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991.
V. P. Lesnyak D. I. Shiman L. V. Gaponik F. N. Kaputskii A. I. Lamotkin Zh. V. Bondarenko 《Russian Journal of Applied Chemistry》2007,80(2):295-299
The influence exerted by copolymers of the C9 fraction of liquid pyrolysis products of petroleum raw materials with maleic anhydride and by their esterification products, added to paper pulp, on the main paper properties was examined. 相似文献
992.
F. dall'Acqua S. Caffieri D. Vedaldi A. Guiotto P. Rodighiero 《Photochemistry and photobiology》1983,37(4):373-379
By irradiating (365 nm) an aqueous liquid solution of 4,5'-dimethylangelicin. a monofunctional photosensitizing furocoumarin, in the presence of an excess of thymine, two new compounds, I and II, have been obtained; they do not show fluorescence when observed with Wood's light. The nuclear magnetic resonance data, the marked similarity of UV absorption and fluorescence spectra of these compounds with those of synthetic 3.4-dihydro-4,5'-dimethylangelicin and their capacity to undergo photodissociation (254 nm) yielding the starting thymine and 4,5'-dimethylangelicin in equimolecular amounts, are consistent with C4 -cycloadducts between the 3,4-double bond of the furocoumarin and 5,6-double bond of thymine. Nuclear magnetic resonance data indicate for I and II a head-to-head and a head-to-tail structure, respectively. When irradiation is carried out in the frozen state, two adducts. III and IV, fluorescent at Wood's light, have been obtained other than the two above-mentioned compounds I and II. Compounds III and IV have been identified as 4'.5'-fluorescent adducts between the 4',5'-double bond of the furocoumarin and the 5.6-double bond of thymine; one of them (III) is identical to that formed in the photoreaction between DNA and 4,5'-dimethylangelicin; for this last compound a cis head-to-head structure has been suggested. 相似文献
993.
Tandem purification of mouse IgM monoclonal antibodies produced in vitro using anion-exchange and gel fast protein liquid chromatography 总被引:1,自引:0,他引:1
P Clezardin N R Hunter I R MacGregor J L MacGregor D S Pepper J Dawes 《Journal of chromatography. A》1986,358(1):209-218
A tandem chromatographic procedure was used to isolate rapidly mouse IgM monoclonal antibodies produced by cultivation of hybridomas in vitro. Hybridoma culture supernatants containing mouse IgM monoclonal antibodies were first chromatographed on an anion-exchange Mono Q column connected to a fast protein liquid chromatography system. This anion-exchange step offers the advantage of obtaining IgM antibodies in a concentrated form. The IgM-rich fractions from the Mono Q column were then injected on a gel filtration Superose 6 column equilibrated with a low-ionic strength buffer and eluted with a high-ionic strength buffer. Assessment of the purity of isolated IgM monoclonal antibodies was performed by sodium dodecyl sulphate polyacrylamide gel electrophoresis together with a Coomassie Brillant Blue R 250 staining technique. Assessment of the immunoreactivity of isolated IgM monoclonal antibodies was performed by an enzyme linked immunosorbent assay using a solid phase adsorbed antigen against which IgM monoclonal antibodies were directed. The chromatographic procedures described allows the rapid isolation of mouse IgM monoclonal antibodies produced in vitro at a high degree of purity and in an immunoreactive state. 相似文献
994.
Résumé Les auteurs ont étudié le comportement chromatographique sur plusieurs phases stationnaires polaires et non polaires de composés cyclopropaniques stéréoisomêres: où R=H ou CH3 et X=CH, COOCH3 ou CH2OH. Les résultats sont interprétés en fonction de la configuration de X par rapport à , de la nature électronique de X et de l'orientation du phényle par rapport au plan du cyclopropane.
Relationship between chemical structure and retention. VII. Cyclopropane compounds
Summary The chromatographic behaviour, on several polar and non polar phases, of stereoisomeric cyclopropanes has been studied R=H or CH3 and X=CN, COOCH3, CH2OH. The results are interpreted in terms of the X versus configuration, the electronic nature of X and the orientation of the phenyl ring in relation to plane of the cyclopropane ring.相似文献
995.
D A Richards 《Journal of chromatography. A》1979,175(2):293-299
Electrochemical detection of tryptophan metabolites following separation on a reversed-phase high-performance liquid chromatography column was compared with other means of detection. Of 29 compounds studied, 26 could be detected at a sensitivity comparable to that of fluorescence derivatisation procedures. Response was linear over a wide range of concentrations and selectivity was shown to be superior to ultraviolet detection when analysing urine. Additionally, it was possible to control selectivity so that only those tryptophan metabolites from the tryptophan hydroxylase pathway were detected. This is of particular value in the study of distrubances of serotonin metabolism and is unique to this type of detector. 相似文献
996.
It has been noticed that the major part of the loss of ?H from the molecular ion of most of the o-methoxythioamides results from an ortho effect of the methoxy group. Comparison of the MIKE spectra of the [M? SH]+ of 1-(2-methoxyphenylthioxomethyl)piperidine and 1-(2-methoxyphenylthioxomethyl)pyrrolidine with the MIKE spectra of [M? SH]+ of the corresponding unsubstituted compounds, reported earlier, indicated two parallel pathways for the formation of [M? SH]+ in the o-methoxy compounds. In the first pathway, as has been noticed in thioamides in general, the loss of ?H involves the migration of either the α-hydrogen in the amine moiety or the hydrogen attached to nitrogen. In the second pathway, the migration of a hydrogen from the o-methoxy group to the sulphur atom followed by ejection of SH from the molecular ion leads to a stable cyclized ion. Interesting secondary fragmentations as a consequence of this ortho effect have also been noticed. 相似文献
997.
Summary Thermal decomposition of metal-organic complexes of nickel, cobalt and iron has given catalysts which are very effective at about 900° for the conversion of carbon dioxide, water and other oxygencontaining sample decomposition products to carbon monoxide in the direct determination of oxygen in organic compounds when using a modified Unterzaucher type apparatus. A copper catalyst similarly prepared required a temperature of 1030° whereas a manganese complex decomposition product was ineffective.
Katalysatoren zur Sauerstoffbestimmung in organischen Substanzen
Zusammenfassung Durch thermische Zersetzung metallorganischer Komplexe von Ni, Co und Fe erhält man Katalysatoren, die die Umwandlung von CO2, H2O und anderen sauerstoffhältigen Zerfallsprodukten zu CO bei etwa 900° C bei der direkten Sauerstoffbestimmung in einer modifizierten Unterzaucher-Apparatur sehr wirksam fördern. Ein ähnlich hergestellter Cu-Katalysator erfordert 1030° C und das Zersetzungsprodukt eines Mn-Komplexes ist unwirksam.相似文献
998.
Phlojodicarpin [8-(2,3-epoxy-1-hydroxy-3-methylbutyl)-7-methoxycoumarin, C15H16O5, mp 143–145°C, []
D
25
-37.5°], and isophlojodicarpin [8-(1,2-epoxy-3-hydroxy-3-methylbutyl)-7-methoxycoumarin, C15H16O5, mp 132–134°C, []
D
25
-102.5°] have been isolated from the epigeal part ofPhlojodicarpus sibiricus. The results of the IR, UV, PMR, and mass spectrometry of these compounds are given.Institute of Chemistry, Academy of Sciences of the Mongolian Peoples' Republic, Ulan-Bator. Irkutsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 47–49, January–February, 1981. 相似文献
999.
The structures of three sesquiterpenoids, axisothiocyanate-2(4), axamide-1(5) and axamide-2(6), present in the marine sponge Axinella cannabina, have been determined on the basis of chemical and spectral evidences. 相似文献
1000.
V. V. Korshak S. V. Vinogradova V. A. Vasnev G. D. Markova T. V. Lecae 《Journal of polymer science. Part A, Polymer chemistry》1975,13(12):2741-2749
The effect of conditions of polycondensation on the structure of polymers formed from monomers with symmetric and asymmetric functional groups by nonequilibrium polycondensation has been studied for the system with acceptor-catalytic polyesterification of β-hydroxyethyl ethers of bisphenols and terephthalic acid chloride in the presence of triethylamine. Polymers with statistical or regular arrangement of diol residues in the chain can be produced in such systems, depending on the way in which starting compounds are introduced in the reactor. A difference in the reactivity of functional groups in an asymmetric monomer is not sufficient to produce polycondensation polymers with a regular structure. Gradual introduction of the symmetric monomer is essential to yield polymers with predominant “head-to-head” (“tail-to-tail”) configurations. Some properties of the resulting polymers have been studied. Polymers with ordered residues of the asymmetric monomers in the macromolecules have higher softening temperatures and an increased tendency for crystallization than the statistic polymers. 相似文献