Cytochalasans from the Endophytic Fungus sp. LE2: Their Structures, Antibacterial and NO Production Inhibitory Activities.

Six new cytochalasans-namely, aspergicytochalasins A-F (-)-together with five known analogs were isolated and characterized from the endophytic fungus sp. from the medicinal plant . The structures of the new compounds were established by NMR and MS methods as well as single crystal X-ray diffractions.

Tuning Slow Magnetic Relaxation in a Two-Dimensional Dysprosium Layer Compound through Guest Molecules.

A novel two-dimensional dysprosium(III) complex, [Dy(L)(CH3COO)]·0.5DMF·H2O·2CH3OH (1), has been successfully synthesized from a new pyridine-N-oxide (PNO)-containing ligand, namely, N'-(2-hydroxy-3-methoxybenzylidene)pyridine-N-oxidecarbohydrazide (H2L). Single-crystal X-ray diffraction studies reveal that complex 1 is composed of a dinuclear dysprosium subunit, which is further extended by the PNO part of the ligand to form a two-dimensional layer.

Thermostability and photoluminescence of Dy(iii) single-molecule magnets under a magnetic field.

A series of compounds [ADyL]·[solvent] composed of a dysprosium(iii) ion coordinated by four chelated naphthyridine-like ligands (L = 4-hydroxy-8-methyl-1,5-naphthyridine-3-carbonitrile) and an alkali metal ion (A = Na, K, Rb, Cs) were synthesized and characterized. They behave as single-molecule magnets under a zero dc field with an effective energy barrier of around 95 cm. Meanwhile, the main part, [ADyL], of these SMMs is thermostable and sublimable.

Facile synthesis of magnetic homochiral metal-organic frameworks for "enantioselective fishing".

Magnetic functionalized homochiral metal-organic frameworks (MOFs) were prepared and applied to efficient enantioselective fishing of chiral drug intermediates. Under optimized conditions, the enantiomeric excess (ee) value as high as 85.2% was achieved for methyl phenyl sulfoxide (MPS) within 3 min.

A robust microfluidic device for the synthesis and crystal growth of organometallic polymers with highly organized structures.

A simple and robust microfluidic device was developed to synthesize organometallic polymers with highly organized structures. The device is compatible with organic solvents. Reactants are loaded into pairs of reservoirs connected by a 15 cm long microchannel prefilled with solvents, thus allowing long-term counter diffusion for self-assembly of organometallic polymers.

Metal-organic frameworks built from achiral 3-(5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl)benzoic acid: syntheses and structures of metal(II) complexes.

Using a novel flexible achiral ligand, 3-(5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl)benzoic acid (HL), four metal(II)-complexes formulated as ZnL2·2H2O (1), CdL2(H2O)2·8H2O (2) and ML2(H2O)·H2O (M = Co 3 and Ni 4) have been hydrothermally synthesized and structurally characterized by single-crystal X-ray diffraction. Complexes 1, 3 and 4 all feature a uninodal 2D layer with a 4(4)-sql topology, and two such (4,4) nets interpenetrate in a parallel manner. Complex 2 exhibits a similar 4(4)-sql topology, but no interpenetration is observed in complex 2.

Metal(II) complexes based on 1,4-bis(3-pyridylaminomethyl)benzene: structures, photoluminescence and photocatalytic properties.

Using a novel ditopic N-donor ligand, 1,4-bis(3-pyridylaminomethyl)benzene (L), four metal(II)-complexes formulated as CdL(SO4)(H2O)2 (1), CdL(1,3-bdc) (1,3-H2bdc = 1,3-benzene dicarboxylic acid) (2), PbL(1,3-bdc) (3) and ZnL(1/2)(2,5-tdc) (2,5-H2tdc = 2,5-thiophene dicarboxylic acid) (4) have been hydrothermally synthesized and structurally characterized by single-crystal X-ray diffraction. Complexes 1 and 3 feature uninodal 4-connected non-interpenetrated sql/Shubnikov tetragonal plane nets with {4(4).6(2)} topology.

Two novel Co(II) coordination polymers based on 1,4-bis(3-pyridylaminomethyl)benzene as electrocatalysts for oxygen evolution from water.

Based on the L (1,4-bis(3-pyridylaminomethyl)benzene) ligand, two MOFs formulated as Co(L)0.5(adip) (H2adip = adipic acid) (1) and Co2(L)2(5-bdc)2(H2O)2·H2O (2) (5-H2bdc = 5-nitroisophthalic acid) (2) were synthesized and structurally characterized by single-crystal X-ray diffraction. Complex 1 features a uninodal 4-connected non-interpenetrated sql/Shubnikov tetragonal plane net with {4(4).

Structural investigation of a fucoidan containing a fucose-free core from the brown seaweed, Hizikia fusiforme.

A fucoidan, obtained from the hot-water extract of the brown seaweed, Hizikia fusiforme, was separated into five fractions by DEAE Sepharose CL-6B and Sepharose CL-6B column chromatography. All five fractions contained predominantly fucose, mannose and galactose and also contained sulfate groups and uronic acid. The fucoidans had MWs from 25 to 950 kDa.