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排序方式: 共有1613条查询结果,搜索用时 31 毫秒
11.
Ursula E. Spichiger Rudolf Eugster E. Haase G. Rumpf Peter Gehrig Angela Schmid Bruno Rusterholz Wilhelm Simon 《Fresenius' Journal of Analytical Chemistry》1991,341(12):727-731
Summary The selectivity of a new magnesium ionophore (ETH 7025) induced in membranes of different compositions is experimentally studied in view of the ion activities in human serum. The required selectivity coefficient against calcium for the application of an ion-selective magnesium electrode to human serum is calculated for the worst case. Other critical parameters for the application of a liquid PVC-based ion-selective membrane to undiluted human serum discussed are: the sensor lifetime which is related to the lipophilicity of the carrier as well as the ruggedness of the membrane against interactions with components of the relatively lipophilic sample. 相似文献
12.
Ursula Ehrmann Lante Carbognani Claudio Ceccarelli 《Journal of separation science》1992,15(7):467-471
Two methods have been developed for the determination of trace levels of acetonitrile and propionitrile in light naphthas. One involves clean-up and preconcentration by medium pressure liquid chromatography (MPLC) in which nitriles are concentrated ten-fold while the complex hydrocarbon matris is removed. The concentrated solution is then analyzed by high resolution GC with flame ionization detection. The second method involves direct injection of samples into a capillary GC equipped with chemiluminescence nitrogen detection. The results and repeatability obtained from both methods are comparable. Preconcentration enables identification by GC-MS and simultaneous analysis of other polar species, with no need for selective detectors. Direct analysis is, on the other hand, much less time-consuming and requires less sample. 相似文献
13.
Enhancing the enzymatic hydrolysis of cellulosic materials using simultaneous ball milling 总被引:1,自引:0,他引:1
Mais Ursula Esteghlalian Ali R. Saddler John N. Mansfield Shawn D. 《Applied biochemistry and biotechnology》2002,98(1-9):815-832
One of the limiting factors restricting the effective and efficient bioconversion of softwood-derived lignocellulosic residues
is the recalcitrance of the substrate following pretreatment. Consequently, the ensuing enzymatic process requires relatively
high enzyme loadings to produce monomeric carbohydrates that are readily fermentable by ethanologenic microorganisms. In an
attempt to circumvent the need for larger enzyme loadings, a simultaneous physical and enzymatic hydrolysis treatment was
evaluated. A ball-mill reactor was used as the digestion vessel, and the extent and rate of hydrolysis were monitored. Concurrently,
enzyme adsorption profiles and the rate of conversion during the course of hydrolysis were monitored. α-Cellulose, employed
as a model substrate, and SO2-impregnated steam-exploded Douglas-fir wood chips were assessed as the cellulosic substrates. The softwood-derived substrate
was further posttreated with water and hot alkaline hydrogen peroxide to remove >90% of the original lignin. Experiments at
different reaction conditions were evaluated, including substrate concentration, enzyme loading, reaction volumes, and number
of ball beads employed during mechanical milling. It was apparent that the best conditions for the enzymatic hydrolysis of
α-cellulose were attained using a higher number of beads, while the presence of air-liquid interface did not seem to affect
the rate of saccharification. Similarly, when employing the lignocellulosic substrate, up to 100% hydrolysis could be achieved
with a minimum enzyme loading (10 filter paper units/g of cellulose), at lower substrate concentrations and with a greater
number of reaction beads during milling. It was apparent that the combined strategy of simultaneous ball milling and enzymatic
hydrolysis could improve the rate of saccharification and/or reduce the enzyme loading required to attain total hydrolysis
of the carbohydrate moieties. 相似文献
14.
4-(N,N-dioctylamino)-4-trifluoroacetyl-azobenzene (ETHT 4001), together with the catalyst tridodecylmethylammonium chloride, is dissolved in the hydrophilic polymer polyurethane Tecoflex. The resulting membrane layers show high sensitivity toward water vapour and allow the application of the membranes for humidity measurements. Upon exposure to humid air, the membrane exhibits a decrease in absorbance at a wavelength around 490 nm and an increase at around 430 nm. This signal change is caused by the conversion of the trifluoroacetyl group of the reactand into a diol, thus changing the electron delocalisation of the reactand. The sensor layer exhibits a dynamic range from 1% to 100% RH with highest sensitivity in the 5%–40% RH range. The limit of detection is 0.5% RH. The amount of added catalyst enables the sensitive range to be tailored. The selectivity over ethanol and carbonate is sufficient for the membrane to be used for long-term measurements of air. The change in colour of the humidity-sensitive membrane from red to yellow also means it can be used as an optical test strip. 相似文献
15.
J. Kötzler D. Görlitz R. Dombrowski M. Pieper 《Zeitschrift für Physik B Condensed Matter》1994,94(1-2):9-12
At internal magnetic fields much smaller than the spontaneous magnetizationM
s
(T) but large compared to the weak anisotropy field,H
A
20 Oe, the internal susceptibility measured parallel toM by NMR and low frequency ac-susceptibility is observed to diverge asH
–1/2 for temperatures up to 0.998T
c
. Numerous theoretical work predicted suchH
–1/2-singularity to arise from massless Goldstone-modes associated with the perpendicular susceptibility of a Heisenberg system. The temperature variation of the amplitude,
z
·H
–1/2, agrees with the results of the spin-wave and more general hydrodynamic theories, while the magnitude reveals the suppression of one Goldstone polarization by the dipoledipole interaction. In contrast to a previous renormalization-group estimate, a crossover to thermal critical behavior nearT
c
is not observed. 相似文献
16.
Different methods for representing the upper orbitals in Rydberg transitions are tested by means of a series of ab initio SCF and CI calculations for ethylene and various properties for such diffuse united-atom species are reported. Calculated transition energies indicates the maximum separation between individual components of the (π,3d) Rydberg species to be in the 0.1-0.2 range, with similarly small energy separations being obtained for the corresponding (π, 3p) states 相似文献
17.
18.
Biesemans M Martins JC Jurkschat K Pieper N Seemeyer S Willem R 《Magnetic resonance in chemistry : MRC》2004,42(9):776-780
It is demonstrated that long-range nJ(1H,117Sn) coupling constants down to 0.3 Hz, can be accurately quantified from non-linear fitting of the sine modulation of the associated 1H-117Sn correlation cross-peak intensities sampled as a function of the heteronuclear antiphase coherence preparation time in the 1H-117Sn J-HMQC pulse sequence. The contribution of additional, undesired modulations is illustrated and assessed using the product operator formalism, and is traced back to contributions that arise from miss-setting of the wandering 180 degrees pulse angle in the constant time period. The power of the method and its use in the characterization of weak intramolecular donor-acceptor interactions are illustrated by the determination of long-range nJ(1H,117Sn) coupling constants of bis[3-(dimethylamino)propyl]tin derivatives, [Me2N(CH2)3]2SnR2 (', R = Me; 3, R = Ph; 4, R = t-Bu). By comparing these with the values found for the corresponding bis(4-methylpentyl)tin derivatives, [Me2CH(CH2)3]2SnR2 (2', R = Me; 3', R = Ph), which lack such interactions, the use of long-range coupling constants to detect intramolecular donor-acceptor interactions is evaluated. It is concluded that nJ(1H,117Sn) couplings up to six bonds through an organic carbon chain can be quantified, whether donor-acceptor interactions are present or not. Furthermore, evidence is presented that, when two scalar coupling pathways co-exist, the pathway involving an intramolecular donor-acceptor interaction can have opposite sign, thus decreasing the overall coupling constant to a value smaller than that actually measured in the absence of a donor-acceptor interaction, where only one coupling pathway is active. There is nevertheless clear numerical value discrimination in the series of compounds investigated between long-range couplings in derivatives without weak intramolecular donor-acceptor interactions and those where such interactions can exist. 相似文献
19.
Ursula Baumann 《Fresenius' Journal of Analytical Chemistry》1963,193(6):456
Ohne Zusammenfassung
Folin, O.: Hoppe-Seylers Z. physiol. Chem. 41, 223 (1904); vgl. diese Z. 44, 459 (1905). 相似文献
20.
Ursula Schmid Paul Gilgen Heinz Heimgartner Hans-Jürgen Hansen Hans Schmid 《Helvetica chimica acta》1974,57(5):1393-1403
Irradiation of 2, 3-diphenyl-2H-azirine ( 1a ) and 1-azido-1-phenyl-propene, the precursor of 2-methyl-3-phenyl-2H-azirine ( 1b ), in benzene, with a high pressure mercury lamp (pyrex filter) in the presence of acid chlorides yields the oxazoles 5a–d (Scheme 2). Photolysis of 2, 2-dimethyl-3-phenyl-2H-azirine ( 1c ) under the same conditions gives after methanolysis the 5-methoxy-2, 2-dimethyl-4-phenyl-3-oxazolines 7a, b, d , while hydrolysis of the reaction mixture leads to the formation of the 1, 2-diketones 8a, c, d (Scheme 4). The suggested reaction path for all these reactions is a 1, 3-dipolar cycloaddition of the photochemically generated benzonitrilemethylides 2 to the carbonyl double bond of the acid chlorides to give the intermediates 4 , followed by either elimination of hydrogen chloride or solvolysis (Schemes 2 and 4). Irradiation of 1c in the presence of acetic acid anhydride leads via the intermediate 9 to the 5-hydroxy-3-oxazoline 10 and the 5-methylidene-3-oxazoline 11 (Scheme 5). 相似文献