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1.
ALEPH Collaboration D. Buskulic D. Casper I. De Bonis D. Decamp P. Ghez C. Goy J. -P. Lees A. Lucotte M. -N. Minard et al. 《Zeitschrift fur Physik C Particles and Fields》1995,69(1):379-392
A data sample of about 3.0 million hadronicZ decays collected by the ALEPH experiment at LEP in the years 1991 through 1994 is used to make an inclusive selection of
B hadron events. In this event sample 4227±140±252B* mesons in the decayB*→Bγ and 1944±108±161B**
u,d
mesons decaying into a B meson and a charged pion are reconstructed. Here and in the followingB**
u,d
denotes the eightL=1(bū) and (bd) states and their charge conjugate.
For the well establishedB* meson the following quantities are obtained:ΔM=M
B*−MB=(45.30±0.35±0.87) MeV/c2 andN
B*/(N
B+N
B*)=(77.1±2.6±7.0)%. The angular distribution of the photons in theB* rest frame is used to measure the relative contribution of longitudinalB* polarization states to beσ
L/(σ
L+σ
T)=(33±6±5)%. 相似文献
2.
High-resolution Fourier transform spectra of CH3OH have been investigated in the infrared region from 930 to 1450 cm−1 in order to map the torsion-rotation energy manifolds associated with the ν7 in-plane CH3 rock, the ν11 out-of-plane CH3 rock, and the ν6 OH bend. Upper-state term values have been determined from the assigned spectral subbands, and have been fitted to power-series expansions to obtain substate origins and effective B-values for the three modes. The substate origins have been grouped into related families according to systematic trends observed in the torsion-vibration energy map, but there are substantial differences from the traditional torsional patterns. There appears to be significant torsion-mediated spectral mixing, and a variety of “forbidden” torsional combination subbands with |Δυt|>1 have been observed, where υt denotes the torsional quantum number (equivalent to υ12). For example, coupling of the (υ6,υt)=(1,0) OH bend to nearby torsionally excited (υ7,υt)=(1,1) CH3-rock and (υ8,υt)=(1,1) CO-stretch states introduces (υ6,υt)=(1,0)←(0,1) subbands into the spectrum and makes the ν7+ν12−ν12 torsional hot band stronger than the ν7 fundamental. The results suggest a picture of strong coupling among the OH-bending, CH3-rocking, and CO-stretching modes that significantly modifies the traditional energy structure and raises interesting and provocative questions about the torsion-vibration identity of a number of the observed states. 相似文献
3.
Despite potential benefits of hair analysis to the equine industry, deposition of drugs in equine hair has been little studied. Trimethoprim/sulphonamides were selected as experimental ‘target’ drugs to investigate factors affecting drug uptake and distribution in equine hair. Hair samples were analysed by HPLC after extraction (0.2 M ammonium hydroxide, 60 °C, 24 h) and SPE (mixed-mode sorbent, C18/SCX). Analytes were resolved on a C18 column (150 × 2.1 mm, 4 μm) by gradient elution (25 mM triethylammonium phosphate, pH 3.0)/acetonitrile), detected at 240/270 nm, and identified by absorption spectra (225–360 nm). Calibration was linear from 0.125–25.0 ng.mg?1. Recoveries were 71–93%. Sulphadimidine, sulphadiazine and trimethoprim were detected in hair from 12 horses. Hair colour and dose size affected the magnitude of drug uptake. Longitudinal distribution profiles of these drugs in tail hair were determined. 相似文献
4.
KL Britton HF Rogers Y Asano T Dairi Y Kato TJ Stillman DW Rice 《Acta crystallographica. Section D, Biological crystallography》1998,53(4):124-126
The novel NAD+-linked opine dehydrogenase from a soil isolate Arthrobacter sp. strain 1C belongs to an enzyme superfamily whose members exhibit quite diverse substrate specificites. Crystals of this opine dehydrogenase, obtained in the presence or absence of co-factor and substrates, have been shown to diffract to beyond 1.8 ? resolution. X-ray precession photographs have established that the crystals belong to space group P21212, with cell parameters a = 104.9, b = 80.0, c = 45.5 ? and a single subunit in the asymmetric unit. The elucidation of the three-dimensional structure of this enzyme will provide a structural framework for this novel class of dehydrogenases to enable a comparison to be made with other enzyme families and also as the basis for mutagenesis experiments directed towards the production of natural and synthetic opine-type compounds containing two chiral centres. 相似文献
5.
J. M. Calvert D. G. Lees D. J. Derry D. Barnes 《Journal of Radioanalytical and Nuclear Chemistry》1972,12(2):271-275
The various nuclear techniques which have been used to study oxygen self-diffusion in oxides are discussed. Results are given
for measurements using resonance capture in the18O(p, α)15N and18O(p, γ)19F reactions and the different techniques are compared. 相似文献
6.
The reactions of lanthanide nitrates, Ln(NO(3))(3), with bis(diphenylphosphino)methane dioxide, Ph(2)P(O)CH(2)P(O)Ph(2) (L), lead to complexes with three distinct classes of structure. At low ratios of Ln:L (<1:1.5) in acetonitrile the ionic complexes [Ln(NO(3))(2)L(2)](+)[Ln(NO(3))(4)L](-) (Ln = Pr, Eu) have been isolated. When carried out with a 1:2 or higher ratio in ethanol the reaction yields Ln(NO(3))(3)L(2) (Ln = La,Ce) and [Ln(NO(3))(2)L(2)H(2)O](+)[NO(3)](-) (Ln = Nd, Gd, Ho). Geometrical isomerism is found for the cations [Ln(NO(3))(2)L(2)H(2)O](+) and is attributed to the extent of hydrogen bonding to the coordinated water. Ligand redistribution occurs on heating in the solid state giving yellow solids in all cases. Crystallization of these materials from ethanol or acetonitrile gives [Ln(NO(3))L(3)](2+).2[NO(3)](-), which have been structurally characterized for Ln = Gd and Yb. Electrospray mass spectra indicate that extensive ligand exchange reactions occur in solution. 相似文献
7.
Wolak MA Thomas CJ Gillespie NB Birge RR Lees WJ 《The Journal of organic chemistry》2003,68(2):319-326
Photochromic fluorinated indolylfulgides have been identified as potential candidates for a wide range of applications including optical switches, photoregulators of biological processes, and optical memory media. In humid environments or biological systems, hydrolytic stability is essential. In an effort to improve hydrolytic stability, a series of indolylfulgimides has been synthesized from a parent trifluoromethyl-substituted indolylfulgide. The nitrogen of the succinimide moiety is linked to either a dimethyl amino or one of seven substituted phenyl groups. The phenyl groups feature substituents with increasing electron-withdrawing ability. The spectral characteristics of each compound have been examined, revealing that the wavelength absorption maxima of each form increases with increasing electron-withdrawing ability of the substituted N-phenyl ring. The quantum yields of the photoreactions have been determined with the N-(phenyl)fulgimide showing a ring closure value of nearly 0.30 in toluene. In addition, the hydrolytic, thermal, and photochemical stabilities of each compound have been measured. The fulgimides exhibit at least a 200-fold enhancement of hydrolytic stability for the Z-form and over a 1000-fold enhancement for the C-form in comparison to the same form of the parent fulgide. The N-(2,3,5,6-tetrafluoro-4-trifluoromethylphenyl)fulgimide can undergo up to 3000 photochemical cycles (coloration followed by bleaching) before losing 20% of its initial absorbance at photostationary state. 相似文献
8.
Tynan E Jensen P Kelly NR Kruger PE Lees AC Moubaraki B Murray KS 《Dalton transactions (Cambridge, England : 2003)》2004,(21):3440-3447
We report herein the single crystal structures of four metal-organic framework complexes incorporating the 4,4'-dicarboxy-2,2'-bipyridine ligand, H(2)dcbp: alpha-[Co(dcbp)(H(2)O)(2)], 1; beta-[Co(dcbp)(H(2)O)(2)], 2, [Ni(dcbp)(H(2)O)(2)], and [[Mn(dcbp)].1/2DEF], 4 (DEF = diethylformamide). In each complex the ligand is deprotonated giving neutral species with 1:1 stoichiometry that form three-dimensional coordination polymers. Supramolecular isomerism (polymorphism) in 1 and 2 arises from the different ligand connectivity around the octahedral Co(II) centres. The two coordinated water molecules in 1 occupy cis positions, which are trans to the chelating bipyridine nitrogen atoms, leaving the carboxylate oxygen atoms in axial trans positions. In 2 all like donors occupy cis positions. Different modes of carboxylate coordination in 1 and 2 give dissimilar network topologies. A rare example of two interpenetrating 6(4)8(2)-b (quartz-like) chiral networks in 1 results from both dcbp carboxylate groups coordinating in a monodentate fashion to adjacent Co(II) centres, whereas in 2 only one carboxylate group bridges between adjacent Co(II) centres giving rise to a single chiral (10,3)-a net. In 1 and 2 the coordinated water molecules hydrogen bond to the non-coordinated carboxylate oxygen atoms. These interactions give rise to water-carboxylate double helices in , and support the coordination network in 2. Strikingly for a pair of dimorphs the crystal densities of 1 and 2 differ by ca. 0.3 g cm(-3)(1.654 vs. 1.940 g cm(-3), respectively). Compound 3 is isomorphous with 1 and likewise features two chiral interpenetrating nets of quartz topology. In 4, chelating bipyridine nitrogen atoms and four carboxylate oxygen atoms from a total of five adjacent dcbp ligands provide distorted octahedral geometry around Mn(II). The carboxylate groups bridge adjacent Mn(II) centres to produce bis-carboxylato chains which cross-link and generate a 3D network that is perforated with channels. The channels are occupied with disordered DEF molecules. The network topology in 4 is quite different to 1-3 and has a (4.6(2))(4(2).6)(4(3).6(6).8(6)) Schlafli notation. Magnetic susceptibility studies performed on 1, 2, [[Mn(dcbp)].1/2DMF] 5 (DMF = dimethylformamide) and [[Mn(dcbp)].2H(2)O] 6 reveal very weak antiferromagnetic coupling between the metal centres in each case. 相似文献
9.
10.
ALEPH Collaboration D. Buskulic I. De Bonis D. Decamp P. Ghez C. Goy J. P. Lees A. Lucotte M. N. Minard P. Odier et al. 《Zeitschrift fur Physik C Particles and Fields》1996,71(3):357-378
The electroweak mixing angle is determined with high precision from measurements of the mean difference between forward and
backward hemisphere charges in hadronic decays of the Z. A data sample of 2.5 million hadronic Z decays recorded over the
period 1990 to 1994 in the ALEPH detector at LEP is used. The mean charge separation between event hemispheres containing
the original quark and antiquark is measured for
and
events in subsamples selected by their long lifetimes or using fastD*’s. The corresponding average charge separation for light quarks is measured in an inclusive sample from the anticorrelation
between charges of opposite hemispheres and agrees with predictions of hadronisation models with a precision of 2%. It is
shown that differences between light quark charge separations and the measured average can be determined using hadronisation
models, with systematic uncertainties constrained by measurements of inclusive production of kaons, protons andΛ’s. The separations are used to measure the electroweak mixing angle precisely as sin2
ϑ
w
eff
=0.2322±0.0008(exp.stat.) ±0.0007(exp.syst.)±0.0008(sep.). The first two errors are due to purely experimental sources whereas
the third stems from uncertainties in the quark charge separations.
Supported by Dirección General de Investigación Científica y Técnica, Spain 相似文献