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1.
2.
F. Seiffert R. Schwengner G. Winter L. Funke W. Lieberz R. Reinhardt K. P. Schmittgen D. Weil R. Wrzal K. O. Zell P. von Brentano 《Zeitschrift für Physik A Hadrons and Nuclei》1991,340(2):141-153
Excited states of73Se have been investigated up to spin, 21/2 using techniques of in-beamγ-ray spectroscopy in connection with the70Ge(α, n) reaction. Mean lifetimes of 12 levels have been determined applying Doppler-shift andγ-RF-methods. Five different bands have been identified that reflect a variety of different excitation modes. The decoupled 9/2+ band is likely to correspond to an oblate deformation while the 5/2+ band is interpreted as a strongly coupled prolate band built on the Nilsson configuration [422] 5/2+. The 3/2? band is a strongly coupled band built on the [301] 3/2} configuration.Nuclear reactions:70Ge(α,n),E=14, 16, 18, 19, 20MeV; measuredE γ,I γ,σ(E γ,θ),γγ-coin, linear polarization, DSA,γ(t).75Se deduced levels,I, π, τ, δ(E2/M1), B(σλ). Enriched targets, Ge detectors. 相似文献
3.
Friedrich Weil 《Fresenius' Journal of Analytical Chemistry》1872,11(1):284
Ohne Zusammenfassung 相似文献
4.
Baran EJ Weil M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,61(4):707-710
The infrared and Raman spectra of the crystalline hexaoxotellurates Hg3TeO6 and Hg2TeO5 were recorded and discussed on the basis of a site symmetry analysis derived from known structural data. Approximate values for the Te-O bond force constants are reported and some comparisons with related species are made. 相似文献
5.
Weil Joseph Brewer Mark Hendrickson Richard Sarikaya Ayda Ladisch Michael R. 《Applied biochemistry and biotechnology》1998,(1):99-111
Yellow poplar wood sawdust consists of 41% cellulose and 19% hemicellulose. The goal of pressure cooking this material in
water is to hydrate the more chemically resistive regions of cellulose in order to enhance enzymatic conversion to glucose.
Pretreatment can generate organic acids through acid-catalyzed degradation of monosaccharides formed because of acids released
from the biomass material or the inherent acidity of the water at temperatures above 160°C. The resulting acids will further
promote the acid-catalyzed degradation of monomers that cause both a reduction in the yield and the formation of fermentation
inhibitors such as hydroxymethyl furfural and furfural. A continuous pH-monitoring system was developed to help characterize
the trends in pH during pretreatment and to assist in the development of a base (2.0 M KOH) addition profile to help keep
the pH within a specified range in order to reduce any catalytic degradation and the formation of any monosac-charide degradation
products during pretreatment. The results of this work are discussed. 相似文献
6.
Richard Ley D. Hagena D. Weil G. Werth W. Arnold H. Schneider 《Hyperfine Interactions》1994,89(1):327-341
Electric dipole transitions in the microwave range have been induced between the fine-structure levels of positronium in the excited staten=2. As an indication of the transitions, we used the increase in Lyman- radiation when the metastable 23S1-level is depopulated. The results for the transitions 23S123P0,1,2 are
0=18499.65±1.20±4.00 MHz,
1=13012.42 ±0.65±1.54 MHz and
2=8624.38±0.54±1.40 MHz. The first error is statistical and the second systematic. The precision of the present measurement has improved by a factor of 3, compared to previous data. Recent bound state QED-calculations have been extended to the orderR
t8
4ln
–1. The not yet completely calculated orderR
t8
4 is estimated to contribute less than 1 MHz. Our experimental results are in good agreement with theory. By applying a weak magnetic field, we were able to observe the transition 23S121P1 which is strictly forbidden byC-invariance in zero field. Our result, corrected for Zeeman- and motional Starkeffect, is
3=11180.0±5.0±4.0 MHz. An upper limit for theC-violating matrix element of
MHz could be deduced. Our experiment used moderated slow positrons from the bremsstrahlung and pair production of a pulsed electron linear accelerator (TEPOS facility at the university of Giessen). 相似文献
7.
Two pyrene-labeled hydroxylamines, 5-Bn and 5-Bz, O-protected with the benzyl and the benzoyl group, respectively, have been prepared for the generation of siderophore-based new chelators incorporating both the pyrene chromophore and the hydroxamic acid functionality. 5-Bz formed the starting point toward the synthesis of the tripod-shaped trishydroxamate, 1. That trichromophoric ligand displays remarkable fluorescence emission properties (dual emission: "monomer" and excimer type) which are markedly and selectively modified by binding Fe(NO(3))(3) and Ga(NO(3))(3). Ferric ions induce a quasi total quenching of the pyrene fluorescence, whereas the nonquenching Ga(III) cations are observed to affect the value of the excimer-to-monomer fluorescence intensity ratio. Ethylenediaminetetraacetic acid (EDTA) competition reactions yielded an estimated value of 3.8 for log K of the complex LFe in methanol/water (80/20 v/v), where K = ([LFe][H(+)](3))/([LH(3)][Fe(3+)]) and L is the ligand in its totally deprotonated form. Compound 1 is the prototype of a new class of photoresponsive molecular systems which could act as sensitive probes for metal cation detection and recognition. 相似文献
8.
Matthias Weil 《无机化学与普通化学杂志》2004,630(7):1048-1053
Single crystals of HgII(H4TeVIO6) (colourless to light‐yellow, rectangular plates) and HgI2(H4TeVIO6)(H6TeVIO6)·2H2O (colourless, irregular) were grown from concentrated solutions of orthotelluric acid, H6TeO6, and respective solutions of Hg(NO3)2 and Hg2(NO3)2. The crystal structures were solved and refined from single crystal diffractometer data sets (HgII(H4TeVIO6): space group Pna21, Z = 4, a =10.5491(17), b = 6.0706(9), c = 8.0654(13)Å, 1430 structure factors, 87 parameters, R[F2 > 2σ(F2)] = 0.0180; HgI2(H4TeVIO6)(H6TeVIO6)·2H2O: space group P1¯, Z = 1, a = 5.7522(6), b = 6.8941(10), c = 8.5785(10)Å, α = 90.394(8), β = 103.532(11), γ = 93.289(8)°, 2875 structure factors, 108 parameters, R[F2 > 2σ(F2)] = 0.0184). The structure of HgII(H4TeVIO6) is composed of ribbons parallel to the b axis which are built of [H4TeO6]2— anions and Hg2+ cations held together by two short Hg—O bonds with a mean distance of 2.037Å. Interpolyhedral hydrogen bonding between neighbouring [H4TeO6]2— groups, as well as longer Hg—O bonds between Hg atoms of one ribbon to O atoms of adjacent ribbons lead, to an additional stabilization of the framework structure. HgI2(H4TeVIO6)(H6TeVIO6)·2H2O is characterized by a distorted hexagonal array made up of [H4TeO6]2— and [H6TeO6] octahedra which spread parallel to the bc plane. Interpolyhedral hydrogen bonding between both building units stabilizes this arrangement. Adjacent planes are stacked along the a axis and are connected by Hg22+ dumbbells (d(Hg—Hg) = 2.5043(4)Å) situated in‐between the planes. Additional stabilization of the three‐dimensional network is provided by extensive hydrogen bonding between interstitial water molecules and O and OH‐groups of the [H4TeO6]2— and [H6TeO6] octahedra. Upon heating HgI2(H4TeVIO6)(H6TeVIO6)·2H2O decomposes into TeO2 under formation of the intermediate phases HgII3TeVIO6 and the mixed‐valent HgIITeIV/VI2O6. 相似文献
9.
Wolfgang Weil 《manuscripta mathematica》1981,36(1):1-18
It is shown that there exists a distribution T on n ( unit sphere of Euclidean n-space) such that the mixed volume V(K1,...,Kn) equals
for all convex bodies Ki, where
is the support function of ki and denotes the tensor product. As a consequence, mixed volumes are approximated uniformly by n-fold integrals of the corresponding support functions. 相似文献
10.
Matthias Weil 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(3):i37-i39
The crystal structure of Hg3AlF6O2H, trimercury(II) aluminium hydrogen hexafluoride dioxide, can be derived from a slightly distorted cubic close‐packed (ccp) arrangement of the metal atoms, where three quarters of the positions are occupied by Hg atoms and one quarter by Al atoms. The F and O atoms are considerably dislocated from the tetrahedral voids of this arrangement, thus forming [HgO2F6] polyhedra, with two short Hg—O distances, two intermediate Hg—F distances and four longer Hg—F distances, and nearly ideal [AlF6] octahedra. The H atoms are presumably located close to the inversion centre. Their positions were derived from crystal chemical arguments, and they take part in the formation of O—H?O hydrogen bonds between two O atoms, with an O?O distance of 2.562 (9) Å. 相似文献