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991.
Summary 1. The solid-phase method of peptide synthesis has been used to obtain the heptapeptide HGly-L-Ala-L-Phe-L-Val-Gly-L-Leu-L-Met which is an analog of eledoisin.2. The possibility has been shown of using o-nitrophenylsulphenyl derivatives of amino acids in the solid-phase method of peptide synthesis.Khimiya Prirodnykh Soedinenii, Vol. 2, No. 3, pp 200–202, 1966 相似文献
992.
A. A. Kiryushkin V. I. Shchelokov V. K. Antonov Yu. A. Ovchinnikov M. M. Shemyakin 《Chemistry of Natural Compounds》1967,2(4):224-229
Summary 1. A method for the separation and quantitative determination of - and -DNP derivatives of , -DABA, ornithine, and lysine has been proposed.2. A quantitative evaluation of the N N migration in four peptides of , -DABA has been carried out.3. The degree of migration in inactive polymyxin M and the DNP-peptides from a partial hydrolyzate of the inactivated antibiotic has been determined.4. The amino acid composition of the DNP peptide B1 from a partial hydrolyzate of active DNP-polymyxin M has been established.5. The quantitative aspect of the conversion of
and
diketopiperazines has been studied.Khimiya Prirodnykh Soedinenii, Vol. 2, No. 4, pp. 277–284, 1966 相似文献
993.
A. G. Kotov Yu. A. Breslav S. Ya. Pshezhetskii 《Theoretical and Experimental Chemistry》1969,5(3):236-239
The adsorption of the paramagnetic molecules of NO and NO2 by zeolites in the alkali and alkaline earth cationic forms has been studied by EPR and reflectance spectroscopic methods. The change in the EPR spectra of adsorbed nitric oxide with increase in the degree of covering of the surface of the alkali cationic form of the zeolites, and also the nature of the change in the spectra when oxygen is adsorbed on zeolites on which NO has previously been adsorbed, indicate the existence of two types of adsorption center. At low degrees of covering of the surface, on the order of 1018 g–1, as can be judged from the EPR spectra, the adsorbed NO molecule is strongly polarized and the unpaired electron is almost completely localized on the oxygen atom. At high degrees of covering, for an appreciable proportion of the NO molecules, the bond with the surface is weaker. In this case, the EPR spectra show a hyperfine structure (HFS) with a constant which changes with change in the cation in the order Li+ Na+ K+. The replacement of the singly charged Na+ by the doubly charged Ca2+ produces a marked change in the adsorption properties of the zeolite. The adsorption of NO on CaA leads not only to polarization of the adsorbed molecule but also to transfer of the electron from the nitrogen atom to the atoms of the adsorbent; this is recorded in the EPR spectrum in the form of an F-center. On further adsorption, the NO molecules are adsorbed both on the nitrogen atom and on the oxygen atom of the first molecule; thus, NO2 and N2O are formed. 相似文献
994.
S. V. Litvinenko Yu. M. Volovenko F. S. Babichev 《Chemistry of Heterocyclic Compounds》1993,29(2):194-199
The reaction of -substituted 2-quinoxalylacetonitriles with 1-alkyl(aryl)imidazoles, -benzimidazoles, -1,2,4-triazoles and 5,6-dihydroimidazo[i,j]quinoline was studied. It was found that during the course of the reaction an unusually easy dealkylation of the azole ring takes place, while the aryl substituent is not split off. A reaction mechanism has been proposed including the formation of an ylide intermediate, followed by subsequent electrophilic attack on the C(2) position of the azolium ring. The applicability boundaries of the reaction studied and the spectral characteristics of the synthesized compounds were investigated.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 224–229, February, 1993. 相似文献
995.
Summary DSC data on crystallization kinetics from the melt at different cooling rates of nylon 6 containing various amonts of untreated and surface-treated fillers, were analyzed in terms of a modified Kolmogorov-Avrami equation. It was established that mechanism of crystallinity development in molten nylon 6 does not change appreciably in presence of aminosilane-treated glass beads and small amounts of untreated glass beads, whereas time exponentn was found to decrease with increasing filler content in samples containing untreated glass beads and Aerosil. On the other hand, dependence of temperature of the onset of crystal nucleation on cooling rate obeyedm = 2 law for pure nylon 6 and samples containing surface-treated filler, whilem = 4 law seemed to hold for samples containing large amounts of untreated fillers at low cooling rates (m is the exponent at degree of supercooling). It was concluded that although isothermal conditions of crystallization should be preferred for further quantitative investigations of polymer-filler interactions in highly filled polymer melts, the above results qualitatively are consistent with trends discovered in isothermal crystallization experiments. 相似文献
996.
997.
Yu. P. Egorov G. I. Derkach A. A. Kisilenko A. S. Tarasevich 《Theoretical and Experimental Chemistry》1972,5(5):403-408
The UV and IR absorption spectra and the NMR and NQR spectra of certain isocyanates of three- and four-coordinated phosphorus have been investigated. The reciprocal effect of the phosphorus atom and the NCO group is discussed on the basis of spectral analysis, quantum chemical calculations of the electron systems, and calculations of the normal vibrational forms. Comparison of the (PO) frequencies in the IR spectra of the phosphorus isocyanates with the Taft gives a linear relationship which testifies to the predominant inductive effect of the NCO group on the P(O)R1R2 grouping. A similar relationship is observed between the resonance frequency res in the NMR spectra and for C1P(O)R1R2 compounds. The effect of the phosphorus atom on the electronic system in the NCO group is shown by the hypsochromic shift of the absorption band in the210-m region and an appreciable increase in its intensity, compared with alkyl isocyanates. This fact, which agrees with the NMR spectral data and the quantum chemical calculations, indicates the presence of conjugation in the P-N bond. We found the order of the P-N bond to be approximately 1.2. This partial double-bond nature of the P-N bond results from the interaction of the p electrons of nitrogen in the NCO group with the d orbitals of the phosphorus atom.We are grateful to our colleagues at the Kazan Physicotechnical Institute AS USSR A. I. Rivkind, S. G. Salikhov, and I. A. Safin for recording the spectra. 相似文献
998.
Extraction of californium/III/ from aqueous pyrophosphate and tripolyphosphate solutions with D2EHPA
V. Chakravortty S. A. Perevalov Yu. M. Kulyako 《Journal of Radioanalytical and Nuclear Chemistry》1989,136(2):85-94
Extraction of californium/III/ with di-/–2-ethylhexyl/ phosphoric acid /D2EHPA/ in heptane from pyrophosphate media is almost quantitative between pH 4 and 5. From tripolyphosphate media, however, two to three extractions are needed in the pH range of 3–5 to isolate Cf3+ completely. Reextraction experiments show that 1M H2SO4 can back-extract Cf3+ completely while two to three reextractions with 5M HNO3 can only separate californium/III/. Reverse phase partition chromatography experiments were performed to recover 300 g of californium/III/. From slope analysis of the extraction data the composition of the extracted species has been found to be Cf/H2P2O7/A.HA and Cf/H4P3O10/.A2.2HA from pyrophosphate and tripolyphosphate solutions, respectively, where D2EHPA is abbreviated as /HA/2. 相似文献
999.
1000.
在非水溶剂(二甲基亚砜(DMSO)及N,N_二甲基甲酰胺(DMF))中的伏安曲线.呈现三对电流峰,表明存在三个可逆或准可逆酞菁配体的单电子转移过程,而在水溶液中则不呈现准可逆行为,且波形改变很大.此外,还比较了四磺酸基酞菁锌的水溶液在自然光和红光(600~700nm)照射下的循环伏安曲线,其氧化还原峰的数目和峰电位基本不变,但在红光照射下比自然光照射下的峰电流明显增大. 相似文献