zhao Xu ◽  
Fengqin An ◽  
Xiaohui Ma ◽  
Huiliang Zhou ◽  
Weiming Song ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Thermal Stability ◽  
Metal Organic Frameworks ◽  
Decomposition Temperature ◽  
Thermal Decomposition Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metal Organic ◽  
3D Networks ◽  
Point Symbol

AbstractBased on 2-(4-carboxyphenyl)imidazo[4,5-f]-1,10-phenanthroline (HNCP) and 2,5-thiophenedicarboxylate (TDC2−) ligands, three new lanthanide-containing (Sm, Nd, and Pr) compounds, [Sm(NCP)(TDC)]n (1), [Nd(NCP)(TDC)]n·2n(H2O)0.5 (2), and [Pr(NCP)(TDC)]n·n(H2O)0.5 (3), have been synthesized using the hydrothermal method and structurally characterized using single-crystal X-ray diffraction. Structural analyses have revealed that compounds 1–3 are 3D isostructural metal-organic frameworks in which the [Ln2(COO)4] dimers can be regarded as 6-connecting nodes, and the TDC2− and NCP− ligands are simplified as connectors to achieve the double interspersed 3D networks with the point symbol {412·63}. Thermogravimetric analysis has illustrated that the rigid architecture contributes to superior thermal stability with a thermal decomposition temperature of more than 400°C for the resulting metal-organic frameworks.

Syntheses and Characterizations of Multidimensional Metal-Organic Frameworks Based on Rings and 1D Chains

2005 ◽  
Vol 2005 (2) ◽  
pp. 321-329 ◽  
Author(s):  
Xiaoju Li ◽  
Rong Cao ◽  
Yanqiong Sun ◽  
Wenhua Bi ◽  
Xing Li ◽  
...  
Keyword(s):  
Metal Organic Frameworks ◽  
Metal Organic ◽  
1D Chains
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