全文获取类型
收费全文 | 660篇 |
免费 | 12篇 |
国内免费 | 3篇 |
专业分类
化学 | 394篇 |
晶体学 | 19篇 |
力学 | 19篇 |
数学 | 150篇 |
物理学 | 93篇 |
出版年
2021年 | 6篇 |
2020年 | 6篇 |
2019年 | 7篇 |
2018年 | 6篇 |
2017年 | 11篇 |
2016年 | 9篇 |
2015年 | 10篇 |
2014年 | 30篇 |
2013年 | 45篇 |
2012年 | 14篇 |
2011年 | 27篇 |
2010年 | 10篇 |
2009年 | 12篇 |
2008年 | 16篇 |
2007年 | 21篇 |
2006年 | 12篇 |
2005年 | 21篇 |
2004年 | 19篇 |
2003年 | 18篇 |
2002年 | 16篇 |
2001年 | 16篇 |
1999年 | 6篇 |
1995年 | 10篇 |
1993年 | 8篇 |
1992年 | 8篇 |
1991年 | 14篇 |
1990年 | 10篇 |
1989年 | 13篇 |
1988年 | 6篇 |
1987年 | 20篇 |
1986年 | 9篇 |
1985年 | 6篇 |
1984年 | 17篇 |
1983年 | 12篇 |
1982年 | 16篇 |
1981年 | 12篇 |
1980年 | 12篇 |
1979年 | 9篇 |
1978年 | 8篇 |
1977年 | 10篇 |
1976年 | 6篇 |
1975年 | 8篇 |
1974年 | 10篇 |
1973年 | 7篇 |
1972年 | 8篇 |
1970年 | 6篇 |
1963年 | 5篇 |
1957年 | 5篇 |
1942年 | 8篇 |
1941年 | 5篇 |
排序方式: 共有675条查询结果,搜索用时 141 毫秒
1.
2.
3.
T. K. V. Iyengar N. Srinivasacharyulu J. V. Ramana Murthy 《Zeitschrift für Angewandte Mathematik und Physik (ZAMP)》1988,39(5):649-667
An elliptic cylinder is performing oscillations parallel to either of the principal axes of the cross-sectional ellipse in a fluid particle suspension. The stream function governing the flow and the velocity components are determined in terms of Mathieu functions. The drag on the cylinder is evaluated and expressed in terms of two parametersK andK. The effects of the variation of the frequency parameter, eccentricity parameter and relaxation time parameter on the drag parametersK, K is studied numerically. 相似文献
4.
The monohydroboration of caryophyllene with dicyclohexylborane followed by oxidation brought about the participation of the (E)-trisubstituted double bond in preference to the exocyclic double bond during hydroboration to the corresponding unsaturated alcohol. This alcohol gave the corresponding ketone by oxidation. Isocaryophyllene under similar conditions provided the unsaturated alcohol as the major product, wherein the participation of the exocyclic double bond took place during hydroboration. Our attempts to achieve cyclic hydroboration with caryophyllene or isocaryophyllene using thexylborane resulted in the formation of the corresponding unsaturated alcohol. We achieved partial regioselective reduction of caryophyllene and isocaryphyllene with diimide to produce the corresponding dihydroderivative. 相似文献
5.
It has been noticed that the major part of the loss of ?H from the molecular ion of most of the o-methoxythioamides results from an ortho effect of the methoxy group. Comparison of the MIKE spectra of the [M? SH]+ of 1-(2-methoxyphenylthioxomethyl)piperidine and 1-(2-methoxyphenylthioxomethyl)pyrrolidine with the MIKE spectra of [M? SH]+ of the corresponding unsubstituted compounds, reported earlier, indicated two parallel pathways for the formation of [M? SH]+ in the o-methoxy compounds. In the first pathway, as has been noticed in thioamides in general, the loss of ?H involves the migration of either the α-hydrogen in the amine moiety or the hydrogen attached to nitrogen. In the second pathway, the migration of a hydrogen from the o-methoxy group to the sulphur atom followed by ejection of SH from the molecular ion leads to a stable cyclized ion. Interesting secondary fragmentations as a consequence of this ortho effect have also been noticed. 相似文献
6.
S. R. Sagi M. S. Prasada Rao Karri V. Ramana 《Journal of Thermal Analysis and Calorimetry》1981,20(1):93-100
The effect of the thallium(I) concentration on the potentiometric titration of thallium(III) with oxalic acid in 0.1M HNO3 or 0.05M H2SO4 is studied, and conditions are established for the preparation of the thallium(I) bis-oxalato diaquo thallate(III) complex. Chemical analysis of the salt corresponds to the formula T1I(T1III(C2O4)2) · 5 H2O. Thermal decomposition studies on the complex using TG, DTG and DTA techniques indicate the formation of thallium(I) oxalate (stable from 130° to 320°) as the intermediate, the final product being a mixture of thallium(I) oxide and thallium(III) oxide (stable from 520° to 600°). Infrared absorption spectra, X-ray diffraction patterns and microscopic observations are used to characterise the complex and the intermediate. 相似文献
7.
Summary Two methods for the determination of ascorbic acid are described. The first employs titration with iodate in presence of cyanide and hydrochloric acid and starch indicator with two end points, corresponding to the formation of iodine after reduction to iodide and conversion of iodine to iodine cyanide respectively. The titration is applied to the indirect determination of vanadium(V). In the second method ascorbic acid is treated with excess ferric solution and the ferrous iron formed is determined colorimetrically by ortho-phenanthroline.
Zusammenfassung Zwei Verfahren zur Ascorbinsäurebestimmung werden beschrieben. Bei dem ersten wird in Gegenwart von KCN und Salzsäure sowie von Stärke als Indicator mit Jodatlösung titriert. Dabei werden zwei Endpunkte erhalten, die der Reduktion von Jodat zu Jodid und damit verbundener Jodbildung bzw. der Umwandlung des Jods in JCN entsprechen. Diese Titration wird auch zur indirekten Bestimmung von Vanadium(V) verwendet. Bei dem zweiten Verfahren wird die Ascorbinsäure mit überschüssiger Eisen(III)-lösung behandelt und das gebildete zweiwertige Eisen colorimetrisch mit o-Phenanthrolin bestimmt.相似文献
8.
From the measurements of conductivity, diffusion coefficient etc., Jander indicated the presence of several isopoly-anions of molybdenum under different pH conditions. He and subsequent workers in the field dealt with solutions only. In the present work one free molybdic acid, and one ammonium acid molybdate were isolated in solid condition at pH 4.6 and 2. On analysis, their compositions were found to be H4Mo3O11 and NH4H5Mo6O21 (or (NH4)2H4Mo7O24) respectively. 相似文献
9.
The intramolecular cycloaddition of the previously described azidoalkene 16 , the related diacetates 7 and 13 , and the monoacetate 8 led diastereoselectivity to the (2R)- and (2S)-configurated hydropyridotriazoles 17 , 9 and 11 , 14 and 15 , and 10 and 12 , respectively (Scheme 1). Thermolysis of 16 gave also the aziridine 18 , its proportion increasing with reaction time. The diastereoselectivity of the cycloaddition- is rationalized on the basis of steric interactions and of H? bonds in the transition state. Photolysis in benzene partially transformed 9 into the aziridine 19 . Treatment of 9 with aqueous AcOH gave 19 and the tetrahydrofuran 20 , with AcOH in benzene 20 and the triacetate 23 , and with aqueous H2SO4 in THF, the primary alcohol 22 (room temperature) or 19 and 22 (0°). Deacetylation of 9 followed by reaction with pyridinium hydrochloride led to the tetrahydrofuran 21 and the chloride 24 (Scheme 2). The diacetate 22 and the triacetate 23 gave the tripl 25 which was deprotected to 26 . Reduction of the keto-aziridine 18 (NaBH4) gave the alcohols 27 and 29 which were acetylated to give 28 and 19 , respectively (Scheme 3). Treatment of the aziridine 28 with AcOH in benzene followed by deacetylation gave 30 and hence 31 . AcOH in benzene transformed the triazoline 15 first into the aziridine 32 and hence into 33 , which was deprotected to give the triol 34 and hence 35 . The 2-(hydroxymethyl)piperidines 26 , 31 , and 35 inhibited Vibrio cholerae sialidase with K1 = 3.8 · 10?2 M, 3.4 · 10?3 M, and 1.5 · 10?4 M, respectively. The conformation of the glycerol side chain of these compounds and of the unbranched piperidines 2–4 deviates from the one of Neu5Ac (and Neu2en5Ac). This finding is rationalized by an H-bond between OH? C(8) and NH? C(6). The conformations and the K1 values of 26 , 31 , and 35 correlate with each other. 相似文献
10.
Titrimetric and spectrophotometric methods have been developed for the determination of hydrogen peroxide at mmole and mumole levels respectively. In these methods thallium(III) is used as the oxidant and the reduced thallium(I) is determined oxidimetrically with potassium bromate in the titrimetric method and by measuring the absorbance of thallium(III) at 260 nm in the presence of 0.1M hydrochloric acid and 1M perchloric acid in the spectrophotometric method. Photochemical redox methods for the estimation of hydrogen peroxide in the presence of a number of diverse ions are described. 相似文献