全文获取类型
收费全文 | 60556篇 |
免费 | 15949篇 |
国内免费 | 69篇 |
专业分类
化学 | 65840篇 |
晶体学 | 142篇 |
力学 | 2323篇 |
数学 | 4938篇 |
物理学 | 3331篇 |
出版年
2024年 | 381篇 |
2023年 | 4146篇 |
2022年 | 1506篇 |
2021年 | 2585篇 |
2020年 | 4766篇 |
2019年 | 2505篇 |
2018年 | 2478篇 |
2017年 | 826篇 |
2016年 | 5990篇 |
2015年 | 5886篇 |
2014年 | 5376篇 |
2013年 | 6004篇 |
2012年 | 4313篇 |
2011年 | 2356篇 |
2010年 | 4008篇 |
2009年 | 3787篇 |
2008年 | 2153篇 |
2007年 | 1867篇 |
2006年 | 1126篇 |
2005年 | 1042篇 |
2004年 | 845篇 |
2003年 | 705篇 |
2002年 | 604篇 |
2001年 | 258篇 |
2000年 | 225篇 |
1999年 | 164篇 |
1997年 | 177篇 |
1996年 | 222篇 |
1995年 | 230篇 |
1994年 | 153篇 |
1993年 | 303篇 |
1992年 | 178篇 |
1988年 | 162篇 |
1985年 | 190篇 |
1984年 | 186篇 |
1982年 | 206篇 |
1981年 | 229篇 |
1980年 | 267篇 |
1979年 | 240篇 |
1978年 | 248篇 |
1977年 | 351篇 |
1976年 | 415篇 |
1975年 | 480篇 |
1974年 | 505篇 |
1973年 | 310篇 |
1972年 | 382篇 |
1971年 | 366篇 |
1970年 | 547篇 |
1969年 | 419篇 |
1968年 | 466篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
111.
Aimée Arias-Carbajal Reádigos Roberto Cao Vázquez José R. del Bosque Arin 《Transition Metal Chemistry》1989,14(1):42-44
Summary The electronic properties of a series of cobalt(III)trans-furyldioximato-complexes of the type [CoB(FH)2X] (B=NH3, X=Cl, Br, I or NO2; B=pyridine (py) or thiocarbamide (thio), X=Cl or Br; B=imidazole (imid), X=Br), [Co(FH2)(FH)Cl2] and [Co(thio)2(FH)2]NO3 were studied by i.r., u.v. and1H and13C n.m.r. spectra The results were compared with those from the corresponding dimethylglyoximato-complexes. It was concluded that -conjugation over the equatorial plane in the furyldioximates is greater than in the dimethylglyoximates. There is some evidence of thetrans-influence of the anionic ligands in the ammines which are in the order NO
2
–
>Br–>Cl–. 相似文献
112.
Dr. S. Lal 《Monatshefte für Chemie / Chemical Monthly》1974,105(5):974-976
Study of europium(III)-l-histidine complex has been made in sodium perchlorate at μ=0.1 by tast polarography. The reduction process appears to be quasi irreversible. The apparent rate constants have been determined byGellings method1. With the knowledge ofE 1 2/r and use ofLingane's method, one complex Eu(Histd)2+ with the instability constant 6.77×10?5 is reported. 相似文献
113.
Summary The coagulation concentration for a titania sol decreases if the concentration of a mixture of electrolytes and papain decreases. If the concentration of papain is increased then lesser amount of electrolytes is needed to coagulate the sol. If glycine is added as an additional substance then the value decreases more rapidly. There is no significant change in the pH and the electrical conductance of the sol by the addition of papain or electrolytes. There is a little change, when glycine is added as an additional substance. These observations are explained due to the formation of negative papain ions in a low pH region. The possibility of the adsorption or the release of the counter ions is ruled out.The authors wish to thank Dr.R. C. Mehrotra, Professor and the Head of the Chemistry Department for providing all the facilities for this work. We are also thankful to the Ministry of Education, Government of India, for the award of a research scholarship to one of us (V.K.S.). 相似文献
114.
[reaction: see text] The enzymatic degradation of starch can be monitored electronically using single-walled carbon nanotubes (SWNTs) as semiconducting probes in field-effect transistors (FETs). Incubation of these devices in aqueous buffer solutions of amyloglucosidase (AMG) results in the removal of the starch from both the silicon surfaces and the side walls of the SWNTs in the FETs, as evidenced by direct imaging and electronic measurements. 相似文献
115.
Yingyongnarongkul BE How SE Díaz-Mochón JJ Muzerelle M Bradley M 《Combinatorial chemistry & high throughput screening》2003,6(7):577-587
Advances in high throughput screening (HTS), together with the rapid progress in combinatorial chemistry, genomic and proteomic sciences have dramatically stimulated the development of a variety tools to enable the drug discovery process to become more efficient. Major future challenges in HTS include obtaining high density and good quality data based on assays that are rapid, reliable, inexpensive, sensitive, simple and miniaturised. This paper reviews the development and role of bead-based assays for HTS including DNA and single nucleotide polymorphism (SNP) assays, particularly from a multiplex perspective and evaluating the recent advances in bead-based arrays. The encoding strategies that are commonly used in bead-based assays are highlighted, while the importance of magnetic beads in genomic and proteomic purifications is discussed. In conclusion, bead-based assays offer a powerful promising approach for many aspects of drug discovery. 相似文献
116.
Dr. A. Woppmann 《Monatshefte für Chemie / Chemical Monthly》1974,105(2):419-426
The kinetics of the diazotization of o-, m-, p-chloroaniline in 0.005n- to 0.4n-methanolic HCl-solution at 25, 15, 0, ?10 ?20, and ?30°C was invertigated. It was found that the nitrosation reaction (the same as in1) $$C_6 H_4 ClNH_2 + NOCl \mathop \rightleftharpoons \limits^k C_6 H_4 ClNH_2 NO^ + + Cl^ - $$ is a proceeding advance-back-reaction. The decomposition of C6H4ClNH2NO+ by splitting off a proton is the rate determining step. The free activation enthalpies ΔG * for the nitrosation reaction, the activation entropies ΔS *, the activation enthalpies ΔH * and the activation energiesE a at the given temperatures are calculated. The experimentally found and the calculated velocities are given in Tables 1–6. The equilibrium constants of the o-, m-, p-chloroanilinium ions, and nitrosyl-chloride in methanol are indicated in Table 7, diagram 1. TheK M values (the ionic products of methanol, extrapolated at infinite dilution) together with theK A values of Table 7 give theK B values (p. 2) using the table10. The ΔG B values can be calculated using equation ΔG B = ?RTlnK B Fig 2 shows the linear dependance of the logarithmus of the ΔG * values from the logarithmus of theK B values. 相似文献
117.
The model of Onsager in which a polar molecule undergoes a reaction field due to the polarization of the molecular surroundings is used to evaluate by a S.C.F. calculation (CNDO/2 approximation) the modifications of a molecular structure in the liquid state.Application to water molecule and to three polar dimers for values of the dielectric constant varying between 3 and 78, shows that most of geometric parameters and dipoles moments vary of few per cent when the molecule is inserted in a liquid. In the liquid state dipole moments do not depend very much on the dielectric constant but energies and relative stabilities of isomers are strongly dependent on the medium.[/p] 相似文献
118.
Dr. Marita Fell 《Colloid and polymer science》1967,220(2):107-110
Zusammenfassung Aus einem durch Trypsinabbau von -Keratose erhaltenen Gemisch von Peptiden wurden 15 neutrale, 5 saure und 2 basische Peptide durch Kombination papierchromatographischer und papierelektrophoretischer Methoden getrennt und in sehr geringen Mengen isoliert. Es wurden neben der Aminosäurezusammensetzung 14N-terminale Aminosäuren sowie einige Teilsequenzen in den untersuchten Peptiden ermittelt.Die mittlere Kettenlänge der Peptide beträgt 5,8 Aminosäuren.Mit 1 Tabelle3. Mitt. über Untersuchungen an -Keratose. 2. Mitt.:M. Fell undE. Schnabel, Hoppe-Seyler's Z. physiol. Chem.333, 218 (1963). 相似文献
119.
Dr. R. Franzmair 《Monatshefte für Chemie / Chemical Monthly》1976,107(2):511-520
The reaction of 5-oxo-A-nor-3,5-secocholestan-3-oic acid (1) with simple N-mono and N,N-disubstituted hydrazines including acetylhydrazide was studied. Derivatives of 4-amino-4-aza-cholest-5-ene-3-one (2) were obtained.
Herrn Prof. Dr.H. Bretschneider mit den besten Wünschen zum 70. Geburtstag gewidmet. 相似文献
Herrn Prof. Dr.H. Bretschneider mit den besten Wünschen zum 70. Geburtstag gewidmet. 相似文献
120.
Dr. Ing. K. Baaz 《Colloid and polymer science》1970,236(2):154-163
Zusammenfassung Die tertiären n-aliphatischen Phosphine spreiten auf Wasser spontan zu einem monomolekularen Film aus. Die Kompressionsisothermen der untersuchten tertiären aliphatischen Phosphine in homologer Reihe mit der Kettenlänge von C4 bis C16 wurden ausgemessen und die dabei auftretenden Filmzustände identifiziert. Das tertiäre C5-Phosphin bildet realgasanaloge, die C6–C12-Phosphine flüssiganaloge und die längerkettigen Phosphine festanaloge Filme.Ein Übergang vom tertiären Phosphin zum Phosphinoxid hat auf die Filmbildung keinen Einfluß, es ergibt sich nur eine geringfügige Vergrößerung der molekularen Fläche von etwa 10%.Der auf den Filmdruck 0 extrapolierte molekulare Flächenbedarf wurde sowohl nach den herkömmlichen Verfahren aus denF/A-Diagrammen als auch mit einer anderen Methode aus denF·A/F-Isothermen berechnet: beide Werte zeigen sehr gute Übereinstimmung. Dabei zeigt der Vergleich mit dem aus den molekularen Abmessungen errechneten Flächenbedarf, daß die Phosphinmoleküle im komprimierten Film nicht vollständig in Pyramiden- bzw. Kegelform geordnet sind sondern daß die aliphatischen Ketten vom sechsten C-Atom an senkrecht auf der Substratoberfläche stehen. Der P-C-Winkel ist nicht für, die ganze Kette richtungsweisend, die flexiblen Kohlenwasserstoff ketten sind abgewinkelt. Mit zunehmender Kettenlänge wächst das Molekül nur noch senkecht in die Höhe, deshalb bleibt die molekulare Fläche ab C6 annähernd konstant.
Mit 8 Abbildungen und 5 Tabellen 相似文献
Summary Tertiäry n-aliphatic phosphines form on water surfaces spontanously monolayers. The force-area isotherms of a homologous series of phosphins with a chainlength varying from C4 to C16 were measured and the appearing states of the films were identified. The tertiary C5 phosphine forms real-gas analogous films, the C6 to C12 phosphines liquid, analogous films and phosphines with lange carbon chains solid analogous films.A transition from tertiäry phosphines to the corresponding phosphine oxide has no influence on the formation of the films, it results only in an insignificant (10 p. c.) increase of the molecular area.The molecular area from the extrapolation to the film pressure of 0 was calculated by the customery methods out of theF/A diagramms, and by an other methods out of theFA/F isotherms. Good accordance of both values is shown. The area calculated from the molecular dimensions shows in comparison, that the phosphine molecules in comprimated films are not exactly disposed in pyramidal or conic shape, but that each aliphatic chain changes its direction after the sixth C-atom and stands vertically to the liquid-air interface. The direction of the chains is not determined by the angle of the P–C bonding, because the flexible carbon changes are distorted. With increasing chainlength, beginning from the tertiäry C6 phosphin the carbon chains stand only vertically to the substrate. Therefore the need of molecular area remains almost constant.
Mit 8 Abbildungen und 5 Tabellen 相似文献