Exploring conformationally flexible hydrogen-bond-functionalized ligand and counter anions in metal–organic frameworks of Cu(ii)

2006 ◽  
Vol 30 (9) ◽  
pp. 1267-1275 ◽  
Author(s):  
D. Krishna Kumar ◽  
Amitava Das ◽  
Parthasarathi Dastidar
Keyword(s):  
Hydrogen Bond ◽  
Metal Organic Frameworks ◽  
Metal Organic

Identifying Selective Host–Guest Interactions Based on Hydrogen Bond Donor–Acceptor Pattern in Functionalized Al-MIL-53 Metal–Organic Frameworks

2013 ◽  
Vol 117 (39) ◽  
pp. 19991-20001 ◽  
Author(s):  
Julia Wack ◽  
Renée Siegel ◽  
Tim Ahnfeldt ◽  
Norbert Stock ◽  
Luís Mafra ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Metal Organic Frameworks ◽  
Hydrogen Bond Donor ◽  
Donor Acceptor ◽  
Metal Organic

Selective adsorption behaviour of carbon dioxide in OH-functionalized metal–organic framework materials

CrystEngComm ◽  
2017 ◽  
Vol 19 (36) ◽  
pp. 5346-5350 ◽  
Author(s):  
Jinjie Qian ◽  
Jinni Shen ◽  
Qipeng Li ◽  
Yue Hu ◽  
Shaoming Huang
Keyword(s):  
Carbon Dioxide ◽  
Hydrogen Bond ◽  
Selective Adsorption ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Adsorption Behaviour ◽  
Weak Hydrogen Bond ◽  
Oh Groups ◽  
Framework Materials ◽  
Metal Organic

The theoretically optimal adsorption locations in hydroxyl (OH)-decorated metal–organic frameworks show that the captured CO2 molecules interact with the cis-μ2-OH groups in an end-on mode, which shows a moderate to weak hydrogen bond.

Hydrogen Bond Tuning of Magnetoelectric Coupling in Metal–Organic Frameworks

2020 ◽  
Vol 124 (29) ◽  
pp. 16111-16115 ◽  
Author(s):  
Chao Liu ◽  
Kun Zhai ◽  
Zhipeng Yu ◽  
Anmin Nie ◽  
Zhongyuan Liu ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Metal Organic Frameworks ◽  
Magnetoelectric Coupling ◽  
Metal Organic

Intramolecular hydrogen bond-induced high chemical stability of metal–organic frameworks

2020 ◽  
Vol 7 (19) ◽  
pp. 3548-3554
Author(s):  
Keke Wang ◽  
Qunmin Wang ◽  
Xiong Wang ◽  
Mei Wang ◽  
Qin Wang ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonds ◽  
Intramolecular Hydrogen Bond ◽  
Chemical Stability ◽  
Metal Organic Frameworks ◽  
Carboxyl Groups ◽  
High Chemical ◽  
Metal Organic ◽  
Intramolecular Hydrogen ◽  
High Chemical Stability

Intramolecular hydrogen bonds in ligands restrict the rotation of carboxyl groups and consequently enhance the chemical stability of MOFs.

Structural variation of transition metal–organic frameworks using deep eutectic solvents with different hydrogen bond donors

2019 ◽  
Vol 48 (27) ◽  
pp. 10199-10209 ◽  
Author(s):  
Ming-Yu Zhao ◽  
Jian-Nan Zhu ◽  
Peng Li ◽  
Wei Li ◽  
Ting Cai ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Transition Metal ◽  
Structural Variation ◽  
Metal Organic Frameworks ◽  
Three Dimensional ◽  
Deep Eutectic Solvents ◽  
One Dimensional ◽  
Metal Organic ◽  
Hydrogen Bond Donors

Seven transition metal–organic frameworks with structures ranging from one-dimensional chains to three-dimensional networks have been synthesized in deep eutectic solvents.

Selective host–guest interactions in metal–organic frameworks via multiple hydrogen bond donor–acceptor recognition sites

2019 ◽  
Vol 7 (17) ◽  
pp. 10379-10388 ◽  
Author(s):  
T. Wittmann ◽  
C. B. L. Tschense ◽  
L. Zappe ◽  
C. Koschnick ◽  
R. Siegel ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Hydrogen Bond ◽  
Porous Materials ◽  
Metal Organic Frameworks ◽  
Hydrogen Bond Donor ◽  
Recognition Sites ◽  
Molecular Separation ◽  
Multiple Hydrogen Bond ◽  
Donor Acceptor ◽  
Metal Organic

Targeted recognition of medium sized molecules with mixed hydrogen bond units is essential for using porous materials for molecular separation, sensing and drug delivery.

scholarly journals Structure-directing factors when introducing hydrogen bond functionality to metal–organic frameworks

CrystEngComm ◽  
2015 ◽  
Vol 17 (2) ◽  
pp. 299-306 ◽  
Author(s):  
Ross S. Forgan ◽  
Ross J. Marshall ◽  
Mona Struckmann ◽  
Aurore B. Bleine ◽  
De-Liang Long ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Functional Groups ◽  
Noncovalent Interactions ◽  
Metal Organic Frameworks ◽  
Metal Organic

Introduction of functional groups into an isoreticular series of MOFs may be complicated by noncovalent interactions between interpenetrated nets inducing differing topologies.

scholarly journals Metal-Organic Frameworks of MIL-100(Fe, Cr) and MIL-101(Cr) for Aromatic Amines Adsorption from Aqueous Solutions

Molecules ◽  
2019 ◽  
Vol 24 (20) ◽  
pp. 3718 ◽  
Author(s):  
Mao-Long Chen ◽  
Shu-Yang Zhou ◽  
Zhou Xu ◽  
Li Ding ◽  
Yun-Hui Cheng
Keyword(s):  
Hydrogen Bond ◽  
Electron Microscope ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Aromatic Amines ◽  
Intermolecular Hydrogen Bond ◽  
Metal Organic Frameworks ◽  
Hydrogen Bond Acceptor ◽  
Metal Organic ◽  
Cavity System

MIL-100(Fe, Cr) and MIL-101(Cr) were synthesized by the hydrothermal method and applied to the adsorptions of five aromatic amines from aqueous solutions. These three metal-organic frameworks (MOFs) were well characterized by powder X-ray diffraction (PXRD), scanning electron microscope (SEM), transmission electron microscope (TEM), thermogravimetric analysis (TGA) and surface area analysis. The adsorption mechanism of three MOFs and the effects of the structures of MOFs on the adsorption of aromatic amines were discussed. The results show that the cavity system and suitable hydrogen bond acceptor were important factors for the adsorption for five aromatic amines of aniline, 1-naphthalamine, o-toluidine, 2-amino-4-nitrotoluene and 2-nitroaniline: (a) the saturated adsorption capacity of aniline, 1-naphthylamine and o-toluidine on MIL-100(Fe) were 52.0, 53.4 and 49.6 mg/g, respectively, which can be attributed to the intermolecular hydrogen bond interaction and cavity system diffusion. (b) The adsorption capacity of 2-nitroaniline and 2-amino-4-nitrotoluene on MIL-101(Cr) were 54.3 and 25.0 mg/g, respectively, which can be attributed to the more suitable pore size of MIL-101(Cr) than that of MIL-100(Fe, Cr). The MOFs of MIL-100(Fe) and MIL-101(Cr) can be potential materials for removing aromatic amines from aqueous solutions.

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