Morphology design and control of a novel 3D potassium metal-organic coordination polymer compound: Crystallography, DFT, thermal, and biological studies

2020 ◽  
pp. 129434
Author(s):  
Maryam Aghaee ◽  
Khosro Mohammadi ◽  
Payam Hayati ◽  
Sara Ahmadi ◽  
Fatemeh Yazdian ◽  
...  
2019 ◽  
Vol 1176 ◽  
pp. 434-446 ◽  
Author(s):  
Mohammad Kazem Mohammadi ◽  
Payam Hayati ◽  
Samira Jafari ◽  
Mehdi Karimi ◽  
Angel Gutierrez

2016 ◽  
Vol 72 (11) ◽  
pp. 895-900
Author(s):  
Xin-Hua Lu ◽  
Kai-Long Zhong

The self-assembly of coordination polymers and the crystal engineering of metal–organic coordination frameworks have attracted great interest, but it is still a challenge to predict and control the compositions and structures of the complexes. Employing multidentate organic ligands and suitable metal ions to construct inorganic–organic hybrid materials through metal–ligand coordination and hydrogen-bonding interactions has become a major strategy. Recently, imidazole-containing multidentate ligands that contain an aromatic core have received much attention. A new three-dimensional MnIIcoordination polymer based on 1,3,5-tris[(1H-imidazol-1-yl)methyl]benzene, namely poly[(ethane-1,2-diol-κO)(μ-sulfato-κ2O:O′){μ3-1,3,5-tris[(1H-imidazol-1-yl)methyl]benzene-κ3N:N′:N′′}manganese(II)], [Mn(SO4)(C18H18N6)(C2H6O2)]n, was synthesized and characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. Crystal structural analysis shows that there are two kinds of crystallographically independent MnIIcentres, each lying on a centrosymmetric position and having a similar six-coordinated octahedral structure. One is coordinated by four N atoms from four 1,3,5-tris[(1H-imidazol-1-yl)methyl]benzene (timb) ligands and two O atoms from two different bridging sulfate anions. The second is surrounded by two timb N atoms and four O atoms, two from sulfate anions and two from two ethane-1,2-diol ligands. The tripodal timb ligand bridges neighbouring MnIIcentres to generate a two-dimensional layered structure running parallel to theabplane. Adjacent layers are further bridged by sulfate anions, resulting in a three-dimensional structure with3,4,6-ctopology. Thermogravimetric analysis of the title polymer shows that it is stable up to 533 K. The first weight loss between 533 and 573 K corresponds to the release of coordinated ethane-1,2-diol molecules, and further decomposition occurred at 648 K.


2018 ◽  
Author(s):  
Dominic Bara ◽  
Claire Wilson ◽  
Max Mörtel ◽  
Marat M. Khusniyarov ◽  
ben slater ◽  
...  

Phase control in the self-assembly of metal-organic frameworks (MOFs) – materials wherein organic ligands connect metal ions or clusters into network solids with potential porosity – is often a case of trial and error. Judicious control over a number of synthetic variables is required to select for the desired topology and control features such as interpenetration and defectivity, which have significant impact on physical properties and application. Herein, we present a comprehensive investigation of self-assembly in the Fe-biphenyl-4,4'-dicarboxylate system, demonstrating that coordination modulation, the addition of competing ligands into solvothermal syntheses, can reliably tune between the kinetic product, non-interpenetrated MIL-88D(Fe), and the thermodynamic product, two-fold interpenetrated MIL-126(Fe). DFT simulations reveal that correlated disorder of the terminal anions on the metal clusters in the interpentrated phase results in H-bonding between adjacent nets and is the thermodynamic driving force for its formation. Coordination modulation slows self-assembly and therefore selects the thermodynamic product MIL-126(Fe), while offering fine control over defectivity, inducing mesoporosity, but electron microscopy shows the MIL-88D(Fe) phase persists in many samples despite not being evident in diffraction experiments, suggesting its presence accounts for the lower than predicted surface areas reported for samples to date. Interpenetration control is also demonstrated by utilizing the 2,2'-bipyridine-5,5'-dicarboxylate linker; DFT simulations show that it is energetically prohibitive for it to adopt the twisted conformation required to form the interpenetrated phase, and are confirmed by experimental data, although multiple alternative phases are identified due to additional coordination of the Fe cations to the N-donors of the ligand. Finally, we introduce oxidation modulation – the concept of using metal precursors in a different oxidation state to that found in the final MOF – as a further protocol to kinetically control self-assembly. Combining coordination and oxidation modulation allows the synthesis of pristine MIL-126(Fe) with BET surface areas close to the predicted maximum capacity for the first time, suggesting that combining the two may be a powerful methodology for the controlled self-assembly of high-valent MOFs.<br><br>


Polyhedron ◽  
2021 ◽  
Vol 195 ◽  
pp. 114982
Author(s):  
Jun-Jie Lv ◽  
Feng-Lin Cao ◽  
Mei-Ling Wang ◽  
Xi-Mei Zong ◽  
Xiao-Min Kang ◽  
...  

2017 ◽  
Vol 349 ◽  
pp. 169-197 ◽  
Author(s):  
Jianwei Ren ◽  
Mpho Ledwaba ◽  
Nicholas M. Musyoka ◽  
Henrietta W. Langmi ◽  
Mkhulu Mathe ◽  
...  

Cells ◽  
2020 ◽  
Vol 9 (6) ◽  
pp. 1440 ◽  
Author(s):  
Weikang Nicholas Lin ◽  
Matthew Zirui Tay ◽  
Ri Lu ◽  
Yi Liu ◽  
Chia-Hung Chen ◽  
...  

The advent of single-cell research in the recent decade has allowed biological studies at an unprecedented resolution and scale. In particular, single-cell analysis techniques such as Next-Generation Sequencing (NGS) and Fluorescence-Activated Cell Sorting (FACS) have helped show substantial links between cellular heterogeneity and infectious disease progression. The extensive characterization of genomic and phenotypic biomarkers, in addition to host–pathogen interactions at the single-cell level, has resulted in the discovery of previously unknown infection mechanisms as well as potential treatment options. In this article, we review the various single-cell technologies and their applications in the ongoing fight against infectious diseases, as well as discuss the potential opportunities for future development.


2019 ◽  
Vol 74 (4) ◽  
pp. 341-345
Author(s):  
Kai-Long Zhong ◽  
Wei Song ◽  
Chao Ni ◽  
Guo-Qing Cao

AbstractA new coordination polymer [Cd(C10H8N2)2 (C10H4O8)]n (C10H8N2 = 2,2′-bipyridine and C10H4O8 = 2,5-dicarboxybenzene-1,4-dicarboxylate) has been hydrothermally synthesized and characterized by elemental analysis, infrared spectroscopy, thermal gravimetric analysis and single-crystal X-ray diffraction. Crystal structural analysis reveals that the CdII cation is coordinated by two 2,5-dicarboxybenzene-1,4-dicarboxylate ligands and two 2,2′-bipyridine molecules, forming a distorted octahedral CdN4O2 coordination geometry. The 2,5-dicarboxybenzene-1,4-dicarboxylate ligands link the CdII cations to generate a one-dimensional metal-organic structure running along the [0 1 0] direction. Adjacent chains are further connected by carboxyl-carboxyl O–H···O hydrogen bonds, resulting in a two-dimensional supermolecular architecture running parallel to the (1 0 0) plane in the solid state. The fluorescence properties of the complex were investigated.


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