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971.
972.
N. Grassie J. Gilks T. Moodie P. Quietsch P. Riordan 《Journal of polymer science. Part A, Polymer chemistry》1973,11(9):2287-2294
In the presence of SnCl4 in 1,2-dichloroethane solution, copolymers of styrene and methyl methacrylate undergo a Friedel-Crafts acylation reaction between the ester groups and the ortho position of adjacent styrene units to form a partial ladder polymer. This has been confirmed by infrared and ultraviolet spectral analysis and by observing the influence of substituted styrenes on the rate of the reaction. A similar reaction can be induced to occur between polystyrene and poly(methyl methacrylate). Thermal analysis measurements demonstrate that the degradation properties of copolymers of styrene and methyl methacrylate are profoundly changed by this treatment. 相似文献
973.
974.
R. F. B. Serpa E. F. O. De Jesus M. J. Anjos R. T. Lopes M. G. T. do Carmo S. Moreira M. S. Rocha A. M. B. Martinez 《Journal of Radioanalytical and Nuclear Chemistry》2006,269(3):647-652
Summary The study of trace element levels is of great importance due to their relevance in agingand several neurodegenerative diseases.
This work compares the elemental concentrations in different postnatal ages and between the temporal cortex, entorhinal cortex
and hippocampus from Wistar rats, using X-ray total reflection fluorescence with synchrotron radiation. Ten elements were
determined in brain samples: Ti, Cr, Mn, Fe, Cu, Zn, (at trace level) and P, S, Cl and K (at major levels). The elements that
increased with aging in cortical areas were: S, K, Fe, Cu and Zn. Ca and Zn levels decreased with advancing age in the hippocampus.
In addition to this, Ti, Mn and Fe levels were more conspicuous in the entorhinal cortex. 相似文献
975.
I. Trapp T. Famulok U. Risse A. Kettrup 《Fresenius' Journal of Analytical Chemistry》1998,362(4):409-414
Due to the complex composition of metal working fluids (MWF) the determination of all individual compounds is sometimes difficult
and very expensive. Today the widely used method for the quantification of airborne MWFs consists of a non specific IR analysis
of their C-H valence bands. With a new design of sample cell this inexpensive technique was extended to a more detailed screening
of the MWF composition, especially the detection of carbonyl compounds in MWFs and their aerosols and vapors. The screening
method was evaluated for the determination of concentrations of the aldehyde nonanal and the ketone diacetone alcohol in air
in laboratory experiments. In preliminary workplace studies the applicability of this method to the (semi-)quantitative determination
of carbonyl compounds in airborne MWFs is shown. The screening method was found to be very useful, specially to detect alterations
in the composition of the MWF due to industrial use.
Received: 16 January 1997 / Revised: 9 April 1998 / Accepted: 14 April 1998 相似文献
976.
Andrew L. Sargent Mark E. Rollog Cassandra T. Eagle 《Theoretical chemistry accounts》1997,97(1-4):283-288
Fenske-Hall molecular orbital calculations have been applied to a new, structurally isolable analog of the intermediate involved
in catalytic rhodium carboxylate carbenoid transformations. Results from the structural characterization of axially ligated
rhodium acetate phenylisonitrile complexes have been utilized in approximate molecular orbital calculations. The results from
the calculations suggest that a significant degree of π back-bonding exists between the metal and isonitrile fragments which,
by analogy, implies that π back-bonding should also exist in the rhodium carbenoid intermediate. Sensitivity of the Fenske-Hall
method to the magnitude of π back-donation in these complexes was gauged through calculations involving different phenylisonitrile
groups in which the π back-bonding ability was modulated through derivativization. The reliability of the Fenske-Hall method
was evaluated through a comparison to a high-level calculation.
Received: 13 December 1996 / Accepted: 18 March 1997 相似文献
977.
Mitomycin C, an anti-neoplastic agent, was covalently attached to bovine serum albumin through various kinds of spacers such as glutaryl, succinyl, trans-aconityl, methylsuccinyl and the trimellityl group. The prior acylation of albumin not only prevented protein polymerization in the presence of carbodiimide, but also increased the extent of conjugation of the drug. The conjugate of mitomycin C-glutarylated albumin showed the best properties among the conjugates prepared in meeting the requirements for a high yield of nonpolymerized product with an adequately high mitomycin C content and stability as a macromolecular prodrug. 相似文献
978.
A high-performance liquid chromatographic method was developed for the determination of citrulline and homocitrulline using a post-column colorimetric reaction with o-phthaladehyde and N-(1-naphthyl)-ethylenediamine. Citrulline and homocitrulline were determined with no interferences from protein amino acids. The results show that the level of citrulline in the plasma of patients with uremia on intermittent hemodialysis is higher than that in healthy human plasma, and that homocitrulline is excreted into the urine of healthy adults. 相似文献
979.
E. J. Land A. Thompson T. G. Truscott K. V. Subbarao M. R. Chedekel 《Photochemistry and photobiology》1986,44(6):697-702
The photochemistries of the melanin precursors dopa, 5-S-cysteinyldopa (5-SCD) and 2.5-S,S'-dicysteinyldopa (2.5-SCD) were investigated by 265-nm laser flash photolysis. The quantum yield of hydrated electron following flash photolysis of dopa (9.1%) was half the yield of dopasemiquinone (19.6%), implying that dopasemiquinone is formed via two primary photochemical mechanisms: photionisation (giving e) or photohomolysis (giving H˙ ). Dopasemiquinone rapidly disproportionates to form dopaquinone and re-form dopa. Dopaquinone in turn decays via a base-catalysed unimolecular cyclisation eventually to form dopachrome. Assignment of the transient species was confirmed by previous pulse radiolysis studies of the one-electron oxidation of dopa. In contrast, flash photolysis of the cysteinyldopas, 5-SCD and 2,5-SCD results in lower photoionisation quantum yields and the production of initial transient species whose absorption spectra were markedly different from their semiquinone absorption spectra previously determined pulse radiolytically. These observations indicate that the primary cysteinyldopa photochemical species is not such a semiquinone, but rather results from S-CH2 bond photohomolysis. Absorption spectra and rate constants for the formation and decay of various transient species are reported. 相似文献
980.
The cytotoxic natural product dendrodoine has been synthesised by a 1,3-dipolar addition reaction between indolyl-3-carbonyl nitrile and N,N-dimethylaminonitrile sulphide generated through the thermolysis of 5-(N,N-dimethylamino)-1,3,4-oxathiazol-2-one. 相似文献