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11.
The structure, vibrational spectra and electronic properties of the neutral, singly and doubly charged C52 fullerenes were studied by means of the Hartree-Fock method and density functional theory. Different isomers were considered, in particular those with the lowest possible number (five or six) of adjacent pentagons, and an isomer with a four-atom ring. For neutral and singly charged species, the most stable isomer is that with the lowest number of adjacent pentagons, namely five. However, for C(52)2+, the most stable structure has six adjacent pentagons. This finding, which contradicts the pentagon adjacency penalty rule, is a consequence of complete filling of the HOMO pi shell and the near-perfect sphericity of the most stable isomer. The simulated vibrational spectra show important differences in the positions and intensities of the vibrations for the different isomers. 相似文献
12.
Computer modelling of the conformational equilibrium of 2-and 2,5,5-substituted 1,3,2-dioxaborinanes
V. V. Kuznetsov O. Yu. Valiakhmetova S. A. Bochkor 《Chemistry of Heterocyclic Compounds》2007,43(12):1577-1581
Empirical, semiempirical, and nonempirical quantum-chemical methods were used to study the conformational equilibrium of 2,5,5-substituted
1,3,2-dioxaborinanes. The sofa invertomers were found to correspond to the local and global minima on the potential energy
surface. The position of the equilibrium between these forms is a function of the substituents at C(5) of the heterocycle.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1860–1865, December, 2007. 相似文献
13.
Mark Salomon 《Journal of solution chemistry》1990,19(12):1225-1236
Conductivity data are used to determine thermodynamic complex formation constants for cases in which both the initial electrolyte and the complexed electrolyte form ion pairs. Using the method described in the text, the complex formation constants of Li+, Na+ and K+ with the crown ether 18-crown-6 and of Li+ with the ligand triphenylphosphine oxide in propylene carbonate have been evaluated from conductance data. The complexation of AgBr in propylene carbonate solutions of n-etrabutylammonium bromide has also been studied by the measurement of molar conductivities. The results of these studies indicate that ion pairing should not be neglected, even in high permittivity solvents such as propylene carbonate, and that the ion pair association constants correlate well with structural studies on cation-crown ether molecular conformations. 相似文献
14.
V. I. Kovalenko L. I. Maklakov E. I. Borisoglebskaya L. I. Potapova E. A. Shokova I. M. Vatsouro V. V. Kovalev 《Russian Chemical Bulletin》2007,56(6):1103-1109
Based on the Fourier transform IR spectroscopy together with the published NMR and X-ray data, it was shown that cyclic co-operative
intramolecular hydrogen bond in calix[n]arene (n = 4, 6, 8) molecules is mainly responsible for their conformational state irrespective of the presence or absence of bulky
substituents at the upper rim of the molecules. In accordance with the size of a macrocycle (n = 4, 6, 8), the stable conformation, secured by such a hydrogen bond, constitutes a cone, a pinched cone, and a pleated loop, respectively. The new, potentially competing system of hydrogen bonds in calix[6]arenes with 3-carboxymethyl-1-adamantyl
substituents does not affect the conformational state of the macrocycle and its H-bonding. Six carboxy groups at the upper
rim form in pairs three cyclic dimers, which does not disturb the hydrogen bonds of the hydroxy groups and the conformation
of the macrocycle. In addition, the cavity of the molecule is considerably enlarged. The removal or rearrangement of the guest
molecules in the solid calixarene by heating up to 180 °C only slightly affects the conformational state of macrocycles bearing
bulky substituents, whereas in calixarenes devoid of such substituents, the similar procedure leads to somewhat of a distortion
of the macrocycles (judging from the IR spectral indications of hydrogen bonding).
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1062–1068, June, 2007. 相似文献
15.
Amorphous, nanocrystalline, and bulk AlO(OH) · xH2O crystals have six fundamental modes (FM) of vibration in a nonlinear AlO(OH) molecular structure. Most of them appear in groups of four IR and Raman bands. Their positions and relative intensities differ significantly in three specimens. The nanocrystals (monoclinic structure with z=8 molecules per unit cell) have four OH stretching bands at values enhanced by up to 360 cm−1 at 3120, 3450, 3560 cm−1 in comparison to those in bulk crystals or amorphous specimens. The first two bands are broad, bandwidth Δν1/2200 to 350 cm−1, while the other two are sharp, Δν1/290 cm−1. The sharp bands shift to 3525 and 3595 cm−1 after heating the sample at 100°C. They no longer appear after heating at 300 or 500°C for 2 h (the specimen decomposes to Al2O3), leaving behind only two bands at 3100 and 3400 cm−1. A Δν1/2 value of 500 cm−1 appears in the 3400 cm−1 in a delocalized distribution of H atoms. Two bands also occur at 3098 and 3300 cm−1 in bulk crystals (orthorhombic structure with z=4) or at 2990 and 3515 cm−1 in an amorphous sample. More than one bands appear in a FM vibration in occurrence of sample in more than one conformers. The amorphous sample has approximately the same conformer structure as the bulk crystals. An amorphous surface structure exists in nanocrystals with a group of three bands at 1420, 1510 and 1635 cm−1 in an interconnected network structure. It encapsulates the nanocrystals in an amorphous shell. Its volume fraction, 33% estimated from the integrated intensity in three bands, determines 2.2 nm thickness in the shell in spherical shape of nanocrystals in 35 nm diameter. 相似文献
16.
Stereoisomers of 1,5,6,7(H)- and 1,5,6,7(H)-guai-11(13)-en-6,12-olides are calculated using molecular mechanics. The possibility of forming various conformations in the 7-membered ring is examined as a function of the fusion to the 5-membered C-ring. The effect of the methyl orientation on the conformation of the 7-membered ring and the relative stability of the conformers are discussed.Insitute of Phytochemistry, Karaganda, fax (3212)-43-37-73. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 54–56, January–February, 2000. 相似文献
17.
The structures, energies, and natural atomic charges of 2-dimethylaminophenol oxide, 2-Me2N-(O)C6H4OH, and 2-dimethylphosphinylphenol, 2-Me2P(O)C6H4OH, in three different conformations were computed at the ab initio MP2/6-31G* level. Computed natural charges indicate distributions of electron density in amine oxides and phosphine oxides that are quite different from what is normally assumed on the basis of the formal charges in the usual representations of these compounds. The charges on nitrogen and phosphorus in these compounds are typically computed to be approximately zero on nitrogen and +2 on phosphorus, and the oxygen is considerably more negative in the phosphine oxide than in the amino oxide. Electronegativity differences thus play a larger role and formal charges a smaller one in determining atomic charges in these compounds than is generally believed. Despite the more negative oxygen in phosphine oxides, amine oxides are computed to be considerably more basic when participating in hydrogen bonding. Calculations treating the computed natural charges on these six conformations as point charges for classical approximations of the coulombic energies support the idea that the quantum mechanically computed relative energies are largely determined by coulombic interactions. 相似文献
18.
Iva Movre Šapić Vesna Volovšek Krešimir Furić Lahorija Bistričić Vladimir Dananić 《Macromolecular Symposia》2011,305(1):122-125
In this work we investigated the solidification of aminopropylsilanetriol dissolved in water (∼25%) under different conditions by Raman spectroscopy. The solidification was carried out at three different temperatures 8 °C, 23 °C and 60 °C. The influence of electromagnetic radiation on the polymerization process was also studied. Samples were held to solidify in dark and at UV (254 nm and 356nm) spectral range. In order to investigate the influence of the substrate on the resulting polymer structure, teflon, PVC, glass, brass and silica were used. Best ordered polymerized structure was achieved for samples deposited on plastics and solidified in dark, at room temperature. 相似文献
19.
Mariela M. Nolasco Ana M. Amado Paulo J. A. Ribeiro‐Claro 《Journal of Raman spectroscopy : JRS》2009,40(4):394-400
A computationally‐assisted methodology to assign the vibrational spectra of molecular materials (PiMM) has been successfully applied to the Raman and infrared (IR) spectra of trans‐cinnamic acid (t‐CIA) in the solid state. The effects of molecular association through O H···O hydrogen‐bonding in both the wavenumber and the intensity of the bands are accurately described by a single dimer structure. This supports the discrimination between the possible conformers in the solid, the complete evaluation of hydrogen‐bonding effects, and the full assignment of the vibrational spectra of t‐CIA. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
20.