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Three MnII complexes, named Mn2(HATNA)2(CH3OH)4 (1), {[Mn3(ATNA)2(DMF)2(H2O)2]·0.5DMF·0.5H2O}n (2, DMF = N,N-dimethylformamide), and {[Mn6(ATNA)4(H2O)10]·8DMSO·2.5H2O}n (3, DMSO = dimethyl sulphoxide), were successfully synthesized by the reaction of the ligand azotetrazole-3-hydroxy-2-naphthoic acid (H3ATNA) and Mn(CH3COO)2 in CH3OH, DMF, and DMSO, respectively. A binuclear structure was found for complex 1, with the two Mn(II) ions doubly bridged through N–N linkers from the two tetrazole rings. Both 2 and 3 displayed one-dimensional structures. Magnetic studies show that antiferromagnetic interactions of Mn(II) ions existed in complexes 1–3. All the complexes exhibited luminescence emission peaks at room temperature. [ABSTRACT FROM AUTHOR]

A new compound of azotetrazole-3-hydroxy-2-naphthoic acid (H3ATNA) has been successfully synthesized and characterized. By controlling the ratio of metal ions to the ligand and the pH value of solution, mononuclear, dinuclear and tetranuclear dysprosium(III) complexes [Et3NH]3[Dy(HATNA)3]·5H2O (1), [Dy2(HATNA)3(DMF)(H2O)]·2DMF·CH3OH·2H2O (2) and [Et3NH]6[Dy4(ATNA)6(H2O)2]·DMF·2CH3CN·8H2O (3) were synthesized and characterized by X-ray diffraction crystallography (DMF = N,N-dimethylformamide). Crystallographic data demonstrate that the neutral H3ATNA exists as a hydrazone tautomer. Complex 1 is a mononuclear structure, in which the Dy(III) ion is a nine-coordinated ion surrounded by three tridentate HATNA− ligands. Complex 2 shows a dinuclear structure, which is bridged by three μ1,1-hydroxyl groups of three HATNA− ligands. In complex 2, the Dy(III)1 ion is a nine-coordinated ion surrounded by three tridentate HATNA− ligands, while Dy(III)2 is an eight coordinated atom with three tridentate HATNA− ligands, one DMF and one water molecule. Complex 3 displays a tetranuclear structure, which can be approximately considered as two μ1,3-carboxyl groups of ATNA3− ligands linking complex 2. The magnetic properties of 1–3 were investigated. Complexes 2 and 3 display slow magnetic relaxation in a zero dc field. [ABSTRACT FROM AUTHOR]

Through the self-assembly of a Salamo-type ligand H2L (H2L = 1,2-bis(3-methoxysalicylideneaminooxy)ethane) with Ni(OAc)2·4H2O, Ln(NO3)3·6H2O (Ln(iii) = La(iii), Gd(iii), Tb(iii) and Dy(iii)) and Py (Py = pyridine) or 4,4′-bipy (4,4′-bipy = 4,4′-bipyridine) or H2bdc (H2bdc = terephthalic acid), nine new Ni(ii)–Ln(iii) heterometallic complexes [Ni(L)La(OAc)(NO3)2(Py)(CH3OH)]·CH3OH (1), [Ni(L)Dy(OAc)(NO3)2(Py)] (2), 1∞[Ni(L)La(NO3)3(4,4′-bipy)(CH3OH)] (3), 1∞[Ni(L)Tb(NO3)3(4,4′-bipy)] (4), [Ni(L)Dy(OAc)(NO3)2(4,4′-bipy)] (5), [{Ni(L)Ln(NO3)2(DMF)(CH3OH)}2(bdc)] (Ln = La (6) and Gd (7)) and [{Ni(L)Ln(NO3)2(DMF)}2(bdc)] (Ln = Tb (8) and Dy (9)) were obtained, respectively. The acetato ligand bridges the Ni(ii) and Ln(iii) (Ln = La (1) and Dy (2)) atoms in a μ2 fashion and the Py coordinates to the apical position by a nitrogen atom in the heterobimetallic complexes 1 and 2. Complexes 3 and 4 are 1D coordination polymers constructed from heterobimetallic [Ni(L)Ln] (Ln = La (3) and Tb (4)) units which are connected by the exo-dentate ligand 4,4′-bipy bearing nitrogen-donor atoms, but complex 5 is a heterobimetallic Ni(ii)–Dy(iii) complex which is prepared under the same reaction conditions as complexes 3 and 4. Four heterotetranuclear dimers were constructed from heterobimetallic [Ni(L)Ln] (Ln = La (6), Gd (7)), Tb (8) and Dy (9) units which are connected by the exo-dentate H2bdc ligand with oxygen-donor atoms. Magnetic measurements were performed on the Gd(iii), Tb(iii) and Dy(iii) complexes. [ABSTRACT FROM AUTHOR]

Two new MnII supramolecular isomers, [Mn2(pbt)2(H2O)2·2H2O]n (1) and [Mn2(pbt)2(H2O)2·DMF]n (2) (H2pbt = 5′-(pyridin-2-yl)-2H,4′H-3,3′-bi(1,2,4-triazole), DMF = N,N-dimethylformamide), have been solvothermally synthesized in different solvent systems. Compound 1 exhibits a (3,4)-connected net with the point symbol of (6.82)4(62.82.102), whereas 2 exhibits a rare 3D lvt-42·84 net. Moreover, an irreversible solid-state transformation from 2 to 1 was observed, and their magnetic properties were also investigated and discussed in detail. [ABSTRACT FROM AUTHOR]