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91.
92.
蒙旦树脂化学组成的研究 总被引:7,自引:5,他引:7
采用阴离子交换色谱和硅胶-氧化铝柱色谱对云南寻甸蒙旦树脂(XDSZ)、潦浒蒙旦树脂(LHSZ)、昭通蒙旦树脂(ZTSZ)和吉林舒兰蒙旦树脂(SLSZ)进行了族组分的分离。树脂游离酸,树脂结合酸,树脂烃和树脂醇在各树脂中的百分含量分别为XDSZ11.86,8.76,12.30,45.99;LHSZ15.89,13.91,4.90,45.99;SLSZ25.46,8.07,17.40,36.22;ZT 相似文献
93.
Fashui?HongEmail author Xuefeng?Wang Chao?Liu Guoxing?Su Weiping?Song Kang?Wu Ye?Tao Guiwen?Zhao 《中国科学B辑(英文版)》2003,46(1):42-50
It was studied by spectroscopy that PSII reaction center complex consisting of three polypeptides, D1, D2 and Cytb559, were purified from PSII particle of CeCl3 treated spinach. The results of the experiment show that Ce3+ could improve the growth of spinach, and accelerate electron transport of PSII particles. Of chl-a of UV-Vis spectrum of
D1/D2/Cytb559 complex, Soret band was blue-shifted by 3 nm and Q band by 2 nm, respectively, and the fluorescence emission
peak was blue-shifted by 5 nm in CeCl3-treated spinach compared with the one in control. By the extended X-ray absorption fine structure (EXAFS) spectroscopy methods,
it has been found that Ce3+ is coordinated with 8 nitrogen atoms in the first coordination shell with Ce-N bond length of 0.253 nm, and Ce3+ with 6 oxygen atoms in the second coordination shell with Ce-O bond length of 0.32 nm. However, the secondary structure of
D1/D2/Cytb559 complex by circular dichroism (CD) spectroscopy has no significant change after CeCl3 treated. It might be that Ce3+ binds to porphyrin rings of chlorophyll and oxygen of amino acid residue of polypeptide in D1/D2/Cytb559 complex, and then
accelerates the primary reaction of PSII, intensifies function of P680+ primary electron donor of D1/D2/Cytb559, but there is little change in conformation of PSII reaction center complex. 相似文献
94.
A. Bershadskii 《Journal of statistical physics》1994,77(3-4):909-914
Corrections of Batchelor's spectral law –1 of passive scalar-fluctuations are obtained by taking into account the topological instabilities of small-scale vortex sheets: –4/3 for supercritical and –5/4 for subcritical regimes. The corresponding fractal dimensions of the scalar interface areD
=8/3 for supercritical andD
=11/4 for subcritical regimes. Good agreement with experimental data is established. 相似文献
95.
Alain Joye 《Journal of statistical physics》1994,75(5-6):929-952
The spectrum of the Floquet operator associated with time-periodic perturbations of discrete Hamiltonians is considered. If the gap between successive eigenvalues
j
of the unperturbed Hamiltonian grows as
j
-
j-1
j
and the multiplicity of
j
grows asj
with >0 asj tends to infinity, then the corresponding Floquet operator possesses no absolutely continuous spectrum provided the perturbation is smooth enough. 相似文献
96.
97.
D. N. Kravtsov A. S. Peregudov L. S. Golovchenko E. I. Smyslova 《Russian Chemical Bulletin》1996,45(5):1194-1199
19F NMR spectroscopy was used to study the exchange reactions involving 4-fluorothiophenoxides, 4-nitrophenoxides, chlorides, and acetates of arylmercury and triphenylphosphinegold. The analysis of the data on equilibrium constants allows one to obtain information on the comparative chemical hardness of ArHg+ and Ph3PAu+ cations. The increase in the electron-donating ability of aryl ligands enhances the chemical hardness of ArHg+ cations, their influence being best described by 0 constants of substituted phenyl groups.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1255–1260, May, 1996. 相似文献
98.
K. Premchand B. Seetharami Reddy B. Mallikarjuna Rao K. Parthasaradhi M. V. R. Murti K. S. Rao 《Il Nuovo Cimento D》1993,15(1):73-76
Summary An attempt is made to study theK
α
L
1 satellite multiplet structure of chlorine atoms in different compounds by photon excitation. A comparison of the averageK
α
L
1 group energy shift from the diagram line with those based on Dirac-Fock evaluations with different number ofM-shell electrons shows a reasonable agreement. The
intensity ratios are found to be higher than those studied in Mg compounds in general. 相似文献
99.
100.
Gong WT Li XC Ning GL Zhu L Wang L Lin Y 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,62(4-5):835-839
Two novel phenylated pyrylium compounds, silver (I)-bridged 2,3,4,5-tetraphenylpyrylium perchlorate (P1) and its silver (I)-free pyrylium ligand (P2) were prepared from 1,2,3,4-tetraphenylcyclopentadiene to examine their spectroscopic behaviors. The UV/vis absorption and fluorescent emission spectra of P1 and P2, measured in three solvents (acetonitrile, dichloromethane and toluene), reveal that the photophysical behaviors are closely related to silver (I) fragment, and strongly dependent on solvent polarity. In polar acetonitrile, P1 displays longer absorption wavelength and much lower fluorescent emission intensity than P2, although they exhibit much similarity in shape. In contrast, in nonpolar toluene, while P2 shows an apparent absorption band at 338 nm, P1 displays a tail-like line without absorption band observed. All the spectra obtained indicate a better coplanarity and a stronger intra-molecular charge transfer in P1 due to the effect of silver (I) fragment. Additionally, the 1H NMR spectra of P1 and P2, which were recorded under the same conditions, indicate that the silver (I) fragment reinforces pyrylium ring's capacity to localize the formal positive charge within the heterocyclic ring. 相似文献