Five Mn(II) Coordination Polymers Based on 2,3′,5,5′-Biphenyl Tetracarboxylic Acid: Syntheses, Structures, and Magnetic Properties was written by Zhao, Ying;Chang, Xin-Hong;Liu, Guang-Zhen;Ma, Lu-Fang;Wang, Li-Ya. And the article was included in Crystal Growth & Design in 2015.Category: imidazoles-derivatives The following contents are mentioned in the article:
Five manganese(II) coordination polymers with 2,3′,5,5′-biphenyl tetracarboxylic acid (H4bptc) and five N-donor ancillary ligands, {[Mn2(bptc)(2,2′-bipy)2]·2H2O}n (1), {[Mn2(H2bptc)2(phen)4]·6H2O} (2), {[Mn3(Hbptc)2(4,4′-bipy)4(H2O)4]·4H2O}n (3), {[Mn2(bptc)(1,4-biyb)2]}n (4), and {[Mn3(Hbptc)2(biip)2(H2O)2]}n (5) [2,2′-bipy = 2,2′-bipyridine, phen = 1,10-phenanthroline, 4,4′-bipy = 4,4′-bipyridine, 1,4-biyb = 1,4-bis(imidazol-1-ylmethyl)benzene, biip = 3,5-bis(1-imidazol)pyridine], were synthesized under hydrothermal conditions. Complexes 1–5 were structurally characterized by elemental anal., IR spectra, x-ray single-crystal diffraction, and powder X-ray diffraction (PXRD). Complex 1 exhibits a 2D layered structure with a (3,6)-connected (43)2(46.66.83) topol. Complex 2 shows a 0D structure and further stacks via hydrogen-bonding interactions to give a 3D supramol. architecture. Complex 3 possesses a 3D structure with a 4-connected (4.63.82)(44.62)(43.63) topol. Complex 4 displays a 3D structure with a (4,5)-connected (4.52.6.7.8)(5.64.74.8)(4.52.62.74.8) topol. Complex 5 features a 3D structure with a (4,5,6)-connected (42.64)(43.67)(42.68.73.82) topol. Magnetic susceptibility measurements indicate weak antiferromagnetic interactions between the Mn(II) ions in 1, 2, and 4. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Category: imidazoles-derivatives).
3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Category: imidazoles-derivatives
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem