全文获取类型
收费全文 | 2814篇 |
免费 | 329篇 |
国内免费 | 249篇 |
专业分类
化学 | 866篇 |
晶体学 | 4篇 |
力学 | 209篇 |
综合类 | 59篇 |
数学 | 1566篇 |
物理学 | 688篇 |
出版年
2024年 | 8篇 |
2023年 | 24篇 |
2022年 | 121篇 |
2021年 | 123篇 |
2020年 | 124篇 |
2019年 | 96篇 |
2018年 | 76篇 |
2017年 | 100篇 |
2016年 | 79篇 |
2015年 | 102篇 |
2014年 | 130篇 |
2013年 | 192篇 |
2012年 | 119篇 |
2011年 | 158篇 |
2010年 | 131篇 |
2009年 | 194篇 |
2008年 | 155篇 |
2007年 | 147篇 |
2006年 | 161篇 |
2005年 | 135篇 |
2004年 | 120篇 |
2003年 | 124篇 |
2002年 | 80篇 |
2001年 | 73篇 |
2000年 | 67篇 |
1999年 | 67篇 |
1998年 | 78篇 |
1997年 | 64篇 |
1996年 | 49篇 |
1995年 | 31篇 |
1994年 | 30篇 |
1993年 | 19篇 |
1992年 | 18篇 |
1991年 | 16篇 |
1990年 | 14篇 |
1989年 | 8篇 |
1988年 | 10篇 |
1985年 | 10篇 |
1984年 | 9篇 |
1983年 | 6篇 |
1982年 | 10篇 |
1981年 | 7篇 |
1980年 | 8篇 |
1979年 | 7篇 |
1978年 | 8篇 |
1977年 | 19篇 |
1976年 | 13篇 |
1975年 | 10篇 |
1974年 | 12篇 |
1973年 | 21篇 |
排序方式: 共有3392条查询结果,搜索用时 0 毫秒
41.
土壤环境中铅的化学 总被引:3,自引:0,他引:3
谢正苗 《广东微量元素科学》1996,3(11):24-28
论述了环境中铅的背景值、来源、污染、质量标准、化学循环以及环境中铅的烷基化,为铅污染治理提供理论依据。 相似文献
42.
The reaction between 1,4-pentadiyne and diethylaminotrimethylstannane leads predominantly to (E)-2-diethylamino-4-trimethylstannyl-2,4-pentaenyne (with either a 1/1 or 1/2 mol ratio of 1,4-pentadiyne and diethylaminotrimethylstannane). With 1/2 stoicheiometry 1,1,5-tris(trimethylstannyl)penta-1,2-dien-4-yne is formed as a minor product. 13C and 119Sn NMR data are reported. 相似文献
43.
Valery P. Nesterenko 《Journal of Thermal Analysis and Calorimetry》2005,80(3):575-577
Summary On the basis of calorimetric research of selenium dioxide, zirconium dioxide and zirconium diselenite dissolution reactions in the hydrofluoric acid solution under 298 K a standard enthalpy of Zr(SeO3)2 formation reaction from ZrO2 and SeO2 and a standard enthalpy of zirconium diselenite formation have been obtained. The value of enthalpy has been equal to -58.1±3.43 kJ mol-1 in ZrO2(solid)+2SeO2(solid) Zr(SeO3)2(solid) reaction. The standard enthalpy of zirconium diselenite formation is equal to Hf,2980Zr(SeO3)2(solid)= -1603.2±3.8 kJ mol-1. The Hf,2980 Zr(SeO3)2(solid) value has been determined for the first time. 相似文献
44.
Photo-extrusion of nitrogen from the azoalkane 1 in the presence of molecular oxygen gave besides the hydrocarbons 3 and 5, the endoperoxide 10 and hydroperoxide 11, the former via trapping of the 1,4-diradical 4 by triplet oxygen, the latter by ene-reaction-6f hydrocarbon 5 with singlet oxygen. 相似文献
45.
The reactions of Fe(CO)5, Fe(CO)4P(C6H5)3, M(CO)6 (M W, Mo, Cr), and (CH3C5H4Mn(CO)3 with KH and several boron and aluminium hydrides were investigated. Iron pentacarbonyl was converted quantitatively to K+Fe(CO)4-(CHO) by hydride transfer from KBH(OCH3)3 allowing isolation of [P(C6H5)3]2-Nn+Fe(CO)4(CHO)? in 50% yield. Lower yields were obtained with LiBH(C2H5)3, and other hydride sources gave little or no formyl product. The stability of Fe(CO)4(CHO)? in THP was found to depend on the cation, decreasing in the order [P(C6H5)3]2N+ > K+ > Na+ > Li+. No formyl complexes were isolated and no spectroscopic evidence for formyl formation was observed in the reactions of the other transition metal carbonyls with several hydride sources. Fe(CO)4-P(C6H5)3 gave K2Fe(CO)4 when treated with KHB(OCH3)3. When treated with LiBH(C2H5)3, W(CO)6 gave a mixture of HW2(CO)10?and (OC)5W(COC2H5)?; the latter was methylated to give the carbene complex (OC)5WC(OCH3)C2H5. 相似文献
46.
The Electron impact mass spectra of (CO)3 MC6H5—X complexes (M = Cr, W; X = OCH3, OC4H9, CO2CH3, CO2C4H9) were recorded. From metastable transitions and by high-resolution measurements complete fragmentation diagrams were obtained; in some cases comparative structure determinations of fragment ions were carried out by collisional activation. The fragmentation of the tungsten complexes considerably differs from that of the chromium compounds. The differences may be attributed to the stronger-electrophilic character as well as to the more pronounced tendency of tungsten to attain higher oxidation states. 相似文献
47.
Jing?Zhou Yuqi?Liu Liming?Tang Xinchen?Teng Ning?Tang Zhongxian?HuangEmail author 《中国科学B辑(英文版)》2003,46(1):64-74
Two mutants of the zinc finger protein, ZNF191 (243–368) I323W and R327W, are successfully obtained by site-directed mutagenesis.
The fluorescence spectrum is used to study the interaction between these two mutants and the oligonucleotides. The influence
of the mutation on the interaction has been studied using ethidium bromide (EB) as the fluorescence probe. The binding constants
of the I323W-DNA and R327W-DNA have been calculated and the possible binding models have been discussed. 相似文献
48.
Optimal design and operation of bioreactors for insect cell culture is facilitated by functional relations providing quantitative
information on cellular metabolite consumption kinetics, as well as on the specific cell growth rates (μG). Initial specific consumption rates of glucose, malate, and oxygen, and associated changes in μG, were measured forSpodoptera frugiperda clone 9 (Sf9) cells grown in batch suspension culture in medium containing 7–35 mM glucose, 0–16 mM malate, and 4–16 mM glutamine.
The initial specific glucose consumption rate (q
G
) could be described by a modified Michaelis-Menten equation treating malate as a “competitive” inhibitorK
1 = 6.5 mM) and glutamine as a “noncompetitive” inhibitorK
I
= 14 mM) ofq
G
, with aK
m
of 7.1 mM for glucose. All three carbon sources were found to increase μG in a saturable manner, and a modified Monod equation was employed to describe this relationship (μGmax = 0.047 h-1). The initial specific oxygen consumption rate (qO2) in Sf9 cells could be related to μG by the maintenance energy model, and it was calculated that, under typical culture conditions, about 15–20% of the cellular
energy demand comes from functions not related to growth. Fitted parameters in mathematical expression for μg: K4, Monod constant for glucose (mM); K5, modified Monod constant for malate (mM); K6, Monod constant for glutamine (mM); mo2, specific consumption rate of oxygen by the cells under zero-growth conditions (nmol/cell/h); qF, initial specific fumarate production rate (nmol/cell/ h);q
G
, initial specific glucose consumption rate (nmol/cell/h); qGmax, maximum initial specific glucose consumption rate (nmol/cell/h);q
M
, initial specific malate consumption rate (nmol/cell/h); qo2, initial specific oxygen consumption rate (nmol/cell/h); Yo2, cell yield on oxygen (cells/nmol); μ, initial specific cell growth rate (h-1); μg, initial specific cell growth rate (h-1); μGmax, maximum initial specific cell growth rate (h-1). 相似文献
49.
50.
The fast trace analysis method used to monitor 2,3,7,8-TCDD in stack gas during the incineration of the waste from Seveso is described. The sampling of volatile organic compounds from flue gases, distributed between all three aggregation states, is based on a micromethod developed for the trace analysis of water using a specially dimensioned adsorptive charcoal filter (1.5 mg charcoal). In conjunction with subsequent GC/MS measurements the rapid “fast cycle trace analysis” ensured specific 2,3,7,8-TCDD detection down to 100 pg per m3 flue gas in cycle times of about 1–2 hours. 相似文献