全文获取类型
收费全文 | 398篇 |
免费 | 9篇 |
专业分类
化学 | 216篇 |
晶体学 | 1篇 |
力学 | 9篇 |
数学 | 53篇 |
物理学 | 128篇 |
出版年
2023年 | 4篇 |
2022年 | 11篇 |
2021年 | 5篇 |
2020年 | 15篇 |
2019年 | 13篇 |
2018年 | 9篇 |
2017年 | 6篇 |
2016年 | 9篇 |
2015年 | 11篇 |
2014年 | 13篇 |
2013年 | 28篇 |
2012年 | 16篇 |
2011年 | 26篇 |
2010年 | 12篇 |
2009年 | 14篇 |
2008年 | 12篇 |
2007年 | 14篇 |
2006年 | 22篇 |
2005年 | 9篇 |
2004年 | 9篇 |
2003年 | 8篇 |
2002年 | 6篇 |
2001年 | 5篇 |
2000年 | 7篇 |
1998年 | 3篇 |
1996年 | 4篇 |
1995年 | 2篇 |
1994年 | 3篇 |
1993年 | 2篇 |
1992年 | 2篇 |
1991年 | 4篇 |
1990年 | 3篇 |
1989年 | 3篇 |
1988年 | 4篇 |
1986年 | 6篇 |
1985年 | 5篇 |
1984年 | 6篇 |
1983年 | 5篇 |
1982年 | 4篇 |
1981年 | 5篇 |
1980年 | 7篇 |
1979年 | 14篇 |
1978年 | 6篇 |
1977年 | 8篇 |
1976年 | 5篇 |
1975年 | 5篇 |
1974年 | 3篇 |
1973年 | 4篇 |
1972年 | 3篇 |
1963年 | 1篇 |
排序方式: 共有407条查询结果,搜索用时 93 毫秒
1.
Dielectric relaxation study of the binary mixtures of poly(vinyl pyrrolidone) (PVP) (Mw=24000, 40000 and 360000 g mol−1) with ethyl alcohol (EA) and poly(ethylene glycol)s (PEGs) (Mw=200 and 400 g mol−1) in dilute solutions of dioxane were carried out at 10.1 GHz and 35°C. The relaxation time of PVP-EA mixtures was interpreted
by the consideration of a wait-and-switch model in the local structure of self-associated ethyl alcohol molecules and also
the PVP chain length as a geometric constraint for the reorientational motion of ethyl alcohol molecules. The formation of
complexes and effect of PVP chain length on the molecular dynamics, chain flexibility and stretching of PEG molecules in PVP-PEG
mixtures were explored from the comparative values of dielectric relaxation time. Further, relaxation time values in dioxane
and benzene solvent confirm the viscosity independent molecular dynamics in PVP-EA mixtures but the values vary significantly
with the non-polar solvent environment. 相似文献
2.
Upadhyay R. K. Bansal Rashmi R. Vajpai Usha 《Monatshefte für Chemie / Chemical Monthly》1976,107(5):1221-1225
Thin layer chromatographic behaviour of ten anils was studied on silica gel adsorbent mixed with starch binder with ten solvent systems. Simultaneous separation, identification and determination of ternary mixtures of isomers was stressed. TheR
F
increasing order was found to be dependent on the solvent and independent of the degree of saturation of the chamber. The correlations ofR
F
with max and (C=O) of isomers were established and used in their identification. Six anils were separated in methanol—benzene (11). 相似文献
3.
The microgram detection and determination of picric acid with sodium hypochlorite solution is based on its oxidation in alkaline solution and chlorination with excess of chlorine present in hypochlorite solution. A characteristic orange color is obtained, which can be used as a specific test. The sensitivity of the picric acid was enhanced by performing the resin spot test. This color reaction was applied for the determination of picric acid spectrophotometrically. 相似文献
4.
Validation of LC/MS electrospray ionisation method for the estimation of ursodiol in human plasma and its application in bioequivalence study 总被引:1,自引:0,他引:1
Sundd Singh S Shah H Gupta S Jain M Sharma K Patel H Shah B Thakkar P Patel N Shah R Bhushan Lohary B 《Annali di chimica》2004,94(12):951-959
A novel High Performance Liquid Chromatography-electrospray mass spectrometric method has been developed for the estimation of Ursodiol (Ursodeoxycholic acid)--a bile acid, in human plasma using Ornidazole as internal standard. The methodology involved solid phase extraction of the analyte from human plasma matrix. The chromatographic separation was achieved within seven minutes by an isocratic mobile phase containing 1.0 mM ammonium acetate and Acetonitrile (65:35, v/v), flowing through XTerra MS C18, 100 x 2.1, 3.5 microm analytical column, at a flow rate of 0.2 ml/min. Ion signals were measured in negative mode for Ursodiol and internal standard at m/z 391.3 and 278.1, respectively. A detailed validation of the method was performed as per USFDA guidelines and the standard curves were found to be linear in the range 50.0 ng/ml to 3000.0 ng/ml with the mean correlation coefficient more than 0.99. The absolute recovery was more than 54.90% for Ursodiol and 76.51% for internal standard. Ursodiol was stable for sixty-nine days at -70 degrees C and for eight hours at ambient temperature. After extraction from plasma, the reconstituted samples of Ursodiol were stable in autosampler at 10 degrees C for forty-eight hours. Upon subjecting to three freeze thaw cycles, there was no change in the recovery of the analyte. The integrity of the plasma samples remained unaffected even upon four-fold dilution with drug free human plasma. The method was simple, specific, sensitive, precise, accurate and suitable for bioequivalence and pharmacokinetic studies. It was successfully applied to the pilot bioequivalence study of Ursodiol in male human subjects. 相似文献
5.
Michael additions of a β,γ-unsaturated ester and a nitrile to a variety of α,β-unsaturated ketones can be effected with high regioselectivity and in good yields using P(i-PrNCH2CH2)3N as a catalyst. 相似文献
6.
A procedure has been developed for the direct fourth-derivative spectrophotometric determination of iron(III) dimethyldithiocarbamate by converting it into an iron(II) 2,2'-bipyridyl complex, which is then dissolved in Triton X-100. Beer's law is obeyed over the concentration range 0.5-20 microg mL(-1 )in the final solution. Various parameters such as the effect of pH and interference of large number of ions on the determination of ferbam have been studied in detail. The method is sensitive, highly selective and can be used for the determination of ferbam in a commercial sample and in mixtures with various dithiocarbamates (ziram, zineb, maneb, etc.) and from wheat grains. 相似文献
7.
Preparation and some reactions of the first cumulated ylide of arsenic, viz. triphenylarsoranylideneketene are described. 相似文献
8.
Sanyal A Rautaray D Bansal V Ahmad A Sastry M 《Langmuir : the ACS journal of surfaces and colloids》2005,21(16):7220-7224
We show here that reaction of the fungus, Fusarium oxysporum, with the aqueous heavy-metal ions Pb2+ and Cd2+ results in the one-step formation of the corresponding metal carbonates. The metal carbonates are formed by reaction of the heavy-metal ions with CO2 produced by the fungus during metabolism and thus provide a completely biological method for production of crystals of metal carbonates. The PbCO3 and CdCO3 crystals thus produced have interesting morphologies that are shown to arise because of interaction of the growing crystals with specific proteins secreted by the fungus during reaction. An additional advantage of this approach is that the reaction leads to detoxification of the aqueous solution and could have immense potential for bioremediation of heavy metals. Under conditions of this study, the metal ions are not toxic to the fungus, which readily grows after exposure to the metal ions. 相似文献
9.
Pinacol Formation and Reduction of Aromatic Carbonyls with Magnesium–Methanol at Ambient Temperature
Jitender M. Khurana Geeti Bansal Gagan Kukreja Ravi R. Pandey 《Monatshefte für Chemie / Chemical Monthly》2003,421(5):1365-1371
A simple and inexpensive procedure for the pinacol formation of aromatic aldehydes and reduction of aromatic ketones to the corresponding alcohols with magnesium in dry methanol at ambient temperature is reported. The pinacol formation and reduction are proposed to be proceeding by SET from magnesium. 相似文献
10.
A sensitive and inexpensive method of spectrophotometric determination of chromium(VI), based on the absorbance of its complex with malachite green and acetic acid at pH 2.5 is reported. The complex shows a molar absorptivity of 8 x 10(4) l.mole(-1) cm(-1) at 560 nm, using malachite green and acetic acid as reference solution. The effect of time, temperature, pH and reagent concentration is studied and optimum operating conditions are established. Beer's law is applicable in the concentration range 2.0-22.8 mug/ml chromium(VI). The resin beads act as a catalyst and as little as 1.6 mug of chromium(VI) is detected in the resin phase as compared to 4.1 mug in the solution phase. The standard deviation in the determinations is +/-0.40 mug/ml for a 10.35 mug/ml solution. 相似文献