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11.
12.
《Magnetic resonance in chemistry : MRC》2003,41(2):139-142
Bioassay‐guided fractionation of the methanol extract of Odontadenia macrantha afforded a new limonoid, odontadenin A (1) and two known triterpenoids, lupeol (2) and α‐amyrin (3). The structure of 1 was established on the basis of 1D and 2D NMR and high‐resolution fast atom bombardment mass spectrometric data. The new compound was found to possess moderate cytotoxicity against A2780, the ovarian cancer cell line. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
13.
Using the multipoles method, we formulate the problems of radiation (both heave and sway) of water waves by a submerged sphere
in deep as well as in uniform finite depth water with an ice-cover, with the ice-cover being modelled as an elastic plate
of very small thickness. In each case this leads to an infinite system of linear equations which are solved numerically by
standard techniques. The added-mass and damping coefficients for a heaving and swaying sphere are obtained and depicted graphically
against the wave number for various values of the radius of the submerged sphere and flexural rigidity of the ice-cover to
show the effect of the presence of ice-cover on these quantities. When the flexural rigidity is taken to be zero, the numerical
results for the added-mass and damping coefficient for water with a free surface are recovered. 相似文献
14.
Stefanie M. Walz Thomas E. Malner Ulrich Mueller Rolf Muelhaupt 《Journal of Polymer Science.Polymer Physics》2003,41(4):360-367
We explored phase separation and self‐assembly of perfluoroalkyl segments at the surface of polymer films obtained from latices of semifluorinated acrylate copolymers and the corresponding latex blends of nonfluorinated and semifluorinated polyacrylates. With laser‐induced secondary mass spectrometry the fluorine distribution was measured after annealing above the minimum film‐forming temperature of the polymers up to a depth of several micrometers. Depth profiles of a semifluorinated acrylate homopolymer and latex blends thereof with fluorine‐free alkylacrylates with 25, 50, and 75 mol % semifluorinated acrylate as well as a copolymer comprised of alkyl acrylate and semifluorinated acrylate (50/50 mol %) were investigated. In the case of latex blends containing both semifluorinated polyacrylates and fluorine‐free or low‐fluorine polymers, self‐assembly accounted for enrichment of the perfluoroalkyl segments at the surface. Coatings exhibiting low surface energy and having a substantially reduced total fluorine content were obtained. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 360–367, 2003 相似文献
15.
Sridevi Kaiti Eric Fossum 《Journal of polymer science. Part A, Polymer chemistry》2006,44(6):2099-2106
A thorough study of the polymerization behavior of 4‐fluoro‐4′‐hydroxytriphenyl‐phosphine oxide, 2 , under nucleophilic aromatic substitution reactions has been carried out. The synthesis of 2 was achieved in excellent yields by the reaction of bis(4‐fluorophenyl)phenylphosphine oxide, 1 , with one equivalent of potassium hydroxide in DMSO/water. The structure and purity of 2 were confirmed via 1H, 13C, and 31P NMR spectroscopy along with elemental analysis. Polymerization reactions of 2 in NMP or DMSO at 180 °C provided the corresponding linear poly(arylene ether phosphine oxide)s, PAEPOs, with number average molecular weights, Mn, ranging from 11,700 to 36,500 Da. All of the polymer samples were completely soluble in chloroform, tetrahydrofuran, DMSO, NMP, and DMAc. The polymerization reactions were accompanied by a competing intramolecular process that resulted in the formation of cyclic oligomeric species that were removed via a final precipitation from methanol. Analysis using 31P NMR spectroscopy and size exclusion chromatography (SEC) confirmed that the majority of the lower molecular weight cyclic species were removed via this process. The polymer samples formed tough films when chloroform solutions were slowly evaporated on a glass slide. The PAEPO samples prepared in this study exhibited excellent thermal stability with Td (5%) values between 503 and 542 in air while the glass transition temperatures ranged from 223 to 237 °C. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2099–2106, 2006 相似文献
16.
Conditions for the formation of rare earth element (Y, La–Lu) 3-methylglutarates were studied and their quantitative composition
and solubilities in water at 293 K were determined (10–2 mol dm–3). The IR spectra of the prepared complexes with general formula Ln2(C6H8O4)3
nH2O (n=3–8) were recorded and their thermal decomposition in the air were investigated. During heating the hydrated 3-methylglutarates
are dehydrated in one step and next anhydrous complexes decompose to oxides Ln2O3 with intermediate formation Ln2O2CO3 (Y, La, Nd–Gd) or directly to the oxides, Ln2O3, CeO2, Pr6O11 and Tb4O7 (Ce, Pr, Tb–Lu).
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
17.
Far-IR absorption and reflection spectra, as well as laser Mandelshtam–Brillouin and Raman scattering spectra of -glycine, β-alanine,
-histidine,
-tryptophane single crystals in the 0.2–400 cm−1 range were investigated. It was revealed that the far-IR and Raman spectra of the amino acids under study contain more bands than predicted by factor-group analysis, thus indicating a possible contribution of low-energy intramolecular vibrations and overtones, as well as an emergence of forbidden vibrations. Some of the low-frequency bands have never, to our knowledge, been detected previously. 相似文献
18.
Liu H Hu Y Yang S Guo W Lu X Zhao L 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(21):6392-6406
We report herein a comprehensive study of photoinduced reactions in complexes of Mg+ with primary (n-propyl- and isopropylamine) and secondary amines (dipropyl- and diisopropylamine) in the spectral range of 230-440 nm. Similar to the methyl- and ethylamine complexes studied previously, N-H bond activation of these complexes is very unfavorable. Instead, the C(alpha)-C, C-N, and C(alpha)-H bond-cleavage photoproducts are observed after photoexcitation of the Mg+ complexes (3(2)P<--3(2)S). For Mg+(primary amine) complexes, for example, Mg+-NH2CH2CH2CH3, and Mg+-NH2CH(CH3)2, the photoproducts resulting from C(alpha)--C rupture prevail after P(z) and charge-transfer excitations, whereas the Mg+ photofragment is predominant upon P(x,y) excitation. However, with further N-alkyl substitution, as in Mg+(secondary amine) complexes, for example, Mg+-NH(CH2CH2CH3)2 and Mg+-NH[CH(CH3)2]2, a novel intracomplex C-C coupling photoreaction dominates on P(x,y) excitation of Mg+, which is believed to arise from Mg+* insertion into the C-N bond. With P(z) and charge-transfer excitation, the Mg-R elimination photoproducts, arising from C(alpha)-C bond cleavage, predominate. The energetics and possible mechanisms of the intracomplex photoreactions are analyzed in detail with the help of extensive quantum mechanics calculations. 相似文献
19.
L.A. Leites A.V. Zabula S.S. Bukalov A.A. Korlyukov P.S. Koroteev O.S. Maslennikova M.P. Egorov O.M. Nefedov 《Journal of Molecular Structure》2005,750(1-3):116-122
Vibrational (Raman and IR) spectra of the 1:1 complexes of dihalogermylene and dihalostannylene with 1,4-dioxane and PPh3 have been reported, the structures of the complexes Cl2Ge·C4H8O2 and Cl2Ge·PPh3 updated using high-resolution X-ray method. Quantum-chemistry calculations of the geometry and normal mode frequencies and eigenvectors were carried out for some of the complexes. The results show that in the structure of the polymeric solid complexes of X2M with 1,4-dioxane, intermolecular coordination XM plays a prominent role, whereas the corresponding complexes with PPh3 are monomeric. In the vibrational spectra of all the complexes, an inversion of symmetric and antisymmetric stretching νXM (X=Cl, Br; M=Ge, Sn) frequencies, found for ‘free’ X2MII particles, still persists, suggesting that the X2M moieties preserve their specifity as carbene analogues also in the complexes. 相似文献
20.
A. S. Tatikolov Kh. S. Dzhulibekov Zh. A. Krasnaya E. V. Grechkina V. I. Avdeeva V. A. Kuz'min 《Russian Chemical Bulletin》1992,41(11):1985-1991
The absorption spectra of a number of cationic-anionic polymethine dyes in polar, low-polarity, and nonpolar solvents were studied. It was established that in polar solvents the absorption spectra represent the sum of the absorption spectra of the cation and anion, whereas in nonpolar and low-polarity solvents, in many cases the appearance of a short-wave absorption band is observed, due to interaction of the chromophores of the cation and anion in ion pairs. In solvents of intermediate polarity (for example, in chloroform and ethyl acetate), a concentration dependence of the absorption spectra is observed, determined by the equilibria of ionic dissociation. The ionic dissociation constants of a number of cationic-anionic dyes in chloroform and ethyl acetate were determined by a conductometric method. The thermodynamic data obtained are compared with the spectral data.N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences, 117977 Moscow. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 11, pp. 2524–2532, November, 1992. 相似文献