全文获取类型
收费全文 | 429709篇 |
免费 | 4790篇 |
国内免费 | 1442篇 |
专业分类
化学 | 235956篇 |
晶体学 | 6259篇 |
力学 | 17886篇 |
综合类 | 10篇 |
数学 | 48531篇 |
物理学 | 127299篇 |
出版年
2020年 | 3010篇 |
2019年 | 3061篇 |
2018年 | 3450篇 |
2017年 | 3387篇 |
2016年 | 6022篇 |
2015年 | 4553篇 |
2014年 | 6383篇 |
2013年 | 18870篇 |
2012年 | 14492篇 |
2011年 | 17810篇 |
2010年 | 11564篇 |
2009年 | 11602篇 |
2008年 | 16646篇 |
2007年 | 16708篇 |
2006年 | 16219篇 |
2005年 | 14806篇 |
2004年 | 13346篇 |
2003年 | 11969篇 |
2002年 | 11739篇 |
2001年 | 14013篇 |
2000年 | 10601篇 |
1999年 | 8372篇 |
1998年 | 6436篇 |
1997年 | 6380篇 |
1996年 | 6355篇 |
1995年 | 5811篇 |
1994年 | 5550篇 |
1993年 | 5299篇 |
1992年 | 6152篇 |
1991年 | 6098篇 |
1990年 | 5749篇 |
1989年 | 5525篇 |
1988年 | 5751篇 |
1987年 | 5465篇 |
1986年 | 5170篇 |
1985年 | 7204篇 |
1984年 | 7297篇 |
1983年 | 5936篇 |
1982年 | 6280篇 |
1981年 | 6170篇 |
1980年 | 5915篇 |
1979年 | 6316篇 |
1978年 | 6381篇 |
1977年 | 6340篇 |
1976年 | 6225篇 |
1975年 | 6027篇 |
1974年 | 5873篇 |
1973年 | 6048篇 |
1972年 | 3651篇 |
1971年 | 2748篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
971.
I. L. Dalinger T. K. Shkineva S. A. Shevelev V. Kral Z. Arnold 《Russian Chemical Bulletin》1993,42(7):1215-1218
The double Vilsmeier formylation of theC-methyl group in pyrazole derivatives has been shown to occur when a nitro-group is in the adjacent position of the ring. A method for the synthesis ofC-(diformylmethyl)nitropyrazoles based on this reaction has been developed.For the previous communication, see Ref. 1; for Part 2, see Ref.2
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1273–1276, July, 1993. 相似文献
972.
Coordination compounds resulting from the interaction of N-(phenyl)benzalaldimine and its derivatives containing a methyl group in different positions of the aniline ring and group(IV) halides, MX4 (where M = Si or Sn and X = Cl or Br), have been prepared and characterized by elemental analyses and electronic, infrared and Raman spectra. 相似文献
973.
T. N. Bowmer E. Reichmanis C. W. Wilkins M. Y. Hellman 《Journal of polymer science. Part A, Polymer chemistry》1982,20(9):2661-2668
Copolymers of methyl methacrylate and 3-oximino-2-butanone methacrylate (OM) were investigated as deep-UV and e-beam resists. Their increased sensitivity relative to PMMA (up to 50 times) was correlated with the radiation chemical yields of the volatile products and main chain scissions. The degradation of these copolymers, activated by the 3-oximino-2-butanone entity, is discussed in terms of energy absorption mechanisms and the subsequent scission reactions. 相似文献
974.
J. Mikuski J. Moravec E. Ochab V. Šára 《Journal of Radioanalytical and Nuclear Chemistry》1981,62(1-2):83-90
The structure of the complex Ag·TBDTPP (tetrabutyl S-dithiopyrophosphate) formed in HNO3 medium was studied by IR and NMR methods. The complex is involved in the isomerization of TBDTPP in the presence of Ag+ and NO
3
−
ions. In the IR spectra, we observe the disappearance of P−O−P band and the occurrence of new absorption bands associated
with P−S−P and P=O bonds. The silver ion is coordinated to the thiophosphoryl group of the isomer molecule. The influence
of HNO3 concentration on complex formation is discussed. 相似文献
975.
Summary The effect of a series of polyacrylic acids, ranging in molecular weight from 1.67×104 to 2.36×106, on the stability of positively charged silver iodide particles has been examined. Flocculation of the sol occurred at a well defined concentration of polyacrylic acid,c
f
, and a further increase in concentration of the polyelectrolyte caused restabilization of the sol. Over the range examinedc
f
appeared to be related to the viscosity average molecular weight of the acid,M
v
, by an equation of the form,c
f
=a ·M
v
– b wherea andb are constants. 相似文献
976.
Abstract— In stationary-phase Escherichia coli B/r, photoreactivation (PR) at 313 nm of ultraviolet (u.v.) killing is inefficient compared with PR at 405 nm, and can be explained solely by photoenzymatic reversal of pyrimidine dimers. In Staphylococcus epidermidis, PR shows a maximum at 313 nm, suggesting that this organism shows the Type III PR proposed by Jagger et al.[5] for Streptomyces strains. Reversal of pyrimidine dimers is not sufficient to explain this PR. The mechanism of Type III PR remains unknown. With both S. epidermidis and E. coli B/r, the amount of uracil–thymine heteroadduct in DNA hydrolysates decreases if the cells are given a post-u.v. treatment at 313 nm, but no decrease is observed if the post-u.v. treatment is at 405 nm. The biological significance of this adduct and of its removal is not clear. It may play a role in Type III PR. 相似文献
977.
J. Eisenbrand und G. Becker 《Fresenius' Journal of Analytical Chemistry》1968,242(3):145-151
Zusammenfassung Es wurde eine direkte Bestimmung des 3,4-Benzpyrens in wä\riger Lösung beschrieben, die auf der Löslichkeitserhöhung beruht, die das in Wasser schwer lösliche 3,4-Benzpyren durch Coffein erfährt. Es können so noch 4 ng/ml bei der angegebenen Standardisierung bestimmt werden. Bei der Direktbestimmung des 3,4-Benzpyrens im System Coffein-Wasser ist ein pH >6,0 einzuhalten, da bei höheren Wasserstoffionenkonzentrationen die Fluorescenzintensität stark abnimmt.
Eine ausführliche Darstellung findet sich in der Dissertation von G. Becker, Univ. Karlsruhe 1968.
Die Messungen zu dieser Arbeit -wurden an dem Chemischen Untersuchungsamt für das Saarland, Saarbrücken, mit einem Spektralphotometer der Deutschen Forschungsgemeinschaft ausgeführt. Beiden Institutionen sind wir zu Dank verpflichtet. 相似文献
Direct fluorimetric determination of benzo(a)pyrene in aqueous medium
A method for the direct determination of benzo(a)pyrene in aqueous solution is based on the increase of its solubility by coffeine. 4 ng of benzo(a)pyrene/ml can be determined by the procedure described. In this direct determination in the system coffeine-water the pH has to be adjusted to >6.0, as the fluorescence intensity considerably decreases with higher H+ concentrations.
Eine ausführliche Darstellung findet sich in der Dissertation von G. Becker, Univ. Karlsruhe 1968.
Die Messungen zu dieser Arbeit -wurden an dem Chemischen Untersuchungsamt für das Saarland, Saarbrücken, mit einem Spektralphotometer der Deutschen Forschungsgemeinschaft ausgeführt. Beiden Institutionen sind wir zu Dank verpflichtet. 相似文献
978.
Following extracorporeal photopheresis (ECP), lymphocytes become apoptotic and upregulate class I MHC antigenic peptides. Conversely, ECP treated monocytes demonstrate activation markers and have an increased avidity for the phagocytosis of apoptotic T cells. Processing of apoptotic T cells by monocytes, following ECP, is thought to induce an immunomodulatory response, which targets untreated, but clonal T cells. Recently we detected apoptotic lymphocytes immediately post ECP. Although enhanced CD95 (Fas) expression has been observed 24 h post ECP, CD95 and Fas-ligand (Fas-L) expression have not been determined at this very early apoptotic stage. Exposure of monocytes to UV has previously suppressed expression of the co-stimulatory molecules required for the presentation of processed antigens to T cells. Our data demonstrate no increase in CD95 or Fas-L expression on T cells tested immediately following ECP. However, the number of T cells expressing Fas-L significantly increased 24 h post ECP (P<0.005). The expression of the co-stimulatory molecules, CD54, CD80 and CD86, remained unaltered on monocytes treated by ECP. Although the mechanism responsible for early induction of lymphocyte apoptosis remains unclear, the later apoptosis involves Fas-L expression. The maintenance of co-stimulatory molecules, on treated monocytes, indicates that they retain the ability to induce an immunomodulatory response. 相似文献
979.
[reaction: see text] Hydrozirconation of alkynes followed by in situ transmetalation to dimethylzinc and 1,2-addition to activated ketones and N-diphenylphosphinoylimines leads to tertiary allylic alcohols and amines in high overall yield. With 8-phenylmenthol as the chiral auxiliary, si-face attack proceeds in good to excellent diastereoselectivities. 相似文献
980.
Catalytic bipotentiometric and biamperometric methods for determining silver(I) with the use of the new manganese(IV)-arsenic(III) indicator reaction catalyzed by iodide ions in the presence of sulfuric acid have been developed. The effects of the sulfuric acid concentration of some ionic species, of the mole ratio of manganese(IV) to arsenic(III) in the solution titrated, and of the titrand temperature, as well as of the current and potential difference, respectively, used for polarization of the indicator electrodes on the conditions for determinations of silver(I) of various concentrations were investigated. The error in the determination of 1.0 g/cm3 silver(I) do not exceed 2%, and the precision of the results is high for both methods. 相似文献