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801.
Dmitrenok A. S. Radhika P. Anjaneyulu V. Subrahmanyam C. Subba Rao P. V. Dmitrenok P. S. Boguslavsky V. M. 《Russian Chemical Bulletin》2003,52(8):1868-1872
Sphingolipids and glycolipids including previously unknown (2S,3S,4R)-1,3,4-trihydroxy-2-(2-(R)-hydroxyoctadecanoylamino)octadec-8E-ene, (2S,3R)-1,3-dihydroxy-2-octadecanoylamino-4E,8E-hexadecadiene, and (2-hydroxy-3-hexadecyloxypropyl)--L-fucopyranoside were isolated from soft corals collected on the shelf near the Andaman Islands (Indian Ocean). The structures of all compounds were established by spectroscopic methods and chemical analyses. The lipids possessed antibacterial activity against Bacillus subtilis, Bacillus pumilus, Escherichia coli, and Pseudomonas aeruginosa and antifungal activity against Aspergillus niger, Rhizopus oryzae, and Candida albicans. 相似文献
802.
Rao PV Bhaduri S Jiang J Hong D Holm RH 《Journal of the American Chemical Society》2005,127(6):1933-1945
The construction of a synthetic analogue of the A-cluster of carbon monoxide dehydrogenase/acetylcoenzyme synthase, the site of acetylcoenzyme A formation, requires as a final step the formation of an unsupported [Fe(4)S(4)]-(mu(2)-SR)-Ni(II) bridge to a preformed cluster. Our previous results (Rao, P. V.; Bhaduri, S.; Jiang, J.; Holm, R. H. Inorg. Chem. 2004, 43, 5833) and the work of others have addressed synthesis of dinuclear complexes relevant to the A-cluster. This investigation concentrates on reactions pertinent to bridge formation by examining systems containing dinuclear and mononuclear Ni(II) complexes and the 3:1 site-differentiated clusters [Fe(4)S(4)(LS(3))L'](2-) (L' = TfO(-) (14), SEt (15)). The system 14/[{Ni(L(O)-S(2)N(2))}M(SCH(2)CH(2)PPh(2))](+) results in cleavage of the dinuclear complex and formation of [{Ni(L(O)-S(2)N(2))}Fe(4)S(4)(LS(3))]- (18), in which the Ni(II) complex binds at the unique cluster site with formation of a Ni(mu(2)-SR)(2)Fe bridge rhomb. Cluster 18 and the related species [{Ni(phma)}Fe(4)S(4)(LS(3))](3)- (19) are obtainable by direct reaction of the corresponding cis-planar Ni(II)-S(2)N(2) complexes with 14. The mononuclear complexes [M(pdmt)(SEt)]- (M = Ni(II), Pd(II)) with 14 in acetonitrile or Me(2)SO solution react by thiolate transfer to give 15 and [M(2)(pdmt)(2)]. However, in dichloromethane the Ni(II) reaction product is interpreted as [{Ni(pdmt)(mu(2)-SEt)}Fe(4)S(4)(LS(3))](2-) (20). Reaction of Et(3)NH(+) and 15 affords the double cubane [{Fe(4)S(4)(LS(3))}(2)(mu(2)-SEt)](3-) (21). Cluster 18 contains two mutually supportive Fe-(mu(2)-SR)-Ni(II) bridges, 19 exhibits one strong and one weaker bridge, 20 has one unsupported bridge (inferred from the (1)H NMR spectrum), and 21 has one unsupported Fe-(mu(2)-SR)-Fe bridge. Bridges in 18, 19, and 21 were established by X-ray structures. This work demonstrates that a bridge of the type found in the enzyme A-clusters is achievable by synthesis and implies that more stable, unsupported single thiolate bridges may require reinforcement by an additional covalent linkage between the Fe(4)S(4) and nickel-containing components. (LS(3) = 1,3,5-tris((4,6-dimethyl-3-mercaptophenyl)thio)-2,4,6-tris(p-tolylthio)benzene(3-); L(O)-S(2)N(2) = N,N'-diethyl-3,7-diazanonane-1,9-dithiolate(2-); pdmt = pyridine-2,6-methanedithiolate(2-); phma = N,N'-1,2-phenylenebis(2-acetylthio)acetamidate(4-); TfO = triflate.). 相似文献
803.
L. F. Brum Malta Marta Eloisa Medeiros 《Journal of Thermal Analysis and Calorimetry》2005,81(1):149-152
Summary This work reports the room-temperature stabilization of the Bi4V2-xFexIIO11-1.5x γ ‘ phase, a promising ionic conductive material that finds application in solid oxide fuel cell and oxygen sensor devices. The Fe(II) cation proved to be a better stabilizer than Fe(III), which was previously used, since a lower substitution degree of V5+ is needed for the former. Powder X-ray diffraction, Fourier-transform infrared spectroscopy and differential scanning calorimetry were used in these experiments. 相似文献
804.
H. R. Veenendaal P. M. van Berkel G. de Jong P. K. Baggelaar 《Accreditation and quality assurance》2007,12(7):365-368
Due to the relatively large spread in the results of microbiological proficiency tests, the z-scores are often not able to detect zero or low results as being ‘bad’ results. This paper describes an adapted z-score based on the average or the standard deviation of the 50% ‘highest’ results. The combination of the adapted z-scores of four samples enables a better judgement of the performance of each laboratory.
Papers published in this section do not necessarily reflect the opinion of the Editors, the Editorial Board or the Publisher. 相似文献
805.
Thermal decomposition of strontium titanyl oxalate tetrahydrate and calcium titanyl oxalate hexahydrate have been studied employing TG, DTA, gas and chemical analysis. The decompositions proceed through three major steps: dehydration, decomposition of the oxalate to a carbonate and the decomposition of the carbonate to yield the final products, the metatitanates. The intermediates of the oxalate decomposition are found to be Sr2Ti2O4+x(CO3)2-x(CO2)x and Ca2Ti2O4(CO3)2, respectively. The entrapment of carbon dioxide in the former and the presence of non-equivalent carbonate groups in the latter are substantiated by their i.r. spectra. The penultimate solid residues are poorly crystalline Sr2Ti2O5CO3 and amorphous Ca2Ti2O5CO3. Decompositions of these carbonates are accompanied by growth in particle size of the products, SrTiO3 and CaTiO3, respectively. 相似文献
806.
Hans König 《Analytical and bioanalytical chemistry》1973,266(2):119-124
The separation of a mixture of 22 bactericides has been achieved by gas chromatography on columns with silicone rubber W-982 as stationary phase with temperatures between 100° and 300°C. The unchanged compounds as well as their silylation products have been used. The latter are more conveniently used especially for the quantitative determination. To be able to calculate the retention indices after Kovats gas chromatography has been performed isothermally at 180°C for the more volatile compounds and at 250°C for all other bactericides.The retention indices obtained under these conditions are tabulated together with the limits of detection. 相似文献
807.
Valérie Chevalier-Billosta Jean-Paul Joseleau Alain Cochaux Katia Ruel 《Cellulose (London, England)》2007,14(2):141-152
The composition and ultrastructural arrangement of cell wall polymers in wood fibres have determining influence on the properties
of wood derived materials. It is therefore important to improve our understanding of the relationship between fibres organisation,
the modifications induced by pulping treatments, and the resulting paper sheet mechanical properties. The different treatments
to which fibres are subjected during the manufacturing of pulps and papers induce morphological and micro-structural alterations
due to the removal of wall constituents and of microfibrillar elements. The impact of pulping processes on fibres was investigated
at the ultrastructural scale of transmission electron microscopy. Particular attention was given to the effects of beating
in refiners at various intensities on the ultrastructure of fibres. The most characteristic effects consisted of delaminations,
microfibril disorganisation, and even fractures, of varying importance depending on the intensity of the mechanical refining.
The consequences of internal alterations and surface modifications of the fibres were examined in relation to the paper sheet
mechanical properties. Correlations between the type of alteration observed in the fibres and its possible impact on a given
paper mechanical property are suggested. With similar approaches, the effects of drying and recycling were studied. 相似文献
808.
Stereoselectivity of reductive amination of (R)-1-hydroxy-1-phenylpropan-2-one by methylamine was studied. From the four isomers possible, only two are produced by this
reaction. These are marked as (−)-(1R,2S)-ephedrine (desired product) and (+)-(1S,2R)-ephedrine. The reaction stereoselectivity depends both on the type of the catalyst and reaction conditions. The most suitable
type is the supported platinum. However, this catalyst rapidly deactivates. With a decreasing activity of Pt catalyst, the
stereoselectivity decreases. It is also decreased during the production of the second liquid phase (water) in the reaction
mixture. 相似文献
809.
Y. X. Xia J. I. Friese D. A. Moore P. P. Bachelor L. Rao 《Journal of Radioanalytical and Nuclear Chemistry》2007,274(1):79-86
The complexation of plutonium(IV) with sulfate at variable temperatures has been investigated by solvent extraction method.
A NaBrO3 solution was used as holding oxidant to maintain the plutonium(IV) oxidation state throughout the experiments. The distribution
ratio of Pu(IV) between the organic and aqueous phases was found to decrease as the concentrations of sulfate were increased.
Stability constants of the 1:1 and 1:2 Pu(IV)-HSO4
− complexes, dominant in the aqueous phase, were calculated from the effect of [HSO4
−] on the distribution ratio. The enthalpy and entropy of complexation were calculated from the stability constants at different
temperatures using the Van’t Hoff equation. 相似文献
810.
Gabriela Flores-Ramírez Manuel Rivera Alfredo Morales-Pablos Joel Osuna Xavier Soberón Paul Gaytán 《BMC chemical biology》2007,7(1):1