Two Metal–Organic Coordination Polymers Based on Polypyridyl Ligands: Crystal Structures and Inhibition of Human Spinal Tumour Cells

2018 ◽  
Vol 71 (11) ◽  
pp. 902
Author(s):  
Hua-Jie Mao ◽  
Qi-Xin Chen ◽  
Bin Han

In this work, two new metal–organic coordination polymers [Co2.5(dtp)2(H2O)5](NO3)(H2O)2 (1, H2dtp = 4′-(3,5-dicarboxyphenyl)-2,2′:6′,2″-terpyridine) [Ni(dpt)](H2O)3 (2, H2dpt = 4′-(3,5-dicarboxyphenyl)-4,2′:6′,4″- terpyridine) have been successfully prepared by reaction of metal ions with two similar carboxylic-pyridinyl ligands with different arrangement of N atoms of terpyridines under solvothermal conditions. Powder X-ray diffraction, elemental analysis, and single-crystal X-ray diffraction techniques were used to probe the structures of the as-prepared complexes. The CoII-based complex 1 exhibits a finite molecular structure and 2 displays a 3D porous framework with a 1D channel. Furthermore, the in vitro anticancer activity of complexes 1 and 2 was evaluated via the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay against U-266, MM1S, and RPMI-8226 human spinal tumour cells.

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 204
Author(s):  
Yu Li ◽  
Chumin Liang ◽  
Xunzhong Zou ◽  
Jinzhong Gu ◽  
Marina V. Kirillova ◽  
...  

Three 2D coordination polymers, [Cu2(µ4-dpa)(bipy)2(H2O)]n∙6nH2O (1), [Mn2(µ6-dpa)(bipy)2]n (2), and [Zn2(µ4-dpa)(bipy)2(H2O)2]n·2nH2O (3), were prepared by a hydrothermal method using metal(II) chloride salts, 3-(2′,4′-dicarboxylphenoxy)phthalic acid (H4dpa) as a linker, as well as 2,2′-bipyridine (bipy) as a crystallization mediator. Compounds 1–3 were obtained as crystalline solids and fully characterized. The structures of 1–3 were established by single-crystal X-ray diffraction, revealing 2D metal-organic networks of sql, 3,6L66, and hcb topological types. Thermal stability and catalytic behavior of 1–3 were also studied. In particular, zinc(II) coordination polymer 3 functions as a highly active and recoverable heterogeneous catalyst in the mild cyanosilylation of benzaldehydes with trimethylsilyl cyanide to give cyanohydrin derivatives. The influence of various parameters was investigated, including a time of reaction, a loading of catalyst and its recycling, an effect of solvent type, and a substrate scope. As a result, up to 93% product yields were attained in a catalyst recoverable and reusable system when exploring 4-nitrobenzaldehyde as a model substrate. This study contributes to widening the types of multifunctional polycarboxylic acid linkers for the design of novel coordination polymers with notable applications in heterogeneous catalysis.


2021 ◽  
Vol 47 (9) ◽  
pp. 593-600
Author(s):  
A. A. Lysova ◽  
V. A. Dubskikh ◽  
K. D. Abasheeva ◽  
A. A. Vasileva ◽  
D. G. Samsonenko ◽  
...  

Abstract Three new metal−organic frameworks based on scandium(III) cations and 2,5-thiophenedicarboxylic acid (H2Tdc) are synthesized: [Sc(Tdc)(OH)]·1.2DMF (I), [Sc(Tdc)(OH)]·2/3DMF (II), and (Me2NH2)[Sc3(Tdc)4(OH)2]·DMF (III) (DMF is N,N-dimethylformamide). The structures of the compounds are determined by single-crystal X-ray structure analysis (CIF file CCDC nos. 2067819 (I), 2067820 (II), and 2067821 (III)). The chemical and phase purity of compound I is proved by elemental analysis, thermogravimetry, X-ray diffraction analysis, and IR spectroscopy.


2015 ◽  
Vol 71 (7) ◽  
pp. 618-622 ◽  
Author(s):  
Shao-Ming Ying ◽  
Jing-Jing Ru ◽  
Wu-Kui Luo

Metal–organic frameworks (MOFs) have potentially useful applications and an intriguing variety of architectures and topologies. Two homochiral coordination polymers have been synthesized by the hydrothermal method, namely poly[(μ-N-benzyl-L-phenylalaninato-κ4O,O′:O,N)(μ-formato-κ2O:O′)zinc(II)], [Zn(C16H16NO2)(HCOO)]n, (1), and poly[(μ-N-benzyl-L-leucinato-κ4O,O′:O,N)(μ-formato-κ2O:O′)zinc(II)], [Zn(C13H18NO2)(HCOO)]n, (2), and studied by single-crystal X-ray diffraction, elemental analyses, IR spectroscopy and fluorescence spectroscopy. Compounds (1) and (2) each have a two-dimensional layer structure, with the benzyl or isobutyl groups of the ligands directed towards the interlayer interface. Photoluminescence investigations show that both (1) and (2) display a strong emission in the blue region.


2011 ◽  
Vol 66 (2) ◽  
pp. 125-132 ◽  
Author(s):  
Guo-Cheng Liu ◽  
Jin-Xia Zhang ◽  
Xiu-Li Wang ◽  
Hong-Yan Lin ◽  
Ai-Xiang Tian ◽  
...  

Three new Cd(II) metal-organic coordination polymers, [Cd(bbi)(DNBA)2] (1), [Cd(bbbi)- (DNBA)2] (2), and [Cd(dmbbbi)(DNBA)Cl]·0.38H2O (3) [HDNBA = 3,5-dinitrobenzoic acid, bbi = 1,1-(1,4-butanediyl)bis(imidazole), bbbi = 1,1-(1,4-butanediyl)bis(benzimidazole), and dmbbbi = 1,1-(1,4-butanediyl)bis(5,6-dimethylbenzimidazole)], have been obtained from hydrothermal reactions of cadmium(II) chloride with the mixed ligands HDNBA and the three structurally related flexible bis(imidazole) derivatives. Single-crystal X-ray diffraction analyses have revealed that the dinuclear cadmium clusters acting as nodes interlinked by two μ2-carboxylic groups, are connected to four other clusters through bridging bbi (for 1) and bbbi (for 2) units to generate two extended two-dimensional (2-D) networks. Compound 3 features a 1-D zigzag chain structure. A systematic structural comparison of the title compounds indicates that the conformations and the steric hindrance of flexible bis(imidazole) derivatives each play an important role in the formation of the Cd(II) coordination polymers. The thermal stability of 1 and 2, and the luminescence behavior of 3 were also investigated.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Li Tian ◽  
Zhi Long Ma ◽  
Mengchen Wang ◽  
Jian Yun Shi

Solvothermal reaction of a novel multidentate ligand 2,5-bis-(1,2,4-triazol-1-yl)-terephthalic acid (H2TTPA), with MnCl2 afforded three structurally different coordination polymers with the similar formula [Mn(TTPA)•H2O]n (Mn-(1-3)). Single-crystal X-ray diffraction analyses show that...


2018 ◽  
Vol 73 (12) ◽  
pp. 1023-1028
Author(s):  
Ying Zhang ◽  
Ai-Quan Jia ◽  
Jing-Jing Zhang ◽  
Zhifeng Xin ◽  
Qian-Feng Zhang

AbstractTwo coordination polymers, [Mn2(μ-O2PPh2)2(η1-O2PPh2)2(η1-HOCH3)2(μ-bpe)2·CH3OH]n (1) and [Mn2(μ-O2PPh2)4(μ-bpe)2]n (2), were assembled in single-pot reactions from [Mn(CH3COO)2·4H2O], Ph2P(O)OK and trans-1,4-bis(4-pyridyl)ethene (bpe). The products were characterized by single-crystal X-ray diffraction, which revealed a one-dimensional metal-organic ladder type in 1 and a two-dimensional rectangular grid type in 2. Both 1 and 2 are constructed from six-coordinate Mn(II) nodes that adopt distorted octahedral (MnN4O2) environments; the adjacent nodes are connected by the μ-bpe linkers in 1 or μ-bpe and μ-O2PPh2 linkers in 2 to form different metal-organic networks. The catalytic property of complex 1 for selective thioether oxidation was also investigated in this work.


1998 ◽  
Vol 5 (1) ◽  
pp. 35-39 ◽  
Author(s):  
Udai P. Singh ◽  
Sudha Singh ◽  
Sukh Mahendra Singh

Metal complexes of 5-carboxy-2-thiouracil with Mn(ll), Co(ll), Ni(ll), Cu(ll), Zn(ll) and Cd(ll) ions were synthesized, characterized, and subjected to a screening system for evaluation of antitumour activity against Sarcoma-180 (S-180) tumour cells. The complexes were characterized by elemental analysis, infrared, electronic spectra, room temperature magnetic measurements and powder X-ray diffraction. The antitumour activity results indicate that some complexes have antitumour activity both in vivo and in vitro against S-180 tumour cells.


2017 ◽  
Vol 72 (8) ◽  
pp. 579-584 ◽  
Author(s):  
Feng Da Bao ◽  
Ya Jie Ruan ◽  
Ge Ge Du ◽  
Shu Kai Zou ◽  
Jie Zhang ◽  
...  

AbstractTwo metal-organic coordination polymers constructed from tris(p-carboxylphenyl)phosphine oxide (TPOH3), namely, [Zn(TPOH)(2,2′-bipy)(H2O)·H2O·DMF]n (1) and [Zn2(TPOH)2(1,4-bix)2·5H2O]n (2) (2,2′-bipy=2,2′-bipydine, 1,4-bix=1,4-bis(imidazol-1-ylmethyl)benzene), were synthesized and identified by IR, elemental analysis and single-crystal X-ray diffraction analysis. Both of the 2,2′-bipy and 1,4-bix ligands tailor the complexes 1 and 2 into chain structures. The thermal behavior and solid state photoluminescence properties correlated with the corresponding structural features were investigated.


Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1329
Author(s):  
Agnieszka Ostasz ◽  
Alexander M. Kirillov

Two new 3D coordination polymers (CPs), formulated as [Zn(p-XBT)]n (1H) and [Cd(p-XBT)]n (2H), were assembled from a virtually unexplored p-xylylene-bis(2-mercaptoacetic) acid linker (p-XBTA) and characterized by infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), thermal analysis methods (TG-DSC, TG-FTIR), single-crystal X-ray diffraction, and topological analysis. Two different synthetic strategies were explored, namely the precipitation (P) and hydrothermal (H) methods, resulting in a Zn(II) derivative [Zn(p-XBT)·H2O]n (1P) and its dehydrated analogue [Zn(p-XBT)]n (1H), respectively. In the Cd(II)-containing system, the same [Cd(p-XBT)]n (2P = 2H) products were generated by both synthetic methods. Upon dehydration, 1P undergoes a “crystal-to-crystal” phase transition in the 170−185 °C temperature range, producing an anhydrous polycrystalline sample (1H). Both CPs 1H and 2H are isostructural and feature polymeric 3D metal-organic nets of the cds topological type, which are driven by the 4-linked metal and p-XBT2− nodes. These compounds represent unique examples of coordination polymers derived from p-xylylene-bis(2-mercaptoacetic) acid, thus opening up the use of this flexible S,O-heterodonor building block in the design of polymeric metal-organic architectures.


2019 ◽  
Vol 75 (6) ◽  
pp. 643-649 ◽  
Author(s):  
Xiao-Fei Li ◽  
Di Cheng ◽  
Xiang-Ru Meng ◽  
Huai-Xia Yang

Compared with the monomorphic type of ligand, combining mixed ligands in one coordination polymer offers greater tunability of the structural framework. Employment of N-heterocyclic ligands and aromatic polycarboxylates is an effective approach for the construction of metal–organic frameworks (MOFs). Two new coordination polymers incorporating both 2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole (imb) and benzenedicarboxylic acid isomers, namely, catena-poly[[[di-μ-chlorido-bis[(2-carboxybenzoato-κ2 O 1,O 1′)cadmium(II)]]-bis{μ-2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole-κ2 N:N′}] dihydrate], {[Cd(C8H5O4)Cl(C11H10N4)]·H2O} n , (I), and poly[[aqua(μ2-benzene-1,3-dicarboxylato-κ3 O 1,O 1′:O 3){μ2-2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole-κ2 N:N′}cadmium(II)] dihydrate], {[Cd(C8H4O4)(C11H10N4)(H2O)]·2H2O} n , (II), have been prepared and structurally characterized by single-crystal X-ray diffraction. In polymer (I), imb ligands bridge CdII ions, forming a one-dimensional chain, and 2-carboxybenzoate anions coordinate to the CdII ions in a terminal fashion. Polymer (II) exhibits a two-dimensional network structure in which imb ligands and the benzene-1,3-dicarboxylate anions join CdII ions co-operatively. This indicates that changing of the aromatic dicarboxylic acids can result in polymers with different compositions and architectures. Moreover, their IR spectra, PXRD (powder X-ray diffraction) patterns, thermogravimetric analyses and fluorescence properties were also investigated.


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