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991.
Lin CS Zhang RQ Lee ST Elstner M Frauenheim T Wan LJ 《The journal of physical chemistry. B》2005,109(29):14183-14188
The assembly of small water clusters (H2O)n, n = 1-6, on a graphite surface is studied using a density functional tight-binding method complemented with an empirical van der Waals force correction, with confirmation using second-order M?ller-Plesset perturbation theory. It is shown that the optimized geometry of the water hexamer may change its original structure to an isoenergy one when interacting with a graphite surface in some specific orientation, while the smaller water cluster will maintain its cyclic or linear configurations (for the water dimer). The binding energy of water clusters interacting with graphite is dependent on the number of water molecules that form hydrogen bonds, but is independent of the water cluster size. These physically adsorbed water clusters show little change in their IR peak position and leave an almost perfect graphite surface. 相似文献
992.
Two new compounds from Zingiber officinale 总被引:1,自引:0,他引:1
Yu Zhao Qiao Feng Tao Rong Ping Zhang Chang Xin Zhou Hui Dou Shu Yun Shi Ye Cheng Xiao Lian Li Sun Su Zeng Ke Xin Huang Xiao Dong Zhang Xiao Kun Li 《中国化学快报》2007,18(10):1247-1249
A new cyclic diarylheptanoid,1,5-epoxy-3-hydroxy-1-(3-methoxy-4,5-dihydroxyphenyl)-7-(4-hydroxyphenyl)-heptane (1),as well as a new monoterpene,10-O-β-D-glucopyranosyl-hydroxy cineole (2) were isolated from the rhizomes of Zingiber officinale. The structures of compounds 1 and 2 were established based on their spectral data.In addition,the antioxidant activities of these compounds were also measured. 相似文献
993.
Xi‐Zhao Wang Jiong Jia Yan Zhang Wei‐Ren Xu Wei Liu Fang‐Niu Shi Jian‐Wu Wang 《中国化学会会志》2007,54(3):643-652
The synthesis of a series of new 5‐isoxazolpenicillins is described, which were obtained by coupling substituted isoxazoles with 6‐APA. Concise large‐scale synthesis of 3,5‐disubstituted isoxazoles by 1,3‐dipolar cycloaddition using copper(I) as catalyst was also investigated. Representative compounds were assayed for antimicrobial activities, showing satisfactory antimicrobial activities against Gram‐negative bacteria. 相似文献
994.
The stereochemistry of the hydrogenation of 4-tert-butylmethylenecyclohexane (1) and the use of D2 or D2/H2 mixtures in place of H2 furnishes evidence that hydrogenations using the catalyst precursor [Rh(DIPHOS)(COD)]+BF
4
−
proceed via more than one mechanism. This evidence includes the effect of changes in pressure and added triethylamine upon
the kinetics and isomerization of 1, as well as the distribution of the added deuterium in the products of the reaction of 1 or norbornene with either D2 or H2/D2 mixtures. That an alkene necessarily causes the equilibration of H2/D2 mixtures, although it need not involve any of the alkenes’s hydrogen atoms (e.g., norbornene), provides a clue to the process
by which the mononuclear mechanism proposed by Halpern, which is dominant near one atmosphere of H2, merges into another with increasing pressure. It has been proposed that the cationic complex [Rh(DIPHOS)S2]+ is transformed in the presence of an alkene and hydrogen into a binuclear hydrido complex, such as those described by Sivak
and Muetterties (1979) and Fryzuk (1982), which represent a far more active catalyst than its mononuclear precursor. Such
an intermediate should readily catalyze the H2-D2 equilibration and the isomerization of an alkene in the presence of D2 without necessarily introducing deuterium into the product.
Published in Russian in Kinetika i Kataliz, 2006, Vol. 47, No. 1, pp. 88–97.
Deceased.
The text was submitted by the authors in English.
This work was conducted at the University of Arkansas. 相似文献
995.
Synthetic erythropoietic proteins: tuning biological performance by site-specific polymer attachment
Chen SY Cressman S Mao F Shao H Low DW Beilan HS Cagle EN Carnevali M Gueriguian V Keogh PJ Porter H Stratton SM Wiedeke MC Savatski L Adamson JW Bozzini CE Kung A Kent SB Bradburne JA Kochendoerfer GG 《Chemistry & biology》2005,12(3):371-383
Chemical synthesis in combination with precision polymer modification allows the systematic exploration of the effect of protein properties, such as charge and hydrodynamic radius, on potency using defined, homogeneous conjugates. A series of polymer-modified synthetic erythropoiesis proteins were constructed that had a polypeptide chain similar to the amino acid sequence of human erythropoietin but differed significantly in the number and type of attached polymers. The analogs differed in charge from +5 to -26 at neutral pH and varied in molecular weight from 30 to 54 kDa. All were active in an in vitro cell proliferation assay. However, in vivo potency was found to be strongly dependent on overall charge and size. The trends observed in this study may serve as starting points for the construction of more potent synthetic EPO analogs in the future. 相似文献
996.
Zhengshen Hua Xin Zhang Xiaojing Feng Xiaoran Wang Jun He Xin Wang Huifen Peng 《中国化学快报》2019,30(3):792-796
Ti4+ ions were introduced to the VO43- substituted Li3Fe2(PO4)3 by sol-gel method. Simultaneous substitution of Ti4+ for Fe3+ and VO43- for PO43- in the Li3Fe2(PO4)3 resulted in a net improvement in the rate capability and cycling performance, as compared with the single Ti4+ or VO43- substituted compound. 相似文献
997.
998.
Peter G. Dormer Amude M. Kassim Johnnie L. Leazer Jr. Feng Xu Edward G. Corley Jimmy O. DaSilva David M. Tschaen 《Tetrahedron letters》2004,45(28):5429-5432
A general method for the preparation of syn-2,3-disubstituted-2,3-dihydro-1,4-benzoxathiin rings from 2-mercaptoethanols and quinone ketals is presented. This ring system is produced by Michael addition of a 2-mercaptoethanol to a quinone ketal, followed by cyclization of the initial Michael adduct, and subsequent aromatization to afford a syn-2,3-disubstituted-1,4-benzoxathiin in fair to good chemical yield. Several chiral syn-2,3-disubstituted-2,3-dihydro-1,4-benzoxathiin rings were prepared with this method from enantioenriched 2-mercaptoethanols. No loss of enantiopurity was observed. 相似文献
999.
In earlier work we nave described and partially characterized two histone kinases from regenerating rat liver and other tissues which catalyze the transfer of the γ-phosphoryl group from ATP to histones. The histone phosphates thus formed were observed to be acid-labile and base-stable. In the present study we report on the specificity of one of these enzymes, namely, the kinase which is optimally active at pH 9. This enzyme appears to be relatively specific for the two histidine residues of histone H4. These histidines occur at positions 18 and 75, and both are phosphorylated. However, when regenerating rat liver was the source of enzyme, the product was 1-phosphohistidine, whereas the enzyme from Walker-256 carcinosarcoma catalyzed the formation of 3-phosphohistidine. 相似文献
1000.
复合生物材料的研究进展 总被引:11,自引:0,他引:11
从力学性能的改善和降解速率的可调度等角度,总结了复合生物材料与单一组分的材料相比,在生物医学领域应用中所表现出的综合使用性能的优越性。综述了复合生物材料,特别是用于骨修复的各类有机/无机复合材料近年来的研究进展状况。提出将与人骨中磷灰石微晶类似的羟基磷灰石纳米粒子与可降解聚酯材料进行复合,能够得到具有优越骨诱导性能并且能够降解的新型骨修复材料。这方面的研究代表了有机/无机复合生物材料领域新的发展方向。 相似文献