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41.
脑神经退行性疾病中的有机化学-朊病毒(疯牛病)中的蛋白物理有机化学和自由基化学 总被引:5,自引:0,他引:5
杨池明 《高等学校化学学报》2002,23(2):243-250
通过关于“普里昂”蛋白病毒疾病的已有临床、医学生理、免疫和化学等方面的现象,讨论了朊病毒当中的部分蛋白氧化损伤和蛋白自由基化学本质。 相似文献
42.
Joël J. E. Moreau Luc Vellutini Catherine Bied Michel Wong Chi Man 《Journal of Sol-Gel Science and Technology》2004,32(1-3):63-67
The acid-hydrolysis of an organo-bridged bisdiethoxysilylated molecular precursor bearing urea groups, (EtO)2MeSi(CH2)3NHCONH(CH2)12NHCONH(CH2)3SiMe(OEt)2, has been performed in pure aqueous medium. Scanning electron microscopy (SEM) analysis of the resulting insoluble solid revealed plate-like forms with a lamellar structure as determined by powder X-ray diffraction (PXRD) studies with a sharp peak at 28.5 Å. The solid state 29Si MAS-NMR spectrum of this bridged siloxane hybrid is consistent with a moderately condensed material with complete preservation of the Si–C bonds throughout the hybrid network. In comparison, the classical sol–gel hydrolysis-condensation of the molecular precursor in ethanol with stoichiometric amount of water and fluoride anion as catalyst produced an amorphous featureless solid. 相似文献
43.
Blends of ABS (acrylonitrile–butadiene–styrene) with phenoxy(poly(hydroxyether bisphenol A)) were prepared using a Branender single screw extruder. Scanning and transmission electron micrographs (SEM, TEM) showed a typical two-phase morphology; particle-in-matrix (90/10) (ABS/phenoxy by weight), 70/30, 10/90), island/sea (30/70) and co-continuous (50/50) morphologies. The glass transition temperature (Tg) of SAN was almost unchanged in the blends, while the Tg of phenoxy increased by about 5 °C in the blends. The synergistic effect of tensile modulus and strength was noted in ABS-rich blends, where a drastic drop of ductility was seen, and the results were interpreted in terms of rubber particle migration form SAN to phenoxy phase, which was visualized by TEM. Melt viscosity showed yield in ABS-rich blends, and generally followed the log additivity. 相似文献
44.
45.
Chi -ping Lau 《manuscripta mathematica》1987,59(1):53-62
It is shown that if the order of non-uniformity of a quasi-linear elliptic equation is h,1
0,2(h–1)/h norm. For 0h1,existence of a bounded solution is guaranteed without any smallness assumption on the given boundary data.More precise information is given for the special case of the minimal surface equation. 相似文献
46.
Treatment of (thd)H (thd=2,2,6,6-tetramethyl-3,5-heptandionate) with excess Os3(CO)12 in an autoclave at 180°C gives the formation of a brown metal chain complex [Os2(CO)5(thd)2]2 (1) and a yellow CO2 cluster complex [Os4(-H)(-CO2)(thd)(CO)13] (2) in low yields. Complex 2 was fully identified by a combination of spectroscopic methods and X-ray diffraction study, showing a unique CO2 ligand bridging a triosmium metal fragment, Os3(-H)(CO)10 and a monometallic osmium fragment, Os(CO)3(thd). Upon treatment of 1 with Me3NO at an elevated temperature, oxidation of the CO ligand occurred at the position trans to the unique CO2 ligand on the Os(CO)3(thd) fragment, giving the formation of a second CO2 cluster [Os4(-H)(-CO2)(thd)(CO)12(NCMe)] (3), which is stabilized by a weakly coordinated acetonitrile molecule. 相似文献
47.
The keto-enol tautomerization of p-hydroxyphenylpyruvic acid (pHPP) in aqueous solutions and the complexation reaction between enolic pHPP and boric acid have been studied by electrochemical techniques including linear sweep voltammetry (LSV), pulse voltammetry, and cyclic voltammetry (CV), combining with UV spectrometry. Electrochemical techniques reveal that in aqueous solution, there are two tautomers of pHPP: enolic form and ketonic form; the former exists mainly in freshly prepared pHPP solution, and the latter exists mainly in equilibrium solution. Both enolic and ketonic pHPP are electroactive. The electrochemical oxidation of enolic pHPP gives rise to two anodic waves, I(a) and II(a), while the electrochemical oxidation of ketonic pHPP only results in the observation of the second wave II(a). The oxidation process I(a) is revealed to be associated with the quasi-reversible, two-electron two-proton oxidation of "C=C"group at the side chain of enolic pHPP, and the oxidation process II(a) is proposed to result from the irreversible oxidation of phenolic hydroxyl group. It is observed that in aqueous solution, enolic pHPP can quickly complex with boric acid to yield enol-borate complex that can also oxidize at a glassy carbon electrode to yield an anodic wave. 相似文献
48.
The complexes between R3Tr (Tr = B, Al, and Ga; R = H, F, Cl, and Br) and H2X (X = O, S, and Se) were theoretically studied. The interaction energies of R3Al⋯H2X and R3Ga⋯H2X are consistent with the electronegativity of the halogen atom R (R ≠ H), but an opposite dependence is found for R3B⋯H2X. The triel bond of R3Tr⋯H2X is weaker for the heavier chalcogen donor. The dependence of triel bonding strength on the triel atom is complicated, depending on the nature of R and X. The methyl substitution of H2X causes a substantial increase in the interaction energy from −5.74 kcal/mol to −22.88 kcal/mol, and its effect is relevant to the nature of Tr, X, and R groups. For the S and Se donors, the increased percentage of interaction energy is almost the same due to the methyl substitution, which is larger than that of the O analogue. In most triel-bonded complexes, electrostatic dominates and polarization has comparable contribution. However, polarization plays a dominant role in R3B⋯ and R3B⋯ (R = Cl and Br; R′ = H and Me). 相似文献
49.
50.
Synthesis, structure and magnetic properties of the S=1/2, one-dimensional antiferromagnet, Y5Re2O12
Lisheng Chi 《Journal of solid state chemistry》2003,172(2):451-457
Single crystals of Y5Re2O12 have been grown, and the crystal structure has been determined by X-ray diffraction. This compound crystallizes in space group C2/m with cell dimensions of a=12.4081(10) Å b=5.6604(5)Å, c=7.4951(6) Å, β=107.837(3)°, Z=2. The final refinement led to R1=0.0238, WR2=0.0459 for 1053 observed reflections with F>4σ(F0). Edge-sharing ReO6 octahedra form infinite linear [ReO2O4/2]n chains along the b direction with alternating short and long Re-Re distances. Three crystallographically independent yttrium atoms surround O2 to form OY4 tetrahedra, which share edges and corners in the ab plane to form a two-dimensional Y5O4 network which separates the [ReO2O4/2]n magnetic chains. This compound is therefore isostructural with the series Ln5Re2O12Ln=Gd-Lu, which have been known since 1969. The average Re oxidation state is +4.5 in the chains and a reasonable, if qualitative MO scheme results in one unpaired electron per Re dimer. Consistent with this, magnetic susceptibility data can be fitted to the one-dimensional antiferromagnetic Heisenberg model with S=1/2 and parameters Jintra/k=−89(1)K, g=2.15(4) and χ(TIP)=5(1)×10−4 emu/mol. There is no sign of long-range magnetic order down to 2 K. These results are contrasted with those for the isostructural Y5Mo2O12. 相似文献