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131.
Resistivity and thermal conductivity of the intermediate valence compound CePd3 between 1.3 and 300 K are compared with those of the nonmagnetic and magnetic reference compounds YPd3 and GdPd3 and of alloys of the type Ce1–xRE
x
Pd3 with RE=Y, Gd and 0.01<x<0.5. The analysis reveals the existence of a maximum metallic resistivity of 300 cm for CePd3. The intrinsic resistivity of CePd3 rises proportional toT
2 up to 100 K, with a coefficientB about 107 times larger than e.g. in copper. We interpret this with indirect electron-electron scattering mediated through valence transitions. 相似文献
132.
Schneider JJ Spickermann D Labahn T Magull J Fontani M Laschi F Zanello P 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(20):3686-3691
Reaction of the half-sandwich complexes [(eta5-Me4RC5)M(eta2:O-acac)] (M = Co, Ni; R = Me or Et) with di- and trianions of the polycondensed pi-hydrocarbon decacyclene results in formation of the first Co and Ni triple-decker complexes of this hydrocarbon. For the title compound NMR spectra as well as a crystal structure analysis reveal an antarafacial coordination of two (eta5-Me4EtC5)Co fragments at the central six-membered ring and one of the neighboring five-membered rings of decacyclene. The bridging pi-perimeter decacyclene displays a bowl-shaped topology. In the case of Ni, coordination of two (eta5-Me5C5)Ni fragments at the central six-membered ring of decacyclene is observed, based on the results of 1H and 13C NMR studies. This coordination mode is without precedent for nickel organometallic compounds reported so far. The cobalt complex shows a rich spectroelectrochemistry. Results of cyclic voltammetry and coupled ESR experiments reveal a strong interaction of both metal centers in the mixed-valent monocation of [(eta5-Me4EtC5)Co2(mu-eta5:eta4-C36H18)]. This categorizes the title compound into Robin Day class III. 相似文献
133.
It is shown that insertion in methacrylic polymers of bulky electron donor/acceptor side-groups with taper-shaped flourinated tails promotes a self-organization of the respective side-chain polymers due to the space demands of the bulky D/A side-groups, leading to a columnar hexagonal mesophase. The presence of an Lc-phase is evidenced by DSC and identified by X-ray analysis. The orientation in the respective copolymers and polymer blends is additionally improved by the CT-interaction between the D/A side-groups. An increased packing effect due to this CT-orientation effect is evidenced in DSC by an increase of the respective transition temperatures. CT-interaction is responsible as well for a preferential polymerization of monomeric D/A-complexes leading to copolymers of alternating structures and for a zip-like arrangement along the main chain of the A/D-complexes between the interacting side-groups in polymer blends. Formation of mesophases is even observed in CT-interacting blends between the Lc-D/A side-chain polymethacrylates and the respective amorphous D/A side-chain polysiloxanes.This revised version was published online in November 2005 with corrections to the Cover Date. 相似文献
134.
E. E. B. Campbell R. R. Schneider A. Hielscher A. Tittes R. Ehlich I. V. Hertel 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1992,22(2):521-527
The collisional velocity dependence of the cross sections for fragmentation of mass-selected (CO2) n + (n+2...7) clusters in collisions with Ar atoms is presented. Interesting structure can be observed in the cross sections which indicate that the collision occurs between the Ar atom and one CO2 molecule within the cluster. The results may be explained by assuming that the collision leads to either vibrational excitation of a loosely bound CO2 monomer which then leaves the cluster or excitation of the entire cluster to a dissociative state. 相似文献
135.
Sellmann D Hille A Rösler A Heinemann FW Moll M Brehm G Schneider S Reiher M Hess BA Bauer W 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(4):819-830
In the quest for low-molecular-weight metal sulfur complexes that bind nitrogenase-relevant small molecules and can serve as model complexes for nitrogenase, compounds with the [Ru(PiPr(3))('N(2)Me(2)S(2)')] fragment were found ('N(2)Me(2)S(2)'(2-)=1,2-ethanediamine-N,N'-dimethyl-N,N'-bis(2-benzenethiolate)(2-)). This fragment enabled the synthesis of a first series of chiral metal sulfur complexes, [Ru(L)(PiPr(3))('N(2)Me(2)S(2)')] with L=N(2), N(2)H(2), N(2)H(4), and NH(3), that meet the biological constraint of forming under mild conditions. The reaction of [Ru(NCCH(3))(PiPr(3))('N(2)Me(2)S(2)')] (1) with NH(3) gave the ammonia complex [Ru(NH(3))(PiPr(3))('N(2)Me(2)S(2)')] (4), which readily exchanged NH(3) for N(2) to yield the mononuclear dinitrogen complex [Ru(N(2))(PiPr(3))('N(2)Me(2)S(2)')] (2) in almost quantitative yield. Complex 2, obtained by this new efficient synthesis, was the starting material for the synthesis of dinuclear (R,R)- and (S,S)-[micro-N(2)[Ru(PiPr(3))('N(2)Me(2)S(2)')](2)] ((R,R)-/(S,S)-3). (Both 2 and 3 have been reported previously.) The as-yet inexplicable behavior of complex 3 to form also the R,S isomer in solution has been revealed by DFT calculations and (2)D NMR spectroscopy studies. The reaction of 1 or 2 with anhydrous hydrazine yielded the hydrazine complex [Ru(N(2)H(4))(PiPr(3))('N(2)Me(2)S(2)')] (6), which is a highly reactive intermediate. Disproportionation of 6 resulted in the formation of mononuclear diazene complexes, the ammonia complex 4, and finally the dinuclear diazene complex [micro-N(2)H(2)[Ru(PiPr(3))('N(2)Me(2)S(2)')](2)] (5). Dinuclear complex 5 could also be obtained directly in an independent synthesis from 1 and N(2)H(2), which was generated in situ by acidolysis of K(2)N(2)(CO(2))(2). Treatment of 6 with CH(2)Cl(2), however, formed a chloromethylated diazene species [[Ru(PiPr(3))('N(2)Me(2)S(2)')]-micro-N(2)H(2)[Ru(Cl)('N(2)Me(2)S(2)CH(2)Cl')]] (9) ('N(2)Me(2)S(2)CH(2)Cl'(2-) =1,2-ethanediamine-N,N'-dimethyl-N-(2-benzenethiolate)(1-)-N'-(2-benzenechloromethylthioether)(1-)]. The molecular structures of 4, 5, and 9 were determined by X-ray crystal structure analysis, and the labile N(2)H(4) complex 6 was characterized by NMR spectroscopy. 相似文献
136.
Peter Resch F. W. Schneider Richard J. Field Mária Burger 《Reaction Kinetics and Catalysis Letters》1990,42(2):189-200
A mechanism is discussed which reproduces in simulations the oscillations during the methylene-blue catalyzed reduction of O2 by HS– in a continuous-flow, strirred tank reactor (CSTR). It contains 14 reactions and is based on experiments and simulations of simpler reactions including the reduction of MB+ by HS– in the absence and presence of O2 and the reactions of H2O2 and O2 with HS–. All experiments on component reactions as well as the CSTR oscillations can be simulated by the same set of reactions and rate constants. The major dynamic feature of the mechanism is the competition for MB. by the oxidizing agents O2 and H2O2 and the reducing agents HS– and HS.. The species MB. is the radical intermediate between the colored (MB+) and colorless (MBH) forms of methylene blue. 相似文献
137.
The111Cd quadrupole coupling in the spinel CdCr2Se4 is investigated by TDPAC after different sample treatments. The experiments are consistent with Se vacancies causing the non-cubic probe environments and with the assumption that the majority of the111In atoms are positioned at A-sites. 相似文献
138.
S. Schneider F. Simon D. Pleul H.-J. Jacobasch 《Analytical and bioanalytical chemistry》1997,358(1-2):244-247
Flow sorption calorimetry (FSC) can be a useful tool to estimate the Lewis acid-base behaviour of the surface of organic
polymers with less than 1 m2/g surface area. Polyethylene powders grafted with different amounts of acrylic acid have been chosen as samples. The surface
of the powders was investigated by means of X-ray photoelectron spectroscopy (XPS) at first and than brought into contact
with the strong electron donor triethylamine in a special FSC measuring system. The heat of the displacement isotherm together
with the surface excess isotherm of triethylamine adsorbed onto the powders was determined. The results obtained with FSC
and XPS were well correlated and gave a comprehensive picture of the acidic surface character of modified polyethylene.
Received: 19 September 1996 / Revised: 22 January 1997 / Accepted: 26 January 1997 相似文献
139.
Volker Böhmer Friedhelm Schneider Keiichi Fukuyama Shigeo Fujii 《Monatshefte für Chemie / Chemical Monthly》1985,116(12):1419-1432
Cyclic esters of adipic acid, suberic acid and sebacic acid were prepared by reaction of the acid dichlorides and pyrocatechol or hydroquinone in benzene under high dilution conditions. While only the cyclic dimers could be obtained from hydroquinone, pyrocatechol formed cyclic monomers as well as cyclic dimers (and also a cyclic dimer with succinic acid). The structure of all compounds was confirmed by1H-NMR- and mass spectra. The crystal structures of the pyrocatechol esters were determined by single crystal X-ray analysis.
Cyclische Ester aliphatischer Dicarbonsäuren mit Brenzcatechin und Hydrochinon
Zusammenfassung Es wurden cyclische Ester von Adipinsäure, Korksäure und Sebacinsäure durch Reaktion der entsprechenden Säure-Dichloride mit Brenzcatechin oder Hydrochinon bei hoher Verdünnung hergestellt. Während mit Hydrochinon lediglich die cyclischen Dimeren erhalten werden konnten, wurden mit Brenzcatechin sowohl cyclische Monomere als auch cyclische Dimere erhalten (ebenfalls das cyclische Dimer mit Bernsteinsäure). Die Strukturen wurden mittels1H-NMR und Massenspektren gesichert. Die Kristallstrukturen der Brenzcatechin-Ester wurden mittels Röntgenstrukturanalyse bestimmt.相似文献
140.
Chromatographia - Three groups of metabolites were analyzed in extracts of rat hepatocytes by an HPLC method: (i) nucleotides (ATP, ADP, AMP, GTP, GDP, UTP, UDP, IMP, UMP), (ii) nucleosides and... 相似文献