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991.
992.
Ioan Nanu Constantin Andrei 《Journal of polymer science. Part A, Polymer chemistry》1974,12(1):231-240
Research was carried out on copolymerization of isoprene with maleic acid monoesters in the presence of free radicals (AIBN). The aim of the study was to observe the effect of the different monoesters obtained with normal alcohols of the aliphatic series: monoethyl maleate, monopropyl maleate, monobutyl maleate, monoheptyl maleate, monolauryl maleate, and monocetyl maleate. On the basis of reactivity ratios determined by the Fineman-Ross method and compared with the Mayo-Lewis method, all the systems studied are typical cases of heterocopolymerization. The parameter r1 is constant for this homologous series with the exception of the low terms. The experimental results agree with the ultimate model equation (with deviation at very high values of [M10]/[M20]), but not with the copolymer composition equation which considers the effect of the penultimate unity (penultimate model). Characterization of the sequential distribution is also presented (considering the effect of the terminal group only), and deviations of the experimental results are also discussed. 相似文献
993.
Astashkin AV Feng C Raitsimring AM Enemark JH 《Journal of the American Chemical Society》2005,127(2):502-503
A 17O ESEEM investigation of the high pH form of chicken sulfite oxidase using hyperfine sublevel correlation (HYSCORE) spectroscopy at 29.25 GHz has revealed a new type of exchangeable 17O ligand that is characterized by a significantly smaller hyperfine interaction ( approximately 5 MHz) than that previously detected by CW EPR. This new type of exchangeable oxygen ligand is assigned to the axial oxo group of the Mo(V) center. 相似文献
994.
Demirdöven N Cheatum CM Chung HS Khalil M Knoester J Tokmakoff A 《Journal of the American Chemical Society》2004,126(25):7981-7990
We investigate the sensitivity of femtosecond Fourier transform two-dimensional infrared spectroscopy to protein secondary structure with a study of antiparallel beta-sheets. The results show that 2D IR spectroscopy is more sensitive to structural differences between proteins than traditional infrared spectroscopy, providing an observable that allows comparison to quantitative models of protein vibrational spectroscopy. 2D IR correlation spectra of the amide I region of poly-l-lysine, concanavalin A, ribonuclease A, and lysozyme show cross-peaks between the IR-active transitions that are characteristic of amide I couplings for polypeptides in antiparallel hydrogen-bonding registry. For poly-l-lysine, the 2D IR spectrum contains the eight-peak structure expected for two dominant vibrations of an extended, ordered antiparallel beta-sheet. In the proteins with antiparallel beta-sheets, interference effects between the diagonal and cross-peaks arising from the sheets, combined with diagonally elongated resonances from additional amide transitions, lead to a characteristic "Z"-shaped pattern for the amide I region in the 2D IR spectrum. We discuss in detail how the number of strands in the sheet, the local configurational disorder in the sheet, the delocalization of the vibrational excitation, and the angle between transition dipole moments affect the position, splitting, amplitude, and line shape of the cross-peaks and diagonal peaks. 相似文献
995.
Choukourov A Biederman H Slavinska D Hanley L Grinevich A Boldyryeva H Mackova A 《The journal of physical chemistry. B》2005,109(48):23086-23095
Plasma polymerization of allylamine is performed both in continuous wave and pulsed mode. Chemical derivatization is applied to determine primary and secondary amine concentration. Primary amines are efficiently formed, but secondary amines are more abundant. A polymerization mechanism is proposed to account for the difference in amine content obtained from comparison between continuous wave and pulsed mode plasma polymerization. The AFM measurements performed on ultrathin (1-10 nm) plasma polymers confirm the continuity of films and that the film growth on silicon occurs via a layer-by-layer mechanism because no islandlike structures were detected. 相似文献
996.
Dmitri Mitcov Mikhail Platunov Christian D. Buch Anders Reinholdt Anders R. Dssing Fabrice Wilhelm Andrei Rogalev Stergios Piligkos 《Chemical science》2020,11(31):8306
Magnetochiral dichroism (MΧD) originates in the coupling of local electric fields and magnetic moments in systems where a simultaneous break of space parity and time-reversal symmetries occurs. This magnetoelectric coupling, displayed by chiral magnetic materials, can be exploited to manipulate the magnetic moment of molecular materials at the single molecule level. We demonstrate herein the first experimental observation of X-ray magnetochiral dichroism in enantiopure chiral trigonal single crystals of a chiral mononuclear paramagnetic lanthanide coordination complex, namely, holmium oxydiacetate, at the Ho L3-edge. The observed magnetochiral effect is opposite for the two enantiomers and is rationalised on the basis of a multipolar expansion of the matter–radiation interaction. These results demonstrate that 4f–5d hybridization in chiral lanthanoid coordination complexes is at the origin of magnetochiral dichroism, an effect that could be exploited for addressing of their magnetic moment at the single molecule level.Magnetochiral Dichroism of chiral mononuclear lanthanoid complexes is for the first time detected by X-ray absorption measurements on single crystals of Holmium oxydiacetate, at the Ho L3-edge. The effect is of opposite sign for the two enantiomers. 相似文献
997.
Michael Finkelberg Victor Ginzburg Andrei Ionov Alexander Kuznetsov 《Selecta Mathematica, New Series》2016,22(4):2491-2534
We study the natural Gieseker and Uhlenbeck compactifications of the rational Calogero–Moser phase space. The Gieseker compactification is smooth and provides a small resolution of the Uhlenbeck compactification. We use the resolution to compute the stalks of the IC-sheaf of the Uhlenbeck compactification. 相似文献
998.
999.
Andrei Neguţ 《Letters in Mathematical Physics》2016,106(9):1265-1316
We prove the connection between the Nekrasov partition function of \({\mathcal{N}=2}\) super-symmetric U(2) gauge theory with adjoint matter and conformal blocks for the Virasoro algebra, as predicted by the Alday–Gaiotto–Tachikawa relations. Mathematically, this is achieved by relating the Carlsson–Okounkov Ext vector bundle on the moduli space of rank 2 sheaves with Liouville vertex operators. Our approach is geometric in nature, and uses a new method for intersection-theoretic computations of the Ext operator. 相似文献
1000.
Dr. Andrei S. Batsanov Prof. Dr. Javier A. Cabeza Dr. Marco G. Crestani Dr. Manuel R. Fructos Dr. Pablo García‐Álvarez Dr. Marie Gille Prof. Zhenyang Lin Prof. Dr. Todd B. Marder 《Angewandte Chemie (International ed. in English)》2016,55(15):4707-4710
Many transition‐metal complexes and some metal‐free compounds are able to bind carbon monoxide, a molecule which has the strongest chemical bond in nature. However, very few of them have been shown to induce the cleavage of its C?O bond and even fewer are those that are able to transform CO into organic reagents with potential in organic synthesis. This work shows that bis(pinacolato)diboron, B2pin2, reacts with ruthenium carbonyl to give metallic complexes containing borylmethylidyne (CBpin) and diborylethyne (pinBC≡CBpin) ligands and also metal‐free perborylated C1 and C2 products, such as C(Bpin)4 and C2(Bpin)6, respectively, which have great potential as building blocks for Suzuki–Miyaura cross‐coupling and other reactions. The use of 13CO‐enriched ruthenium carbonyl has demonstrated that the boron‐bound carbon atoms of all of these reaction products arise from CO ligands. 相似文献