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91.
Islas-González G Benet-Buchholz J Maestro MA Riera A Pericàs MA 《The Journal of organic chemistry》2006,71(4):1537-1544
Upon treatment with BF3.Et2O at low temperature, enantiopure benzyl-type ethers of arylglycidols with electron withdrawing substituents at the skeletal aryl group and electron donating substituents at the benzyl group undergo stereospecific rearrangements of Friedel-Crafts type, leading to enantiopure 4-diarylmethyl-1,3-dioxolanes (2) or to enantiopure trans-4,5 disubstituted tetrahydrobenzo[c]oxepin-4-ols (5). The course of the reactions is controlled by the substitution pattern at the benzyl ether: While benzylic systems activated toward ipso substitution afford diarylmethanes 2 through a Friedel-Crafts reaction followed by fragmentation, benzylic systems activated toward ortho attack lead to enantiopure oxepinols 5 through a 7-endo-tet ring closure of Friedel-Crafts type. 相似文献
92.
The reaction of fac-[ReBr(CO)3(NCMe)2] (1) with either pyrazole (Hpz) or 3,5-dimethylpyrazole (Hdmpz) in a 1:2 Re/pyrazole ratio affords the known complexes fac-[ReBr(CO)3(Hpz)2] (2) and [ReBr(CO)3(Hdmpz)2] (3). Using a 1:1 ratio, MeCN as solvent, and longer reaction times led to a mixture in which the major components are the pyrazolylamidino complexes fac-[ReBr(CO)3(HN=C(CH3)pz-kappa2N,N)] (4) and fac-[ReBr(CO)3(HN=C(CH3)dmpz-kappa2N,N)] (5). The complexes fac-[ReBr(CO)3(Hpz)(NCMe)] (6) and fac-[ReBr(CO)3(Hdmpz)(NCMe)] (7) (along with 2 and 3) were found to be minor components of these reactions. Analogous reactions of fac-[Re(OClO3)(CO)3(NCMe)2] yielded fac-[Re(NCCH3)(CO)3(HN=C(CH3)pz-kappa2N,N)]ClO4 (8), fac-[Re(NCCH3)(CO)3(HN=C(CH3)dmpz-kappa2N,N)]ClO4 (9), fac-[Re(Hpz)(CO)3(HN=C(CH3)pz-kappa2N,N)]ClO4 (10), and fac-[Re(Hdmpz)(CO)3(HN=C(CH3)dmpz-kappa2N,N)]ClO4 (11). The X-ray structure of 11 showed the perchlorate anion to be hydrogen-bonded by the N-H groups of the pyrazole and pyrazolylamidino ligands. The behavior of the compound fac-[Re(Hdmpz)(CO)3(HN=C(CH3)dmpz-kappa2N,N)]BAr'4 (13) (synthesized by reaction of [ReBr(CO)3(Hdmpz)2] (3) with (i) AgOTf and (ii) NaBAr'(4)/MeCN) as an anion receptor has been studied in CD3CN solution. In addition, the structure of the supramolecular adduct fac-[Re(CO)3(Hdmpz)(HN=C(CH3)dmpz-kappa2N,N)].Cl (14), featuring chloride binding by the two N-H groups, was determined by X-ray diffraction. 相似文献
93.
94.
Gerbino DC Hevia E Morales D Clemente ME Pérez J Riera L Riera V Miguel D 《Chemical communications (Cambridge, England)》2003,(3):328-329
A new basic transformation linking two important classes of transition metal compounds; namely, hydroxo and hydrosulfido complexes has been discovered. 相似文献
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98.
Vera L. P. Soares L. N. Batista Rosane A. S. San Gil 《Journal of Thermal Analysis and Calorimetry》2007,87(3):805-809
MgO was
incorporated into montmorillonite (MMT) though the controlled formation of
Mg(OH)2 followed by calcination. The evidence for Mg2+
in MMT before calcination was concluded from TG curves where two different
temperature ranges for Mg(OH)2 dehydroxylation suggested that the location
of Mg2+ at its internal and external surfaces.
FTIR by diffuse reflectance technique of calcined sample showed a typical
MgO band. XRD indicated a decrease in structural order and no collapse of
clay structure. The organic compounds adsorption to MMT modified with MgO
as suggested by increased degradation temperatures occurred at internal and
external clay surfaces besides in an area formed probably by MgO and MMT layers. 相似文献
99.
We analyze the theoretical basis of a procedure to determine an unknown normalization factor in discretized wave functions, which we have successfully used in a series of calculations of resonance widths for atomic and molecular systems. By reducing this determination to that of a suitable interpolation function for the energy eigenvalues, the problem is easily solved when atomic basis sets are chosen according to simple rules. Illustrations of our procedure are presented for atomic, molecular, and model systems; renormalized wave functions are compared with the exact ones for these model systems. The resulting method of renormalized continuum wave functions has a wide range of application in the study of long-lived quasibound states (predissociation, autoionization, photoionization, unimolecular reactions, etc.). 相似文献
100.
Ion-exchange resins have been often used as catalysts especially those based on styrene-divinylbenzene copolymers with sulfonic acid groups in the aromatic rings of polymer chains. That is due to the advantages of heterogenous catalysis over the homogeneous acid catalysis. Moreover, resin catalysts can often lead to high selectivity in organic reactions due to the matrix effects. Therefore, the study of copolymers synthesis conditions to determine the type of polymer structure produced as well as the characterization of sulfonic resins obtained thereof are of great interest. The current paper describes the synthesis, characterization and evaluation as catalysts of sulfonic resins derived from polymer supports synthesized by aqueous suspension polymerization of styrene and divinylbenzene. The reaction conditions were varied and polymer supports with different physical properties and morphological characteristics were obtained. The polymer supports were chemically modified by sulfonation. The resultant sulfonic resins had their catalyst activity evaluated in the esterification of acetic acid with n-butanol. 相似文献