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91.
Gunter Heymann Jan F. Riecken Sudhindra Rayaprol Sandra Christian Rainer Pöttgen Prof. Dr. Hubert Huppertz PD Dr. 《无机化学与普通化学杂志》2007,633(1):77-82
The high‐pressure (HP) modification of CePdSn was synthesized under multianvil high‐pressure (10.5 GPa) high‐temperature (1100 °C) conditions from the normal‐pressure (NP) modification. The structures of both modifications were studied by X‐ray powder and single crystal diffraction: TiNiSi type, Pnma, a = 754.1(2), b = 470.6(1), c = 798.4(3) pm, wR2 = 0.0333, 945 F2 values, 20 variables for NP‐CePdSn and ZrNiAl type, , a = 760.03(5), c = 416.06(3) pm, wR2 = 0.0443, 248 F2 values, 13 variables for HP‐CePdSn. The structural chemistry of both modifications is goverened by platinum centered trigonal prisms. The platinum and tin atoms in NP‐CePdSn and HP‐CePdSn build up a three‐dimensional [PdSn] network in which the cerium atoms fill channels. Susceptibility measurements on HP‐CePdSn reveal an experimental magnetic moment of 2.55(1) μB/Ce atom in the paramagnetic region. At 5 K a paramagnetic‐to‐antiferromagnetic transition is evident from magnetization and specific heat measurements. 相似文献
92.
Matthias Weil PD Dr. 《无机化学与普通化学杂志》2007,633(8):1217-1222
Single crystals of a third modification of Ag2Te2O6 (denoted as Ag2Te2O6–III) and of Ag4TeO5 have been obtained as minor by‐products during hydrothermal phase formation experiments in the system Ag‐Hg‐Te‐O. The crystal structure of Ag2Te2O6–III (P21/c, Z = 4, a = 6.4255(10), b = 6.9852(11), c = 13.204(2) Å, β = 90.090(3)°, 1885 independent reflections, R[F2 > 2σ(F2)] = 0.0334, wR2(F2 all) = 0.0817) comprises tellurium in oxidation states +IV and +VI and is topologically related to the structure of the Ag2Te2O6–I modification, which consists of similar layers and interjacent layers of Ag+ cations. Ag4TeO5 (C2/c, Z = 8, a = 16.271(2), b = 6.0874(10), c = 11.4373(16) Å, β = 106.730(10)°, 2372 independent reflections, R[F2 > 2σ(F2)] = 0.0288, wR2(F2 all) = 0.0737) is made up of a layer‐like arrangement of isolated [TeVI2O10] double octahedra and of Ag+ cations situated both in layers parallel and inside the layers of the anionic moieties. 相似文献
93.
Two-dimensional electrophoresis of membrane proteins 总被引:1,自引:0,他引:1
One third of all genes of various organisms encode membrane proteins, emphasizing their crucial cellular role. However, due
to their high hydrophobicity, membrane proteins demonstrate low solubility and a high tendency for aggregation. Indeed, conventional
two-dimensional gel electrophoresis (2-DE), a powerful electrophoretic method for the separation of complex protein samples
that applies isoelectric focusing (IEF) in the first dimension and sodium dodecyl sulfate polyacrylamide gel electrophoresis
(SDS-PAGE) in the second dimension, has a strong bias against membrane proteins. This review describes two-dimensional electrophoretic
techniques that can be used to separate membrane proteins. Alternative methods for performing conventional 2-DE are highlighted;
these involve replacing the IEF with electrophoresis using cationic detergents, namely 16-benzyldimethyl-n-hexadecylammonium chloride (16-BAC) and cetyl trimethyl ammonium bromide (CTAB), or the anionic detergent SDS. Finally, the
separation of native membrane protein complexes through the application of blue and clear native gel electrophoresis (BN/CN-PAGE)
is reviewed, as well as the free-flow electrophoresis (FFE) of membranes. 相似文献
94.
Lankshear MD Evans NH Bayly SR Beer PD 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(14):3861-3870
We present the rational design and anion-binding properties of the first anion-templated pseudorotaxanes and catenanes in which the "wheel" component is provided by a calix[4]arene macrobicyclic unit. The designs and syntheses of two new calix[4]arene macrobicycles, 2 and 3, are presented, and the abilities of these new species both to bind anions and to undergo anion-dependent pseudorotaxane formation are demonstrated. Furthermore, it is shown that performing ring-closing metathesis reactions on some of these pseudorotaxane assemblies gives novel catenane species 14 and 15, in which the yield of interlocked molecule obtained is critically dependent on the presence of a suitable anion template, namely, chloride. Exchange of the chloride anion in catenane 14 a for hexafluorophosphate gives catenane 14 d, which contains a unique anion-binding domain defined by the permanently interlocked hydrogen-bond-donating calix[4]arene macrobicycle and pyridinium macrocycle fragments. The anion-binding properties of this domain are presented, and shown to differ from non-interlocked components. 相似文献
95.
T.M. Huber A. Adamczak J.M. Bailey G.A. Beer J.L. Beveridge B.P. Ellerbusch M.C. Fujiwara R. Jacot-Guillarmod P. Kammel S.K. Kim P.E. Knowles A.R. Kunselman G.J. Lindquist M. Maier V.E. Markushin G.M. Marshall C.J. Martoff G.R. Mason F. Mulhauser A. Olin C. Petitjean T.A. Porcelli J. Woźniak J. Zmeskal 《Hyperfine Interactions》1999,118(1-4):159-161
In recent TRIUMF experiments, a μ- beam is stopped in a solid hydrogen film with a small fraction of T2. The Ramsauer-Townsend (RT) mechanism allows μt to escape into vacuum with a few eV of energy. To study the emission process, an imaging system was used to determine the
position of muon decays. Experimental histograms are in good agreement with a Monte Carlo simulation.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
96.
G.M. Marshall T.A. Porcelli A. Adamczak J.M. Bailey G.A. Beer M.P. Faifman M.C. Fujiwara T.M. Huber R. Jacot-Guillarmod P. Kammel S.K. Kim P.E. Knowles A.R. Kunselman M. Maier V.E. Markushin G.R. Mason F. Mulhauser A. Olin C. Petitjean J. Zmeskal 《Hyperfine Interactions》1999,118(1-4):89-101
Solid hydrogen in the form of an inhomogeneous layered target offers several experimental advantages when compared with liquid
or gas. Beams of non-thermalized muonic hydrogen atoms allow us to explore resonant molecular ion formation processes near
eV kinetic energies. Isotopically specific layers make it possible to separate competing and confusing interactions and to
employ the time of flight for comparison with predictions based on theoretical energy dependences. Unambiguous charged fusion
product detection simplifies absolute intensity measurements.
The systematic uncertainties encountered in resonant molecular ion formation measurements, using solid hydrogen target layers,
are being investigated with simulations which use the many calculated energy-dependent rates and cross-sections which are
now available. The importance of the rates for processes such as muon transfer and elastic scattering are discussed, and results
of some recent analyses are presented.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
97.
AymanA. Abdel‐Shafi PaulD. Beer RogerJ. Mortimer Francis Wilkinson 《Helvetica chimica acta》2001,84(9):2784-2795
Photophysical properties in dilute MeCN solution are reported for seven RuII complexes containing two 2,2′‐bipyridine (bpy) ligands and different third ligands, six of which contain a variety of 4,4′‐carboxamide‐disubstituted 2,2′‐bipyridines, for one complex containing no 2,2′‐bipyridine, but 2 of these different ligands, for three multinuclear RuII complexes containing 2 or 4 [Ru(bpy)2] moieties and also coordinated via 4,4′‐carboxamide‐disubstituted 2,2′‐bipyridine ligands, and for the complex [(Ru(bpy)2(L)]2+ where L is N,N′‐([2,2′‐bipyridine]‐4,4′‐diyl)bis[3‐methoxypropanamide]. Absorption maxima are red‐shifted with respect to [Ru(bpy)3]2+, as are phosphorescence maxima which vary from 622 to 656 nm. The lifetimes of the lowest excited triplet metal‐to‐ligand charge transfer states 3MLCT in de‐aerated MeCN are equal to or longer than for [Ru(bpy)3]2+ and vary considerably, i.e., from 0.86 to 1.71 μs. Rate constants kq for quenching by O2 of the 3MLCT states were measured and found to be well below diffusion‐controlled, ranging from 1.2 to 2.0⋅109 dm3 mol−1 s−1. The efficiencies f of singlet‐oxygen formation during oxygen quenching of these 3MLCT states are relatively high, namely 0.53 – 0.89. The product of kq and f gives the net rate constant k for quenching due to energy transfer to produce singlet oxygen, and kq−k equals k, the net rate constant for quenching due to energy dissipation of the excited 3MLCT states without energy transfer. The quenching rate constants were both found to correlate with ΔGCT, the free‐energy change for charge transfer from the excited Ru complex to oxygen, and the relative and absolute values of these rate constants are discussed. 相似文献
98.
99.
100.
Andrew J. Taylor Dr. Robert Hein Sophie C. Patrick Prof. Jason J. Davis Prof. Paul D. Beer 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2024,136(6):e202315959
Anion sensing via either optical or electrochemical readouts has separately received enormous attention, however, a judicious combination of the advantages of both modalities remains unexplored. Toward this goal, we herein disclose a series of novel, redox-active, fluorescent, halogen bonding (XB) and hydrogen bonding (HB) BODIPY-based anion sensors, wherein the introduction of a ferrocene motif induces remarkable changes in the fluorescence response. Extensive fluorescence anion titration, lifetime and electrochemical studies reveal anion binding-induced emission modulation through intramolecular photoinduced electron transfer (PET), the magnitude of which is dependent on the nature of both the XB/HB donor and anion. Impressively, the XB sensor outperformed its HB congener in terms of anion binding strength and fluorescence switching magnitude, displaying significant fluorescence turn-OFF upon anion binding. In contrast, redox-inactive control receptors display a turn-ON response, highlighting the pronounced impact of the introduction of the redox-active ferrocene on the optical sensing performance. Additionally, the redox-active ferrocene motif also serves as an electrochemical reporter group, enabling voltammetric anion sensing in competitive solvents. The combined advantages of both sensing modalities were further exploited in a novel, proof-of-principle, fluorescence spectroelectrochemical anion sensing approach, enabling simultaneous and sensitive read out of optical and electrochemical responses in multiple oxidation states and at very low receptor concentration. 相似文献