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1.
The epigeal part ofVerbascum laxum Filar, ét Jav. has yielded in addition to the known sinuatol, a new iridoid glycoside — 6-0-(3-0-p-coumaroyl--L-rhamnopyranosyl)aucubin (I), [] D 20 –174.2±0.7° (c 1.4; MeOH). From the roots of the plant, as the main components giving an iridoid reaction, have been isolated harpagoside and the new iridoid glycoside 6-0-(2,3-di-0-acyl[acetyl,p-methoxy-trans-cinnamoyl]--L-rhamnopyranosyl)aucubin (V) [] D 18 –130±2° (c 0.5; MeOH). The structures of the substances isolated were established with the aid of UV, IR, NMR, and mass spectra.A. L. Mndzhoyan Institute of Fine Organic Chemistry, Academy of Sciences of the Armenian SSR, Erevan. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 90–96, January–February, 1987.  相似文献   

2.
Summary Two new dioximato-bridged trinuclear CrII-CuII-CrIII complexes, [Cr(salen)-Cu(-BD)2-Cr(salen)] (1) and [Cr(salen)-Cu(-FD)2-Cr(salen)]-H2O (2), have been prepared and characterized [salen2– = N,N-ethylene- bis (salicylideneiminate), (-BD)2– = -benzyldioximato and (-FD)2– = -furildioximato]. Magnetic susceptibility measurements in the 4.2–300 K range demonstrated the operation of a ferromagnetic interaction between the adjacent CrIII and CuII ions through oximato bridges in both (1) and (2). Based on spin Hamiltonians =–2J(12+23)(S1=S3=3/2,S2=1/2) the exchange integrals (J) were evaluated as 3.19 and 5.38 cm–1 for (1) and (2), respectively.  相似文献   

3.
    
From the epigeal organs ofSilene scabrifolia Kom. has been isolated the new phytoecdysteroid 2-deoxy--ecdysone 3-acetate (II) (0.0011%), C29H46O6, mp 216–218°, [] D 20 +131.9° (methanol). The enzymatic hydrolysis of (II) led to 2-deoxy--ecdysone (I). The acetylation of 2-deoxy--ecdysone (I) yielded (II) and the 22-monoacetate (III) and 3,22-diacetate (IV) of 2-deoxy--ecdysone, which have been described previously. Details of the IR, UV, CD, mass, and NMR spectra are given for (I) and of the IR, mass, and NMR spectra for (III).Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 439–441, July–August, 1986.  相似文献   

4.
Zusammenfassung Der lineare thermische Ausdehnungskoeffizient von linearem Polyäthylen hoher Dichte wurde im Temperaturbereich –20 °C bis + 40°C bestimmt. Bei isotropen Proben besteht eine lineare Beziehung zwischen Dichte bzw. Kristallisationsgrad v und. Die gemessenen Koeffizienten liegen fürT 0 = 20 °C im Bereich = 110 ... 130 · 10–6 K–1.Kalt verstreckte Proben mit Verstreckungsgraden = 8 ... 15 haben beiT 0 = 20 °C in Verstreckrichtung den Koeffizienten l = –24 · 10–6 K–1. Der negative Zahlenwert von tl ist unabhängig von und weiteren Herstellungsparametern. Seine Ursache ist einerseits die Orientierung derc-Achsen der Kristallite in Verstreckrichtung mit c = –12 · 10–6 K–1 und andererseits der negative Koeffizient am * –50 · 10–6 K–1 der verspannten amorphen Phase, der auf dem gummielastischen Verhalten der tie-molecules beruht.Beim Tempern oberhalb von +40 °C schrumpfen die Proben irreversibel, wobei | ansteigt und nach dem Aufschmelzen der Proben wieder den Wert des isotropen Materials annimmt. Nach dem Tempern wenig unterhalb der Schmelztemperatur der Kristallite wurden überhöhte Koeffizienten | gemessen, die eine Rotation der Kristallite um dieb-Achsen erkennen lassen.
Summary The linear thermal coefficient of expansion,, of high density linear polyethylene has been determined in the temperature range of –20 ° ... + 40 °C. For isotropic samples a linear relationship between density or crystallinity v and is valid. Measured values of forT 0 = 20 °C amount to = 110 ... 130 · 10–6 K–1.Cold drawn samples of draw ratios = 8 ... 15 yield | = –24 · 10–6 K–1 atT 0 = 20 °C parallel to the draw axis. The negative value of | does not depend on draw ratio or other parameters of sample processing. It is caused byc-axis orientation of the crystallites in draw direction with c = –12 · 10–6 K–1 and by a negative coefficient am * = –50 · 10–6 K–1 of the stressed amorphous phase, which is due to rubber elastic behaviour of the tie molecules.When annealed above 40 °C the samples shrink irreversibly and | is augmented. After melting the samples the value of isotropic material is restored. Annealing the samples little below the melting temperature of the crystallites leads to superelevated values all which reflect| rotation of the crystallites around theb-axis.
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5.
From the glycoside fraction of the starfishPatiria pectinifera, after its desulfation, an artefactural glycoside has been obtained: 29(-L-arabinofuranosyloxy)-5-stigmastane-3,6,8,15,16-pentaol (I). The structure of (I) was shown by1H and13C NMR spectra and mass spectra and by acetylation and high-temperature hydrogenation.Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Scientific Center, Academy of Sciences of the USSR, Vladivostok. Institute of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 356–361, May–June, 1985.  相似文献   

6.
By repeated chromatography on Polikhrom-1, silica gel, and Florisil, ethanolic extracts of two species of starfish,Culcita novaeguineae andLinckia guildingi, have yielded the new steroid glycoside culcitoside C1 (I): 5-cholestan-3,4,6,8,15,24-hexaol 24-O-[2,4-di-O-methyl--D-xylopyranosyl-(12)--L-arabinofuranoside], C39H68O14, mp 245–248°C, []D -35.8°, c 0.6; methanol). Its structure was shown by the results of acid hydrolysis, acetylation and methylation, and1H and13C NMR spectroscopy.Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Scientific Center, Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 801–804, November–December, 1985.  相似文献   

7.
A new glycoside — foetoside C — has been isolated from the epigeal part ofThalictrum foetidum L. and, on the basis of chemical transformations and spectral characteristics its structure has been established as oleanolic acid 28-[O--D-glycopyranosyl-(1 6)-O--D-glucopyranoside] 3-O-[O--D-xylopyranosyl-(1 3)-O--L-rhamnopyranosyl-(1 2)--L-arabinopyranoside].Irkutsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 458–463, July–August, 1984.  相似文献   

8.
    
Conclusions We ware the first to obtain,-diphenyl--(2-methylquinoxalyl)hydrazine from,-diphenylhydrazine and 2 -methyl-3-chloromethylquinoxaline.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 695–696, March, 1973.  相似文献   

9.
INAA of Minoan ceramics from Kommos,Crete   总被引:1,自引:0,他引:1  
A recent study concerning the deviation of the E–(1+) epithermal neutron flux distribution from the E–1 law, developed by F. DE CORTE et al. is applied to -determination in different channels of the CRN reactor (Strasbourg). It is found that the coefficient is positive inside the reactor core and negative outside. The accuracy of the neutron activation analysis using the corrected resonance integral I() is tested.  相似文献   

10.
A new alkaloid, which has been called karakanine, has been isolated from the total alkaloids of the epigeal part ofAconitum karakolicum. The structure of karakanine as 8,14-dihydroxy-16-methoxy-4-methyl-N-ethyl-1,19-epoxyaconitane has been proposed on the basis of a study of its IR, PMR, mass, and13C NMR spectra, and has been confirmed by its conversion into karakoline.Institute of Chemistry of Plant Substances, Uzbekistan Republic Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedeninii, No. 1, pp. 62–64, January–February, 1993.  相似文献   

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