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11.
12.
Charles L. Watkins Larry K. Krannich Colacot J. Thomas Dileep Srivastava 《Polyhedron》1994,13(24):3299-3307
The reactions of (Me2AlH)3 with Me2AsNMe2, MeAs(NMe2)2, and As(NMe2)3 were investigated as a function of time at room temperature and over the temperature range −90 to 24°C by use of 1H and 13C NMR spectroscopy. (Me2AlH)3 was found to be very reactive toward the aminoarsines, even at −90°C, and no stable Me2AlH-aminoarsine adducts were observed. Instead, the initial stages of the reactions involved AS---N bond cleavage with the generation of highly reactive AlN- and AsH-bonded species. The subsequent course of each reaction and the final arsenic-containing product distribution depended upon the original AL:N stoichiometric ratio and the respective aminoarsine. When the Al:N ratio was 1:1, the reactions were straightforward for each aminoarsine. However, in every case, [Me2AlNMe2]2 was the final AlN-containing product. Independent reactions were carried out to verify many of the proposed decomposition pathways that lead to thermodynamically stable products. The results of this study are compared with those of the analogous, previously reported (Me3Al)2-aminoarsine systems. Additionally, a new synthetic route to [Me2AlAsMe2]3 has been established from the reaction of (Me2AlH)3 with Me2AsH. 相似文献
13.
14.
G. Lhersonneau D. Weiler P. Kohl H. Ohm K. Sistemich R. A. Meyer 《Zeitschrift für Physik A Hadrons and Nuclei》1986,323(1):59-67
An isomeric state at 3,523 keV excitation energy in97Y with a half-life of 144(10) ms has been discovered with the fission-product separator JOSEF. This isomer is depopulated through aγ transition of 162 keV. AnE3 multipolarity for this transition is consistent with the measured conversion coefficients ofα K =0.98(20) andα T =1.00(19). Subsequent electromagnetic transitions populate several new97Y levels which have high spins. For the isomer the three-quasiparticle configuration [πg 9/2?ν(h 11/2,g 7/2)]27/2? is proposed. TheE3 transition with a strength about 2 single-particle units is supposed to be of the typeh 11 2/+1 →d 5 2/?1 . These findings provide evidence for the rapid shape transition atA?100 since they indicate shell-model character of 39 97 Y58 even at high excitation energies while the immediate neighbour 39 98 Y59 contains a rotational band based on a level at 495 keV. 相似文献
15.
Coated-wire ion-selective electrodes based on dinonylnaphthalene sulfonic acid (DNNS) are prepared for methadone, methylamphetamine, cocaine and protriptyline in protonated form. In each set, nearly-Nernstian responses are obtained while detection limits range from 10-5.5M for cocaine and methylamphetamine electrodes, to 10-6.0M for methadone, and 10-6.5 M for protriptyline electrodes. Selectivity is found to decrease in the order methadone, protriptyline, cocaine and methylamphetamine; these results are consistent with systematic selectivity studies reported earlier for electrodes in this family. 相似文献
16.
The characterization of the compounds CF3SeX (X = H, Cl, Br, CN, CF3, SeCF3) is completed by the report of melting points, boiling points, enthalpies of vaporization and entropies of vaporization. Ultraviolet and mass spectra are presented and discussed. An improved synthesis for CF3SeH is reported. 相似文献
17.
The relative intensities and energy separation of allowed EPR lines of a paramagnetic species and partially forbidden spin flip satellite lines due to dipole-dipole coupling between the paramagnetic species and the matrix nuclei have been analyzed in a new way. The analysis allows one to determine both the distance to and the number of matrix nuclei that contribute to a given satellite transition. For hydrogen atoms trapped in a gamma-irradiated sulphuric acid glass at 77 K the analysis indicates that interaction occurs with four matrix protons at a distance of 2.15 Å. For trapped hydrogen atoms in phosphoric acid glass the analysis indicates interaction with four matrix protons at 2.37 Å. 相似文献
18.
D ← X resonance enhanced three-photon excitation spectrum of iodine was observed by a cw intracavity absorption technique. Vibrational quantum numbers of D ← X transitions are given for every major spectral feature. The corresponding one-photon enhancement from the B state is evident from the one-photon vibrational assignment. The spectroscopic constants for the D state are v00 = 40 998 cm?1 ω′0 = 113 cm?1 and ω′0χ′0 = 0.045 cm?. 相似文献
19.
[reaction: see text] The enediamine tautomer of a variety of substituted amidine free bases reacts with nitric oxide (NO) to produce compounds containing a carbon-bound diazeniumdiolate [R1R2R3C-N(O)=NO-] functional group (previously called "nitrosohydroxylamines"). The new reaction has been shown to be quite general, although the nature of the products does vary. Amidines containing more than one replaceable hydrogen produce polydiazeniumdiolates as intermolecular salts, while those in which only one diazeniumdiolation can occur provide zwitterionic salts. These diazeniumdiolated amidines are shown to be useful NO donor compounds which undergo very slow spontaneous dissociation on dissolution in pH 7.4 phosphate buffer to produce mixtures of NO and nitrous oxide containing mostly NO. The most advantageous manifestation of the new discovery is the preparation of the monodiazeniumdiolated amidine zwitterions. Reaction of the medically relevant alpha-adrenergic agonists tetrahydrozoline and idazoxan produced monodiazeniumdiolated amidine zwitterions from which NO release was observed for up to 28 days and showed little sign of ending. The reaction should be applicable to a variety of pharmaceutical agents, including NO synthase inhibitors, antitumor agents, and antibacterials. 相似文献
20.
James Y. Becker Larry L. Miller Frank R. Stermitz 《Journal of Electroanalytical Chemistry》1976,68(2):181-191
The electrochemical oxidation of the alkaloid laudanosine (Ia) to O-methylflavinantine (II) has been studied in acetonitrile solvent. Using cyclic voltammetry, rotating disc voltammetry and preparative electrolyses on several alkaloids, simple aliphatic amines and aromatic compounds, some aspects of the mechanism of this coupling reaction are elucidated. The first anodic wave for laudanosine at platinum has Ep=0.55 V vs. Ag/Ag+. The electrode rapidly becomes partially passivated at potentials above 0.5 V. This is due to a film which “dissolves” below 0.5 V, at a rate independent of the potential. It is shown that the reaction (Ia)→(II) proceeds at 0.5 V by initial oxidation of the amine moiety. If acids such as sodium bicarbonate are added to the anolyte the amine is protonated causing the first wave to disappear. Oxidation at 1.1 V under these acidic conditions produces the same product, but more rapidly and in significantly higher yield because electrode filming and side reactions resulting from the amine oxidation are abrogated. 相似文献