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41.
G. Benzoni F. Azaiez S. Leoni S. Battacharyya R. Borcea A. Bracco L. Corradi D. Curien G. De France Zs. Dombrádi E. Fioretto S. Franchoo S. Grevy F. Ibrahim S. Iulian G. Mukherjee A. Navin G. Pollarolo N. Redon P. H. Regan M. Rejmund C. Schmitt G. Sletten D. Sohler M. Stanoiu S. Szilner D. Verney 《The European physical journal. Special topics》2007,150(1):83-86
A study of deep-inelastic and multi-nucleon transfer reactions to populate neutron-rich
O, Ne and F nuclei is here presented. The reaction under analysis employed a beam of radioactive
24Ne at 7.9 AMeV, provided by the
SPIRAL facility at Ganil, impingin on a 208Pb target. The reaction products have been
detected in the VAMOS spectrometer in coincidence with gamma rays
measured by the EXOGAM array. Preliminary results here presented show a selectivity
in the population of states of different nature. 相似文献
42.
The structure of trans‐[Cr(Me2tn)2Cl2]2ZnCl4 (Me2tn = 2,2‐dimethylpropane‐1,3‐diamine) was determined by a single‐crystal X‐ray diffraction study at 173 K. The analysis reveals that there are three crystallographically independent chromium(III) complex cations in the title compound. The chromium(III) atoms are coordinated by four nitrogen atoms of Me2tn and two chlorine atoms in a trans arrangement, displaying a distorted octahedral geometry. The two six‐membered chelate rings in three complex cations are oriented in an anti chair–chair conformation with respect to each other. The Cr–N and Cr–Cl bond lengths average 2.0862(2) and 2.3112(6) Å, respectively. The ZnCl42– have slightly distorted tetrahedral arrangement with Zn–Cl lengths and the Cl–Zn–Cl angles are influenced by hydrogen bonding. The resolved absorption maxima in the electronic d–d spectrum were fitted with a secular determinant for a quartet energy state of the d3 configuration in a tetragonal field. It is confirmed that the nitrogen atoms of the Me2tn ligand are strong σ donors, but the chloro ligands have weak σ‐ and π donor properties toward the chromium(III) ion. 相似文献
43.
P. Leone 《Fresenius' Journal of Analytical Chemistry》1926,69(10):407-408
Ohne Zusammenfassung 相似文献
44.
R. Benedikt F. Ulzer Focke Finkener Th. Morawski Alfred H. Allen O. Schweissinger R. Marzahn Dieterich Hazura F. W. A. Woll Bruno Röse Ch. Dubois L. Padé R. Bensemann Audoynaud Levallois T. Leone A. Longi F. Benecke Joseph Herz P. Soltsien C. Schädler C. L. Reimer W. Will und H. Hager 《Fresenius' Journal of Analytical Chemistry》1888,27(1):524-539
Ohne Zusammenfassung 相似文献
45.
Complex tripodal tris(2-aminoethyl)amine (tren)-based ligands have been prepared in a single-pot reaction of tren with 3 equiv each of cyclohexenone and a benzaldehyde derivative (i.e., from seven components and three molecular types). The highest yield of product was obtained for p-nitrobenzaldehyde, the most electrophilic aldehyde used. 相似文献
46.
John M. Leone 《国际流体数值方法杂志》1990,11(7):969-984
This paper presents a detailed numerical solution to a simplified version of two-dimensional stratified flow over a backward-facing step with a Froude number of 16/9, a Reynolds number of 800 and a Prandtl number of 1—one of the Open Boundary Condition Symposium test problems. The steady state solution was derived by integrating the time-dependent Boussinesq equations forward in time using a semi-implicit finite-element-based model on a 38400-element mesh. In addition to presenting the results derived on this grid, the paper also presents the results of a Richardson extrapolation calculation for a set of ‘key’ parameters. It is hoped that this solution can be used as a baseline to compare the performance of the various techniques discussed at the Open Boundary Condition Symposium. 相似文献
47.
Meade Bolton C. Kraus T. Leone Link Heraeus Flügge A. Pfeiffer E. Esmarch Carl Fränkel von Sehlen's M. Hochstetter G. Bischof Alex Köbrich O. Kasper Dupré Joseph Klein John Henry Smith J. W. Mallet's E. Reichardt Mayrhofer Leopold Spiegel Katharine J. Williams W. Ramsay A. B. Cooper Baeseler Nobbe Will W. Knop C. W. Heaton Thomas Stevenson Odling Tidy Crookes P. T. Austen Austen und Francis A. Wilber 《Fresenius' Journal of Analytical Chemistry》1888,27(1):77-84
Ohne Zusammenfassung 相似文献
48.
A. M. Stefanini Jincheng Xu L. Corradi G. Montagnoli H. Moreno Y. Nagashima L. Mueller M. Narayanasamy D. R. Napoli P. Spolaore S. Beghini F. Scarlassara G. F. Segato F. Soramel C. Signorini H. Esbensen S. Landowne G. Pollarolo 《Physics letters. [Part B]》1990,240(3-4):306-310
Elastic scattering angular distributions have been measured for 58Ni+64Ni at three energies around the Coulomb barrier employing a new kinematic coincidence technique. The data are compared with the results of coupled-channels calculations including inelastic excitations as well as one-and two-neutron transfer reactions. The agreement is good and the calculations also agree well with the available transfer and fusion reaction data. 相似文献
49.
Zhanghua Zeng Dr. Angel A. J. Torriero Dr. Alan M. Bond Prof. Leone Spiccia Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(30):9154-9163
The [Fc? bis{ZnII(TACN)(Py)}] complex, comprising two ZnII(TACN) ligands (Fc=ferrocene; Py=pyrene; TACN=1,4,7‐triazacyclononane) bearing fluorescent pyrene chromophores linked by an electrochemically active ferrocene molecule has been synthesised in high yield through a multistep procedure. In the absence of the polyphosphate guest molecules, very weak excimer emission was observed, indicating that the two pyrene‐bearing ZnII(TACN) units are arranged in a trans‐like configuration with respect to the ferrocene bridging unit. Binding of a variety of polyphosphate anionic guests (PPi and nucleotides di‐ and triphosphate) promotes the interaction between pyrene units and results in an enhancement in excimer emission. Investigations of phosphate binding by 31P NMR spectroscopy, fluorescence and electrochemical techniques confirmed a 1:1 stoichiometry for the binding of PPi and nucleotide polyphosphate anions to the bis(ZnII(TACN)) moiety of [Fc? bis{ZnII(TACN)(Py)}] and indicated that binding induces a trans to cis configuration rearrangement of the bis(ZnII(TACN)) complexes that is responsible for the enhancement of the pyrene excimer emission. Pyrophosphate was concluded to have the strongest affinity to [Fc? bis{ZnII(TACN)(Py)}] among the anions tested based on a six‐fold fluorescence enhancement and 0.1 V negative shift in the potential of the ferrocene/ferrocenium couple. The binding constant for a variety of polyphosphate anions was determined from the change in the intensity of pyrene excimer emission with polyphosphate concentration, measured at 475 nm in CH3CN/Tris‐HCl (1:9) buffer solution (10.0 mM , pH 7.4). These measurements confirmed that pyrophosphate binds more strongly (Kb=(4.45±0.41)×106 M ?1) than the other nucleotide di‐ and triphosphates (Kb=1–50×105 M ?1) tested. 相似文献
50.
C. Curceanu M. Bazzi G. Beer L. Bombelli A. M. Bragadireanu M. Cargnelli G. Corradi A. d??Uffizi C. Fiorini T. Frizzi F. Ghio B. Girolami C. Guaraldo R. S. Hayano M. Iliescu T. Ishiwatari M. Iwasaki P. Kienle P. Levi Sandri A. Longoni V. Lucherini J. Marton S. Okada D. Pietreanu K. Piscicchia M. Poli Lener T. Ponta A. Rizzo A. Romero Vidal A. Scordo H. Shi D. L. Sirghi F. Sirghi H. Tatsuno A. Tudorache V. Tudorache O. Vazquez Doce E. Widmann J. Zmeskal 《Few-Body Systems》2011,50(1-4):447-449
The DA??NE electron?Cpositron collider at the Laboratori Nazionali di Frascati of INFN has made available a unique quality low-energy negative kaons ??beam??. The SIDDHARTA experiment used this beam to perform unprecedented precision measurements on kaonic atoms, while the AMADEUS experiment plans to perform in the coming years precision measurements on kaon?Cnuclei interactions at low-energies, in particular to study the kaonic nuclei. The two experiments are briefly presented in this paper. 相似文献