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Johannes P. C. Vissers Henk A. Claessens Pavel Coufal 《Journal of separation science》1995,18(9):540-544
Retention factors in capillary electrochromatography (CEC) were calculated by means of theoretically derived equations and experimentally determined parameters in microcolumn liquid chromatography and capillary zone electrophoresis. It was found that the retention factor of uncharged components in CEC was about 20% higher than was calculated. The derived equations do not take into account alteration of the nature of the stationary phase or distribution constant by the applied electric field. However, the influence of the electric field on the retention in CEC can be estimated. Individual field contributions could not be determined. 相似文献
55.
Summary A method for the separation of a number of herbicides consisting of chlorophenoxy acids by micellar electrokinetic capillary chromatography (MECC) was developed. Sodium dodecyl sulphate (SDS), Brij 35, cetyltrimethylammonium bromide (CTAB) and methanol were introduced into the buffers to investigate their effects on the separation of the herbicides. SDS combined with Brij 35 as the micellar agent was found to provide the best overall separation of these components. 相似文献
56.
Claessens CG González-Rodríguez D Torres T Martín G Agulló-López F Ledoux I Zyss J Ferro VR García de la Vega JM 《The journal of physical chemistry. B》2005,109(9):3800-3806
Second order nonlinear optical properties of a series of trinitrosubphthalocyanine (SubPc) isomers were studied experimentally by electric field induced second harmonic (EFISH) generation and hyper Rayleigh scattering (HRS). These experimental values were compared to the ones obtained theoretically employing both sum over states (SOS) and finite field (FF) methods. From these studies, it was shown that the dipolar contributions to the beta tensor are very much dependent on the substitution pattern at the periphery of the subphthalocyanine macrocycle, whereas the octupolar contributions remain mostly unchanged. Consequently, it was deduced that SubPc is extremely well suited for the decoupling of octupolar and dipolar contribution to the NLO response. 相似文献
57.
Summary Methods to determine the contribution of the chromatographic equipment to the total band broadening which involve replacing
the column by a union or a capillary tube are not suitable as they involve a fundamental change in the chromatographic system.
The linear extrapolation method, based on the estimation of the relative influence of the instrument variance on solutes with
different capacity factors, is a more attractive alternative method since the column remains in the chromatographic system.
This method is only valid when a number of conditions are satisfied. By meeting these conditions the error in the instrument
variance by using the linear extrapolation method was determined. At the same time, ways to minimise these errors were studied.
Use of the linear extrapolation method in combination with conventional columns of 4.6 mm i.d. appears to yield inaccurate
results.
In combination with microbore columns the method can be used, provided the columns have a maximum length of 5cm and contain
a packing material with a particle size of 2 or 3μm. The error in the determined instrument variance is then of the order
of 2μl2. 相似文献
58.
Butylacrylate – styrene co-polymers prepared by atom transfer radical polymeratization were separated on an octadecyl silica column by gradient elution with tetrahydrofuran in water, up to the molar masses 10,000. In reversed-phase high performance liquid chromatography (RP-HPLC), the retention of macromolecules is affected very significantly even by change of a few tenths of per cent of the organic solvent in the aqueous-organic mobile phase. Therefore, gradient elution was used for the determination of the parameters of the equations describing the effects of the mobile phase on the retention behaviour of synthetic polymers. The retention parameters of homopolymers and copolymers were calculated from the gradient data using two retention models. The retention behaviour of the copolymers was described using the experimental gradient retention data for homopolymers. 相似文献
59.
A series of new unsymmetrically substituted subphthalocyanines containing iodo or octylthioether substituents on the outer aromatic rings have been synthesized. The statistical reaction of one equivalent of 1,2-dicyano-3-iodobenzene whether with two equivalents of 1,2-dicyano-4-octylthiobenzene or with two equivalents of 1,2dicyano-4,5-dioctylthiobenzene in the presence of boron trichloride in 1-chloronaphthalene yielded in both cases all the possible expected unsymmetrically substituted subphthalocyanines, which were separated by column chromatography on silica gel. All compounds were identified by FAB mass spectrometry and then characterized by HR-LSIMS spectrometry. The unambiguous characterization of each constitutional isomer was made possible by careful examination of the symmetry environment experienced by each proton on their 1H-NMR spectra. 相似文献
60.
Optimisation and characterisation of silica-based reversed-phase liquid chromatographic systems for the analysis of basic pharmaceuticals 总被引:1,自引:0,他引:1
Vervoor RJ Debets AJ Claessens HA Cramers CA de Jong GJ 《Journal of chromatography. A》2000,897(1-2):1-22
Reversed-phase liquid chromatography using silica-based columns is successfully applied in many separations. However, also some drawbacks exist, i.e. the analysis of basic compounds is often hampered by ionic interaction of the basic analytes with residual silanols present on the silica surface, which results in asymmetrical peaks and irreproducible retention. In this review, options to optimise the LC analysis of basic pharmaceutical compounds are discussed, i.e. eluent optimisation (pH, silanol blockers) and stationary phase optimisation (development of new columns with minimised ionic interactions). The applicability of empirical based, thermodynamically based and test methods based on a retention model to characterise silica-based reversed phase stationary phases, as well as the influence of the eluent composition on the LC analysis of basic substances is described. Finally, the applicability of chemometrical techniques in column classification is shown. 相似文献