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1.
Analysis and fragmentation mechanisms of hirsutinolide‐type sesquiterpene lactones by ultra‐high‐performance liquid chromatography/electrospray ionization linear ion trap Orbitrap mass spectrometry 下载免费PDF全文
2.
Doris Chen Elizabeth V. Jones Corey W. Williams Tan-Khang N. Huynh Tristan C. McPhail Prof. Dr. Stefan France 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(52):e202201368
Herein, a SnCl4-catalyzed intramolecular, interrupted homo-Nazarov cascade biscyclization to access angular (hetero)aryl-fused polycycles is reported. Subsequent decarboxylation of the readily enolizable products afforded the angular products in up to 71 % yield over two steps, with the trans-diastereomers as the major products. The cyclopropyl homo-Nazarov cyclization precursors were formed using a scalable and modular synthetic route that, ultimately, offers access to 6,6,6-, 6,6,5-, 6,5,6-, 6,6,5,6-, and 6,6,6,5-fused angular polycyclic products. To showcase the rigor and utility of the method, an 8-step total synthesis of (±)-1-oxoferruginol, an antibacterial aromatic abietane diterpenoid, was disclosed. 相似文献
3.
The level structure in neutron-deficient nucleus 91Ru was investigated via the 58Ni(36Ar,2 plnγ)Ru reaction at a beam energy of 111 MeV.Charged particles,neutrons,and y-rays were emitted in this reaction and detected by the DIAMANT CsI ball,Neutron Wall,and the EXOGAM Ge clover array,respectively.In addition to the previously reported levels in 91Ru,new low-to-medium spin states were observed.Angular correlation and linear polarization measurements were performed to unambiguously determine spins and parities of the excited states in 91 Ru.The low-spin states of 91 Ru exhibit a scheme of multi-quasiparticle excitations,which is very similar to that of the neighboring N=47 isotone.These excitations have been interpreted in terms of the shell model.The calculations performed in the configuration space(p3/2,f5/2,p1/2,g9/2)reproduce the experimental excitation energies reasonably well,supporting the interpretation of the newly assigned positive-parity states in terms of the three quasiparticle configurationsπ(g9/2)^-2v(g9/2^-1 and v(g9/2)^-3. 相似文献
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Patrizia Scafato Francesca Caprioli Laura Pisani Daniele Padula Fabrizio Santoro Giuseppe Mazzeo Sergio Abbate France Lebon Giovanna Longhi 《Tetrahedron》2013
Three forms of chiroptical spectroscopies, electronic circular dichroism (ECD), vibrational circular dichroism (VCD), and optical rotatory dispersion (ORD) have been employed to study the configuration and conformational properties of the three molecules: (S)-3-phenylcyclopentanone, (S)-3-phenylcyclohexanone, and (S)-3-phenylcycloheptanone (including (S)-3-phenylcyclopentanone-2,2,5,5-d4 and (S)-3-phenylcyclohexanone-2,2,6,6-d4). ECD and VCD spectra in the mid-IR for the three molecular systems are marginally dependent on fine conformational details, as interpreted in terms of standard DFT computational methods, with common spectroscopic features to the three systems clearly identified. Accounting for vibronic coupling mechanisms reproduces the structuring of ECD n→π∗ band. The ORD curves are quite similar for the three types of molecules, but their interpretation highlights a crucial role played by conformations of the cycloalkanone ring in the case of (S)-3-phenylcycloheptanone. The same conclusions are reached by considering the VCD spectra in the CH-stretching region. 相似文献
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A. Ertoprak B. Cederwall C. Qi M. Doncel U. Jakobsson B. M. Nyakó G. Jaworski P. Davies G. de France I. Kuti D. R. Napoli R. Wadsworth S. S. Ghugre R. Raut B. Akkus H. Al Azri A. Algora G. de Angelis A. Atac T. Bäck A. Boso E. Clément D. M. Debenham Zs. Dombrádi S. Ertürk A. Gadea F. Ghazi Moradi A. Gottardo T. Hüyük E. Ideguchi H. Li C. Michelagnoli V. Modamio J. Nyberg M. Palacz C. M. Petrache F. Recchia M. Sandzelius M. Siciliano J. Timár J. J. Valiente-Dobón Z. G. Xiao 《The European Physical Journal A - Hadrons and Nuclei》2018,54(9):145
8.
J. Großfeld A. Simmer J. van Loon W. Springer S. Juschkewitsch V. Kubelka J. Wagner S. Zuravlev Thompsonwerke W. Normann H. P. Trevithik M. F. Lauro A. Bömer A. Gehrke G. de Belsunce J. I. Lurje F. Fritz Zitek R. Otto A. Halter J. M. Purdy W. G. France W. L. Evans H. P. Kaufmann und M. Keller 《Fresenius' Journal of Analytical Chemistry》1931,83(5-6):223-230
Ohne Zusammenfassung 相似文献
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Boris Brkić Neil France Adam T. Clare Chris J. Sutcliffe Paul R. Chalker Stephen Taylor 《Journal of the American Society for Mass Spectrometry》2009,20(7):1359-1365
In this report, we present a prototype design of a quadrupole mass filter (QMF) with hyperbolic electrodes, fabricated at
the University of Liverpool using digital light processing (DLP), a low-cost and lightweight 3D rapid prototyping (RP) technique.
Experimental mass spectra are shown for H2+, D2+, and He+ ions to provide proof of principle that the DLP mass filter is working as a mass analyzer in the low-mass range (1 to 10
amu). The performance of the DLP QMF has also been investigated for individual spectral peaks. Numerical simulations of the
instrument were performed by coupling CPO and Liverpool QMS-2 programs to model both the ion source and mass filter, respectively,
and the instrument is shown to perform as predicted by theory. DLP thus allows miniaturization of mass spectrometers at low
cost, using hyperbolic (or other) geometries of mass analyzer electrodes that provide optimal ion manipulation and resolution
for a given application. The potential of using RP fabrication techniques for developing miniature and microscale mass analyzers
is also discussed. 相似文献