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梁宏, LIANG, Hong*, CHEN, Xiong-Bin, Zhen-Feng, HU, Rui-Xiang, YU, Kai-Bei
CHINESE JOURNAL.OF CHEMISTRY 2002, 20, 650-656,-0001,():
-1年11月30日
The reaction of picolinic acid (Hpic) and (n-Bu4N)4[MosO26] in the presence of CH3CN gave a supramolecular compound (n-Bu4N)2[Mo2O6(pic)2] (1), and its structure was characterized by elemental analysis, IR spectra and single crystal Xray diffraction analysis. The single crystal X-ray diffraction study shows that the crystal is in monocnnic crystal system, P21/c space group with cell parameters a=0.9941 (2), b=1.3719(2), c=1.8824(2)nm, β=100.840(10)°, Mr=508.50, V=2.5214(9)nm3, F(000)=1072. Compound 1 is a dimer through two μ2-O bridging to two MoO3 (pic)-unit, then connected one-dlmensional anion-chain by undassical hy-drogen bonding, and the anion-chain across the channels formed via (n-Bu4N)+ cations. By means of undassical hydrogen bonding, the anion-chain and cationchannels assemble into three-dimensional supramolecular networks.
molybdenum (, Ⅵ), complex,, crystal structure,, hydrogen bonding,, supramolecular networks
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梁宏, Hong Liang*, Qing Yu and Rui-Xiang Hu, Zhong-Yuan Zhou and Xiang-Ge Zhou
,-0001,():
-1年11月30日
The Schiff-base (PNOAAP) derived from picolinaldehyde N-oxide and 4-aminoantipyrine, and its copper(Ⅱ) complex: [Cu(PNOAAP)2(EtOH)2]2(ClO4)4 (1) has been prepared and characterized by elemental analysis, i.r., 1H n.m.r, spectrum, and single crystal X-ray crystallographic determination. The PNOAAP ligand isomerizes from trans to cis after chelating to copper(Ⅱ).
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【期刊论文】Studies on the interaction between Ag and human serum albumin
梁宏, Xing-Can Shen a, b, Hong Liang b, Jun-Huai Guo a, Cheng Song b, Xi-Wen Hea a, *, Yu-Zhou Yuan b
Journal of Inorganic Biochemistry 95 (2003) 124-130,-0001,():
-1年11月30日
The interaction between Ag+ and human serum albumin (HSA) has been intensively studied by means of equilibrium dialysis, ligand-to-metal charge transition (LMCT) bands, circular dichroism (CD) and Raman spectroscopy. Scatchard analysis of the results of 1 equilibrium dialysis indicates the presence of two types of binding sites for Ag+ on HSA, and the orders of magnitude of binding stability 54 constants are found to be 10 5 and 10 4, respectively. During the binding process, a gradual increase in absorbance values of LMCT bands is observed with time-scanning UV absorption spectra, implying the Ag(Ⅰ) centers are continually formed in HSA. The time-scanning CD1 spectra provide evidence that the binding of Ag+ induces HSA to undergo a slow rearrangement of tertiary structure, and to change from 11 the original conformation in the absence of Ag (B-state) to conformation binding with Ag (A-state). The rate constants and activation free energy of A-B transition are calculated. The Raman spectrum of Ag(Ⅰ)-HSA system shows distinct vibration bands at 224 and 246 21cm in the low-frequency region, which significantly reveal the formation of Ag-S and Ag-N bonds. In addition, the electrostatic 1 interaction between Ag+ and negatively charged oxygen is also detected with Raman spectroscopy.
Ag(, Ⅰ), -serum albumin, Equilibrium constant, Conformation transition, Activation free energy, Coordination analysis
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【期刊论文】Binding equilibrium of I
梁宏, LIANG Hong, SHEN Xingcan, JIANG Zhiliang, HE Xiwen & SHEN Panwen
SCIENCE IN CHINA (Series B) December 2000 Vol. 43 No.6 600~608,-0001,():
-1年11月30日
The binding equilibrium between I- and human serum albumin (HSA) or bovine serum albumin (BSA) has been studied by means of the resonance Rayleigh scattering (RRS) and equi librium dialysis. It has been found for the first time that RRS and multiple frequency scattering (MFS) are enhanced as the I- binding to the HSA and BSA, but fluorescence quenches. The equilibrium dialysis results suggest that the binding of I
serum albumin,, iodine ion,, resonance Rayleigh scattering,, equilibrium dialysis,, phase distribution.,
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梁宏, Xing-Can Shen, Xiu-Zhong Fang, Ying-Hua Zhou, and Hong Liang
Chemistry Letters Vol. 33, No.11 (2004) 1468~1469,-0001,():
-1年11月30日
The aminosilane-modified magnetite nanoparticles were synthesized by the coprecipitation and surface modification with 3-aminopropyltriethoxysilane (APTTS). The superparamagnetic APTTS/Fe3O4 nanospheres with an average diameter of 10nm were characterized significantly with functional group, well dispersion and stabilization in aqueous fluids, as well as a maximized saturation magnetization of 63.54emu/g.
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