The mononuclear Zn(Ⅱ) complex [Zn(2,6-PDA)(phen)H2O]·H2O (1) and binuclear Cu(Ⅰ) complex{[Cu(μ-Ⅰ)(phen)H2O]·H2O}2 (2) (2,6-H2PDA=2,6- pyridinedicarboxylic acid,phen=1,10- phenanthroline monohydrate) have been prepared with hydro-thermal synthesis method. These complexes have been characterized with single-crystal X-ray, elemental analysis, and IR spectroscopy. The fluorescence spectra of 1 and 2 are studied in solid-state and dimethyl sulfoxide (DMSO) solution.
View Article and Find Full Text PDFThis work reports on two new complexes with the general formula [Cd3(IBA)3(Cl)2(HCOO)(H2O)]n (1) and {[Cd1.5(IBA)3(H2O)6]·3.5H2O}n (2), which can be synthesized by the reaction of Cd(II) with rigid linear ligand 4-HIBA containing imidazolyl and carboxylate functional groups [4-HIBA = 4-(1H-imidazol-1-yl)benzoic acid].
View Article and Find Full Text PDFGuang Pu Xue Yu Guang Pu Fen Xi
January 2015
A supramolecular Cd(II) complex[Cd(bpdc) (phen)2 (H2O)] . 6H20 (1) was synthesized with 2, 4'-biphenyldicarboxylic acid (H2bpdc) and 1, 10-phenanthroline (phen) under hydrothermal conditions and characterized by single-crystal X-ray diffraction elemental analysis, and IR spectrum. Single-crystal X-ray analysis reveals complex 1 crystalizes in the triclinic P 1 space group, the metal center Cd(II) ion is six-coordinated and exhibits a distorted octahedron geometry arrangement.
View Article and Find Full Text PDFA novel polydentate Schiff base ligand N(1),N(3)-bis[(6-methoxypyridin-2-yl)methylene]benzene-1,3-diamine (L) and its two dinuclear sandwich-like complexes {[CdL(NO3)(H2O)]·NO3}2 (1) and {[CdL(CH3CN)(H2O)]·(ClO4)2·(CH3CN)2}2 (2) were synthesized. Both C-H∙∙∙O, C-H∙∙∙N and π-π non-covalent interactions had essential roles in constructing the resulting three-dimensional supramolecular networks. L emits a more intense blue-green fluorescence emission around 493 nm than in dilute solution, exhibiting stacking-induced emission properties.
View Article and Find Full Text PDFA rare 3D tetranuclear {In4(μ2-OH)3} building block based MOF {[In4/3(μ2-OH)(2,6-pydc)(1,4-bda)0.5(H2O)]·2H2O}n (2) was obtained through a crystal transformation from a dimeric complex In3(2,6-pydc)3(1,4-bda)1.5(H2O)6 (1).
View Article and Find Full Text PDFTwo rare 2D Ga/In-based coordination polymers in which one metal center coexists with three distinct aromatic ligands were synthesized. Helical channels along the 21 screw axis are exhibited to form a hcb net. The compounds exhibit tunable fluorescence from blue, green, white to yellow light by varying the temperature and solvents.
View Article and Find Full Text PDFHepatitis B virus(HBV) infection remains a global problem, despite the effectiveness of the Hepatitis B vaccine in preventing infection. The resolution of Hepatitis B virus infection has been believed to be attributable to virus-specific immunity. In vivo direct evaluation of anti-HBV immunity in the liver is currently not possible.
View Article and Find Full Text PDFBackground/aims: Interferon beta (IFN-β) is the priming cytokine in the interferons (IFNs) response that plays essential roles in innate immune system. Only very few studies on IFN activation in animals have been reported before, therefore, we embarked to develop a novel method to dynamically examine IFN-β activation in mouse liver by noninvasive molecular imaging.
Methods: Interferon beta promoter-directed firefly luciferase gene was integrated into chromosomes of hepatocytes by hydrodynamic injection.
Background: The development of small molecule inhibitors of hepatitis C virus (HCV) core protein as antiviral agents has been intensively pursued as a viable strategy to eradicate HCV infection. However, lack of a robust and convenient small animal model has hampered the assessment of in vivo efficacy of any antiviral compound.
Methodology/principal Findings: The objective of this work was to develop a novel method to screen anti-core protein siRNA in the mouse liver by bioluminescence imaging.
To find new liver-specific expression cassettes for long-term expression of therapeutic genes in the context of pDNA, the function and specificity of hepatitis B virus (HBV)' two hepatic enhancers (EnI and EnII), combined with HBV core and X promoters in cultured cells were evaluated. By bioluminescence imaging and hydrodynamic gene transfer technology, the persistence of transgene expression containing these regulatory sequences in the liver of mice was assessed. Our data indicated that both HBV enhancers were able to stimulate HBV core and X promoter activity in cultured cells of hepatic origin.
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