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Two novel Co (II)‐ coordination polymers (CPs) based on 2,5‐bis(4‐carboxylpheny)‐1,3,4‐oxadiazole (bcpo), namely [Co/(bcpo)0.5(tib)(H2O)2]n (1) and [Co (bcpo)0.5(bidpe)(H2O)2]n (2) (tib = 1,3,5‐tirs(1‐imidazolyl)benzene, bidpe = 4,4′‐bis (imidazolyl)diphenyl ether) have been synthesized under solvothermal conditions and characterized by powder X‐ray diffraction (PXRD), single crystal X‐ray diffraction, photochemistry as well as electrochemistry. The investigation of the photo‐degradation methyl blue and methyl violet (MB, MV) properties of CPs 1–2 demonstrates that CP 1 shows great performance for the degradation of MB, and CP 2 could efficiently degrade MB/MV. Meanwhile, the possible photo‐degradation mechanism has been proposed and explored. Simultaneously, electrochemistry studies show that both CPs 1 and 2 can catalyze water oxidation under an alkaline condition at the potential around 1.20 V vs. NHE with relatively low overpotential of 330–510 mV vs. NHE. [ABSTRACT FROM AUTHOR]

A novel metal organic framework, namely, {[Zn3(btc)2(bimmb)2.5]·2H2O·CH3CN}n (1) (btc = 1,3,5-benzenetricarboxylic acid), bimmb = 1,4-bis(imidazol-l-ylmethyl) benzene), has been reasonably designed, successfully solvothermally synthesized, and characterized. The complex is characterized by elemental analysis, IR spectroscopy, single-crystal X-ray diffraction, thermogravimetric analysis, and powder X-ray diffraction. Complex 1 exhibits a 5-nodal 3,3,4,4,6-connected 3D framework with a (5·6·7)2(52·8)2(52·92·102)2(53·82·9)2(54·62·72·84·92·11) topology. The photodegradation studies reveal that complex 1 displays highly sensitive photodegradation sensing toward methylene blue, rhodamine B, and methyl violet under UV irradiation. [ABSTRACT FROM AUTHOR]

Two novel Co(II) coordination polymers (CPs), formulated as {[Co 2 (L)(H 2 O) 6 ]·H 2 O} n (1) and {[Co(bidpe) 2 (H 2 O) 2 ]·H 2 L·3.5H 2 O} n (2) (H 4 L = 3,5-bis(3,4-dicarboxylphenoxy)pyridine, bidpe = 4,4′-bis(lmidazolyl)diphenyl ether), have been solvothermally synthesized and characterized by various techniques. Complex 1 exhibited a 2D→3D supramolecular framework through H-bonds with a point symbol of (12)(4·125)(4) topology. However, with the introduction of additional bibpe ligand, the H 4 L ligand did not coordinate with Co(II) ions in the synthesis of 2. Complex 2 possessed a 1D [Co(bidpe) 2 ] n loop line, which was further linked by H-bonds to form a 3D supramolecular architecture. In particular, both the CPs exhibited efficient photocatalytic activities towards the degradation of methyl violet (MV) under low-energy irradiation of a 125 W Hg lamp, which could be attributed to their high efficiencies in generating ·OH radicals. Moreover, the variable-temperature magnetic analyses indicated that 1 and 2 exhibit antiferromagnetic behavior between the adjacent Co(II) ions. Two novel Co(II)-CPs are applied to the UV-light-driven degradation of methyl violet (MV) with small dosage and low-energy irradiation. [Display omitted] • Two novel Co(II)-CPs under solvothermal condition in one-step, for the first time, were synthesized. • The obtained Co(II)-CPs can act as efficient and recyclable photocatalysts for the UV-light-driven degradation of methyl violet with small dosage and low-energy irradiation. • The obtained Co(II)-CPs exhibit antiferromagnetic coupling between adjacent central Co(II) ions. [ABSTRACT FROM AUTHOR]

Two novel Ni(II)-based monomeric complexes are applied to the UV-light-driven degradation of methyl violet (MV). [Display omitted] Two Ni(II)-based monomeric complexes with the formulas of [Ni(dbb)(H 2 O) 2 ] (1) and [Ni 2 (H 2 dbb) 2 (xda)(H 2 O) 2 ] (2) (H 2 dbb = 6,6′-di(benzimidazol-2-yl)-2,2′-bipyridine, H 4 xda = 5,5′-(1,4-xylylenediamino) diisophthalic acid) have been successfully synthesized under solvothermal conditions. Structural analysis revealed that the discrete monomers of 1 and 2 extend into high-dimensional networks through intermolecular hydrogen bonds, π···π stacking interactions and weak intermolecular interactions. As novel photocatalyst materials, 1 and 2 exhibited active performance towards the degradation of methyl violet (MV) under UV irradiation. Besides, the cyclic experiments indicated that 2 was stable and reusable, enabling it to be potential candidates for dye-containing wastewater treatment. The possible mechanism of the photocatalytic performance was also investigated in detail. Moreover, the magnetic susceptibility measurements of 1 and 2 demonstrated that week antiferromagnetic interactions were operative between the Ni(II) ions. [ABSTRACT FROM AUTHOR]

Three novel Mn(II)/Co(II)-based 3D metal-organic frameworks (MOFs), namely {[Mn 2 (L)(tib)(H 2 O)]·3DMA·4H 2 O} n (1), {[Co 2 (L)(bipd) 2 ]·3H 2 O} n (2) and {[Co(L) 0.5 (bimb)]·3H 2 O·0.5O 2 } n (3) (H 4 L ​= ​5,5'-(1,4-xylylenediamino) diisophthalic acid, tib ​= ​1,3,5-tris(1-imidazolyl)benzene, bipd ​= ​3,5-bis(1-imidazoly)pyridine, and bimb ​= ​1,4-bis(lmidazol)-butane), have been successfully synthesized using the mixed-ligand as functionalized organic linker. The structural characterization revealed that both MOFs 1 and 2 exhibited an unprecedented 4-nodal 3D framework that enriching crystal engineering, while MOF 3 featured a 2-nodal three-interpenetrating bbf topology framework with a Schläfli symbol of (64·82)(66) 2. The title MOFs have been exploited as photocatalysts for degradation of methylene blue (MB), methyl violet (MV) and malachite green (MG). The photocatalytic results demonstrated that MOFs 2 and 3 exhibited efficient photocatalytic abilities to degrade the three aromatic dyes under UV irradiation. The possible catalytic mechanism was also explored and discussed in detail. Moreover, the variable-temperature magnetic analyses indicated that MOFs 1 – 3 exhibited weak antiferromagnetic behavior between Mn(II)/Co(II) ions. [Display omitted] • Three novel Mn(II)/Co(II)-based 3D MOFs under solvothermal or hydrothermal condition in one-step, for the first time, were synthesized. • The MOFs 2 and 3 act as efficient heterogeneous photocatalyst for degradation of three aromatic dyes. • The possible catalytic mechanism was explored and discussed in detail. • MOFs 1 – 3 exhibit antiferromagnetic coupling between neighboring central ions. [ABSTRACT FROM AUTHOR]