Publications by authors named "Yan-Feng Yue"

Enterospora epinepheli is an intranuclear microsporidian parasite causing serious emaciative disease in hatchery-bred juvenile groupers (Epinephelus spp.). Rapid and sensitive detection is urgently needed as its chronic infection tends to cause emaciation as well as white faeces syndrome and results in fry mortality.

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Unlabelled: The synthesis, bioassays and nano-structure characterization of Cu(II)-RGD-octapeptide complexes Cu(II)-Arg-Gly-Asp-Ser-Arg-Gly-Asp-Ser [Cu(II)-4a], Cu(II)-Arg-Gly-Asp-Val-Arg-Gly-Asp-Val [Cu(II)-4b] and Cu(II)-Arg-Gly-Asp-Phe-Arg-Gly-Asp-Phe [Cu(II)-4c] were investigated. UV-vis, CD and CD/ESI-MS spectra suggested that the coordination of Cu(II)-4a-c met a 3 N mode. In the in vitro anti-platelet aggregation assay the IC(50) values of Cu(II)-RGD-octapeptide complexes were 10 - 110 folds lower than that of RGD-octapeptides.

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Two 2D Mn (II) complexes, [Mn3(TzDC)2(phen)3] x 2 H2O (1; H3TzDC = 1,2,3-triazole-4,5-dicarboxylic acid, phen = 1,10-phenanthroline) and [Mn3(TzDC)2(bipy)3] x 4 H2O (2; bipy = 2,2'-bipyridine), were synthesized by hydrothermal reactions and characterized magnetically, and complex 1 was the first example of the chiral complex with a Kagomé lattice connectivity obtained through spontaneous resolution.

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A 3D heterometallic compound, [Cu4Na4(TzDC)4(H2O)7]n (H3TzDC = 1,2,3-triazole-4,5-dicarboxylic acid), which contains unprecedented planar "Na within [Cu4]" metalloporphyrin-like subunits, was synthesized by hydrothermal reactions involving in situ formation of the ligand and templated assembly of the metalloporphyrin-like subunits.

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One-dimensional zigzag coordination chains in four different directions are hierarchically entangled to generate an unprecedented 3D interwoven framework, which exhibits permanent porosity and guest selectivity.

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Using the achiral diazine ligands bearing two bidentate pyridylimino groups as sources of conformational chirality, five azido-bridged coordination polymers are prepared and characterized crystallographically and magnetically. The chirality of the molecular units is induced by the coordination of the diazine ligands in a twisted chiral conformation. The use of L(1) (1,4-bis(2-pyridyl)-1-amino-2,3-diaza-1,3-butadiene) and L(2) (1,4-bis(2-pyridyl)-1,4-diamino-2,3-diaza-1,3-butadiene) induces spontaneous resolution, yielding conglomerates of chiral compounds [Mn(3)(L(1))(2)(N(3))(6)](n) (1) and [Mn(2)(L(2))(2)(N(3))(3)](n)(ClO(4))(n).

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Three one-dimensional (1D) azido-bridged coordination polymers of formula [Cu(L)(N3)2]n (1), [Cu2(Me-L)(N3)4]n (2), and [Mn(L)(N3)2]n (3) have been synthesized and structurally characterized, and their magnetic properties studied, where L and Me-L are 2-(pyrazol-1-ylmethyl)pyridine and 2-(3-methylpyrazol-1-ylmethyl)pyridine, respectively. Compound 1 consists of 1D chains in which the Cu(II) ions with a square pyramidal geometry are alternately bridged by an end-to-end (EE) and an end-on (EO) azido ligands, both adopting a basal-apical disposition. Compound 2 exhibits an unprecedented chain topology built via three different kinds of EO azido bridges.

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Five Mn(II)[bond]azido coordination polymers of formula [Mn(L)(N(3))(2)](n) have been synthesized and crystallographically characterized, and their magnetic properties studied, where L's are the bidentate Schiff bases obtained from the condensation of pyridine-2-carbaldehyde with aniline (1) and its derivatives p-toluidine (2), m-toluidine (3), p-chloroaniline (4), and m-chloroaniline (5). All the complexes consist of the zigzag Mn(II)[bond]azido chains in which the Mn(II) ions are alternately bridged by two end-to-end (EE) and two end-on (EO) azido ligands, the cis-octahedral coordination being completed by the two nitrogen atoms of the Schiff base ligands. Compound 2 is unique in that the Mn[bond](EE-N(3))(2)[bond]Mn ring adopts an unusual twist conformation with the two linear azido bridges crossing each other.

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