Xiu-Teng Wang

A {Co32} Nanosphere Supported by p-tert-Butylthiacalix[4]arene

Calixarene-capped Co(32) clusters are constructed by a sodalite Co(II)(24) cage and an encapsulated Co(III)(8) cube. The spherical units are arranged into three isomeric structures, two of which are stacked by the bcc lattices and the third of which is assembled by the cubic closest packing of the spherical units.

Two MnII2LnIII4 (Ln = Gd, Eu) hexanuclear compounds of p-tert-butylsulfinylcalix[4]arene

Two 3d-4f heterometallic compounds of p-tert-butylsulfinylcalix[4]arene were synthesized by the solvothermal method and characterized by some hinged double-dumbbell-like subunits in which two perpendicular dumbbell entities were constructed by an in-between isosceles triangle Mn(II)Ln(III)(2), and two tail-to-tail calixarene molecules, and hinged by the lanthanide-sulfinyl group bonding. The magnetic properties of the title compounds were examined.

Synthesis, structures, and magnetism of three 1D Mn(III) chains with oxazoline-based ligands.

Three novel Mn(III) polymers, [Mn(phox)(2)(N(3))](n) (1), [Mn(Etphox)(2)(N(3))](n) (2), and [Mn(Etphox)(2)(C(2)N(3))](n) (3), using achiral ligand Hphox (Hphox = 2-(4,5-dihydrooxazol-2-yl)phenol) and chiral ligand HEtphox (HEtphox = 2-(4-ethyl-4,5-dihydrooxazol-2-yl)phenol) were synthesized and structurally and magnetically characterized. All complexes are of 1D chain structures and form 2D frameworks by weak interactions. The adjacent 1D chains of complex 1 are connected by face-to-face pi-pi interactions, C-H...pi interactions, and hydrogen bonding, which leads to the formation of a supramolecular 2D sheet structure. The three compounds show antiferromagnetic coupling between Mn(III) ions. And compound 2 is a spin-canted weak ferromagnet with T(N) = 5.6 K, showing metamagnetic behavior with a two-step magnetic phase transition.

Two EE-azido-bridged nickel(II) layered compounds: vigorous twisted torsion angle Ni-N3-Ni results in ferromagnetic behavior.

Two coordination polymers, Ni(endi)(N(3))(2) (endi = 1,2-bis(tetrazol-1-yl)ethane) (1) and Ni(4-acpy)(2)(N(3))(2) (4-acpy = 4-acetylpyridine) (2), are obtained by employing a couple of cobalt complex as references. Both compounds have similar 2D (4,4) EE azide-nickel layer structures, but different interlayer separations. Their EE azide bridges are vigorously twisted, with the torsion angle tau value 88.3 degrees and 107.6 degrees for 1 and 89.2 degrees for 2. Different from most EE azide compounds, ferromagnetism is distinctly present, ordering below T(c) = 25 K for 1 and T(c) = 23 K for 2. Fitting of magnetic susceptibility data using the spin Hamiltonian H = -2J SigmaS(1)S(2) gives the ferromagnetic intralayer coupling J = 14.70(6) cm(-1) for 1 and 14.32(0) cm(-1) for 2, respectively. The magnetostructural correlations of 1 have been calculated using the density function theory based method. The computational results are consistent with the trend of the experimental data. One possible mechanism was proposed to explain the emergence of ferromagnetism based on the theoretical studies, and the ferromagnet construction approach was also proposed accordingly.