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881.
Akisada H Kuwahara J Koga A Motoyama H Kaneda H 《Journal of colloid and interface science》2007,315(2):678-684
The critical micelle concentrations (CMC) of binary mixtures of alkyltrimethylammonium bromides (CnTAB) were measured by a conductivity method. The CMCs of C12TAB-C14TAB and C14TAB-C16TAB systems exhibit the usual behavior, namely a monotonic decrease of the CMC with the mole fraction of the longer chain surfactant. However, the CMC behaviors of C10TAB-C16TAB, C11TAB-C16TAB, C12TAB-C16TAB, and C11TAB-C14TAB are unusual. The behaviors of the CMCs with mole fraction for these systems consist of three regions, of which the first is characterized by a very small decrease of the CMC in the range of low mole fraction, followed by a second where there is an abrupt decrease of the CMC, and a third where the CMCs exhibit their usual behavior. The molecular interaction parameter omega is almost equal to zero for mixtures that have the usual CMC behavior, but is small and positive for those systems with unusual CMCs. We infer that for very low mole fractions of C16TAB, the C16TA ion in the C12TAB-C16TAB system penetrates imperfectly into the micelle and its two methylene groups exist outside the micelle. 相似文献
882.
883.
Benten H Guo J Ohkita H Ito S Yamamoto M Sakumoto N Hori K Tohda Y Tani K 《The journal of physical chemistry. B》2007,111(37):10905-10914
Intermoiety electronic interactions in the singlet and triplet excimer states of triply bridged [3.3.n](3,6,9)carbazolophanes ([3.3.n]Cz, n=3-6) were studied by emission and transient absorption measurements. In these [3.3.n]Cz molecules, the dihedral angle and the separation distance r between fully overlapped two carbazole rings change systematically from nearly parallel (n=3, r=3.35 A) to oblique (n=6, r=4.03 A). In rigid glass at 77 K, [3.3.n]Cz (n=3, 4) (r<4 A) exhibited red-shifted and structureless excimer fluorescence and phosphorescence while [3.3.n]Cz (n=5, 6) (r>4 A) exhibited monomer-like vibrational fluorescence and phosphorescence. In solution at 130 K, all [3.3.n]Cz molecules exhibited an excimeric fluorescence band while [3.3.5]Cz still exhibited monomer-like phosphorescence. Transient absorption spectra measured at 294 K exhibited local excitation and charge-transfer bands for all [3.3.n]Cz molecules in the excited singlet and triplet states, suggesting that not only singlet but also triplet excimers of carbazole are formed at room temperature. Furthermore, the singlet-triplet energy gap decreased with the decrease in n, suggesting that electrons are effectively delocalized over the two carbazole moieties. These findings showed that both singlet and triplet excimers of carbazole are formed with a separation distance shorter than about 4 A and are most stable in the parallel-sandwich structure and that the configurational mixing between exciton resonance and charge resonance states plays an essential role in the formation of singlet and triplet excimers of carbazole. 相似文献
884.
Maeda Y Yamauchi H Fujisawa M Sugihara S Ikeda I Aoshima S 《Langmuir : the ACS journal of surfaces and colloids》2007,23(12):6561-6566
Hydration changes of poly(2-methoxyethyl vinyl ether) (PMOVE) synthesized via living cationic polymerization have been investigated during a temperature-responsive phase separation in water by using infrared spectroscopy. An aqueous PMOVE solution has lower critical solution temperatures (LCSTs) of 66 degrees C in H2O and 65 degrees C in D2O at approximately 15 wt %. During phase separation, the C-H stretching (nu(C-H)) bands of PMOVE shift downward (red shift). In particular, the IR band assigned to the antisymmetric stretching vibration of the terminal methyl groups exhibits a remarkably large red shift by 16 cm-1. The band also exhibits a red shift with increasing polymer concentration at T < Tp. Density functional theory (DFT) calculations of the models of hydrated PMOVE indicate that the shift is due mainly to the breaking of hydrogen bonds (H-bonds) between the oxygen of the methoxy groups and water and partially to the breaking of the CH...O H-bond to them. 相似文献
885.
Bis(disulfide)bridged Nb(+4) cluster halide complexes [Nb2S4X8]4– (X = Cl, Br) were prepared by acid hydrolysis of [Nb2S4(NCS)8]4– in concentrated aqueous HCl or HBr, solution from which they can be isolated as double salts Cs5[Nb2S4X8]X (X = Cl, 1 ; X = Br, 2 ). The crystal structures of 1 and 2 were determined. The isolation and X-ray structure of oxonium salt (H3O)5 [Nb2S4Cl8]Cl ( 3 ) is also reported. 1 – 3 contain new [Nb2S4X8]4– anions which can also be viewed as excised building blocks of polymeric solids NbS2X2. The extra halogen resides in the center of octahedron formed by six Cs+ or H3O+ ions. All the three salts are isostructural and crystallize in tetragonal space group Immm with the following parameters: a = 10.269(2), b = 16.343(2), c = 7.220(1) Å for 1 , a = 10.934(1), b = 16.613(2), c = 7.470(1) Å for 2 , a = 9.639(1), b = 16.031(1), c = 7.071(1) Å for 3 . The parameters of the Nb2S4 core are only slightly affected by the change from Cl to Br. 相似文献
886.
Yoichi Takanishi Hideo Takezoe Yoshiichi Suzuki Ichiro Kobayashi Tomoko Yajima Masahiro Terada Koichi Mikami 《Angewandte Chemie (International ed. in English)》1999,38(16):2353-2356
Right- and left-handed homochiral domains segregate in a fluid smectic phase of the racemic (R*,S*)-β-Me-TFMHPOBC analogue shown. This CF3-containing liquid crystalline compound exhibits an electrooptic response in a homogeneous cell, although no macroscopic dipole is expected to exist. Moreover, the homeotropic cells of this material exhibit striped domains, which are associated with fine stripes having two opposite tilt senses with respect to the predominant stripes. 相似文献
887.
888.
889.
Shigeki Habaue Hiroshi Sakamoto Hideo Baraki Yoshio Okamoto 《Macromolecular rapid communications》1997,18(8):707-713
Optical resolution of ethylenebis(4,5,6,7-tetrahydro-1-indenyl) complexes of zirconium and hafnium was performed by using cellulose tris(3,5-dimethylphenylcarbamate) coated on silica-gel (Chiralcel OD) as a chiral stationary phase for HPLC. The biphenyl-2,2′-diolate complexes were completely resolved with the highest separation factor. The isolated enantiomerically pure hafnocenes were applied for the asymmetric cyclopolymerization of 1,5-hexadiene. 相似文献
890.
A simple method for evaluating the molecular electrostatic potential (MEP) map without self-consistent field molecular orbital (SCF-MO) calculation is extended, and the parameters for amino acids, peptides, and proteins are determined. In this method, the electrostatic potentials due to electrons in the valence shells are calculated by a set of simple empirical functions at various origins, and those due to the core electrons and nuclei by point charge approximation. For application of the method to amino acids, peptides, and proteins, the functions for the σ and π bonds and lone-pair electrons involved in these species were determined, and the MEP maps calculated by the empirical functions were compared with those calculated by an ab initio method. It is shown that the method reproduces correctly the shape of ab initio MEP map even for the repulsive MEP region. The method is shown to be very useful for rapid evaluation of reliable MEPs for large biological molecules. © 1996 by John Wiley & Sons, Inc. 相似文献