Publications by authors named "Ai-Ju Zhou"

A facile and efficient cyclization of sodium aminodiboranate to construct a boron-nitrogen-hydrogen ring is presented. This new strategy can be developed into a general method to prepare aminodiborane and its derivatives. Theoretical calculations show that a one-step cyclization mechanism is favored, where the dihydrogen bond plays an important role.

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Two isostructural mononuclear Co complexes, [Co(xantpo)(NCE) ] (E=S (1) and O (2); xantpo=9,9-dimethyl-4,5-bis(diphenylphosphoryl) xanthene), supported by a bidentate phosphine oxide ligand are reported. The cobalt complexes exhibit characteristic tetrahedral structures coordinated with two oxygen and two nitrogen atoms. Magnetic property measurements show their similar static magnetic behaviours but very different dynamic magnetic behaviours.

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Carbon material containing nickel, nitrogen and sulfur (Ni-NSC) has been synthesized using metal-organic frameworks (MOFs) as precursor by annealing treatment with a size from 200 to 300 nm. Pd nanoparticles supported on the Ni-NSC (Pd/Ni-NSC) are used as electrocatalysts for ethanol oxidation in alkaline media. Due to the synergistic effect between Pd and Ni, S, N, free OH radicals can form on the surface of Ni, N and S atoms at lower potentials, which react with CHCO intermediate species on the Pd surface to produce CHCOO and release the active sites.

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Eight isostructural lanthanide coordination polymers [Ln(bptc)(phen)(H2O)]n (Ln = Dy for , Eu for , Tb for , Gd for , Sm for , Nd for , Yb for , Pr for ) were successfully prepared based on bridging asymmetric polycarboxylate ligand biphenyl-3,2',5'-tricarboxylic acid (H3bptc) and chelating 1,10-phenanthroline (phen) coligand. Single crystal X-ray analysis reveals that complexes have a (3,6)-connected CdI2-type coordination network consisting of paddle-wheel dimers [Ln2(CO2)4]. The magnetic and fluorescent properties of have been investigated.

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The use of flexible N,N,N',N'-tetrakis(2-hydroxyethyl)ethylenediamine has provided one new high symmetry superoctahedron with unprecedented aesthetically-pleasing Mn(III)18 clusters, which exhibits out-of-phase signals indicative of the slow magnetic relaxation.

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Reactions of N,N,N',N'-tetrakis(2-hydroxyethyl)ethylenediamine (H(4)edte) with MnCl(2).4H(2)O or FeCl(3).6H(2)O in MeOH or MeCN with different bases yield four butterfly-like tetranuclear clusters with fused defective dicubane M(4)O(6) cores: [Mn(II)(2)Mn(IV)(2)(mu(4)-Hedte)(2)(thme)(2)].

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Room-temperature reactions of N,N,N',N'-tetrakis(2-hydroxyethyl)ethylenediamine with manganese(II) salts yield a novel family of Mn(12) clusters incorporating the same Mn(12)O(4) core and tunable oxidation states of Mn(III)(x)Mn(II)(12-x) (x = 8, 10, and 12). Magnetic susceptibility data indicate that the spin of the ground state increases as the number of Mn(III) ions is increased, leading to increases in the magnitude of the out-of-phase ac susceptibility signal as the number of Mn(III) ions is increased.

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