全文获取类型
收费全文 | 6643篇 |
免费 | 625篇 |
国内免费 | 411篇 |
专业分类
化学 | 4246篇 |
晶体学 | 85篇 |
力学 | 275篇 |
综合类 | 29篇 |
数学 | 1398篇 |
物理学 | 1646篇 |
出版年
2023年 | 109篇 |
2022年 | 141篇 |
2021年 | 230篇 |
2020年 | 246篇 |
2019年 | 306篇 |
2018年 | 276篇 |
2017年 | 230篇 |
2016年 | 320篇 |
2015年 | 283篇 |
2014年 | 358篇 |
2013年 | 529篇 |
2012年 | 526篇 |
2011年 | 506篇 |
2010年 | 331篇 |
2009年 | 344篇 |
2008年 | 397篇 |
2007年 | 327篇 |
2006年 | 265篇 |
2005年 | 208篇 |
2004年 | 200篇 |
2003年 | 161篇 |
2002年 | 159篇 |
2001年 | 130篇 |
2000年 | 104篇 |
1999年 | 64篇 |
1998年 | 47篇 |
1997年 | 45篇 |
1996年 | 59篇 |
1995年 | 46篇 |
1994年 | 41篇 |
1993年 | 50篇 |
1992年 | 44篇 |
1991年 | 44篇 |
1990年 | 38篇 |
1989年 | 27篇 |
1988年 | 29篇 |
1987年 | 44篇 |
1986年 | 40篇 |
1985年 | 37篇 |
1984年 | 30篇 |
1983年 | 29篇 |
1982年 | 33篇 |
1981年 | 31篇 |
1980年 | 23篇 |
1979年 | 38篇 |
1978年 | 26篇 |
1977年 | 23篇 |
1976年 | 27篇 |
1975年 | 20篇 |
1974年 | 14篇 |
排序方式: 共有7679条查询结果,搜索用时 76 毫秒
101.
钯镁基体改进剂对铅,铋,锗在石墨炉中原子化影响的研究 总被引:7,自引:0,他引:7
通过原子吸收和X-射线衍射分析证明,加入钯镁基体改进剂在预热处理后对Pb、Bi和Ge三个元素分别生成金属间化合物PbPd_3、BiPd_3、Ge_9Pd_(23)和其他化合物,从而提高了最高允许灰化温度,改变了原子化机理。在原子化阶段这些金属间化合物直接分解为金属原子,结果提高测定灵敏度。 相似文献
102.
Yinghong Sheng Jerzy Leszczynski Thuc-Quyen Nguyen Anu Bamgbelu 《Structural chemistry》2007,18(6):827-832
A theoretical study using density functional theory was performed to understand the structure/property relationship of the
cationic conjugated polyelectrolytes, poly[9,9-bis-(6′-N,N,N-trimethylammonium) hexyl] fluorene-alt-4,7-(2,1,3-benzothiadiazole)] (PFBT-X, where X = Br). The torsion angle between the fluorene and benzothiadiazole units in the PFBT monomer was found to substantially affect
the structural and electronic properties of the cationic PFBT monomer. The changes of geometrical parameter, HOMO and LUMO energy levels, and band gap, as well as the absorption maximum
are discussed in terms of the torsion in the PFBT monomer structure. For comparison, its neutral analogue, the monomer of
poly(9,9-di-n-octylfluorene-alt-benzothiadiazole) (F8BT) was also studied. The length of conjugation backbone was also examined. 相似文献
103.
Hu C Chin RM Nguyen TD Nguyen KT Wagenknecht PS Nathan LC 《Inorganic chemistry》2003,42(23):7602-7607
The reactions between H(2)dc3 and Co(acac)(3) have been studied in the presence and absence of base. In the presence of base, a complex with an intramolecular Co-C bond, Co(dc3-C-(8))(H(2)O), 1, is formed, presumably through heterolytic C-H bond activation. An X-ray crystallographic study demonstrates the presence of a Co-C bond and shows that the diazacyclooctane (daco) subunit adopts the chair-boat conformation with respect to the metal. The cobalt-carbon bond induces strain in the macrocycle as demonstrated by bond angles significantly deviating from tetrahedral. The (13)C NMR resonance of the carbon atom bound to cobalt (-10.5 ppm) suggests significant ionic character in the cobalt-carbon bond. However, we were unable to cleave this bond in the presence of strong acid. In the absence of base, the reaction of Co(acac)(3) with H(2)dc3 resulted in C-N cleavage of the ligand and the formation of a complex of dioxocyclam, Co(dc)(acac), 2. This complex has subsequently been prepared in high yield by the reaction of Co(acac)(3) with dioxocyclam. An X-ray crystallographic study demonstrates that dioxocyclam adopts the heretofore unreported cis configuration, having folded along a N-Co-N axis that is perpendicular to the Co-acac plane. 相似文献
104.
105.
ABSTRACTThis study proposes a simple method of designing a high-speed liquid crystal variable retarder (LCVR) with reflection mode. First, a series of simple formulas is provided for analysing the effects of tilt incidence and birefringence of the liquid crystal on the phase retardation and response time of the LCVR. Then, a reflective LCVR is fabricated to validate the theoretical analysis. Measured results show that the response speed can reach 2.7 kHz with a phase retardation of 1 λ. Furthermore, the theoretical curve is close to the measured curve while the incident angle is less than 10°. However, the theoretical and measured values show a considerable difference under a large incident angle. This problem is discussed, and a modified method is given. This work is helpful for the design and fabrication of high-speed LCVR. 相似文献
106.
Nguyen Chan Hung I. V. Anoshkin E. G. Rakov 《Russian Journal of Applied Chemistry》2007,80(3):443-447
Method of thermodynamic simulation was used to calculate the equilibrium parameters of reactions of graphite with anhydrous LiOH, NaOH, and KOH and with the alkalis in the presence of water vapor. The change in the specific surface area and mass loss were used to analyze the interaction of carbon nanofibers and multilayer carbon nanotubes produced by catalytic pyrolysis of CH4 with the alkalis. 相似文献
107.
Bose G Nguyen VT Ullah E Lahiri S Görls H Langer P 《The Journal of organic chemistry》2004,69(26):9128-9134
The Lewis acid mediated domino "[3+3]-cyclization-homo-Michael" reaction of 1,3-bissilyl enol ethers with 1,1-diacylcyclopropanes allows an efficient one-pot synthesis of functionalized salicylates containing a halogenated side chain. A great variety of substitution patterns could be realized by variation of the starting materials and of the Lewis acid. The mechanism of the domino process was studied. 相似文献
108.
Grignard reactions with alkoxysilanes or carbonyl compounds produce alkoxymagnesium halides as by-products. Kinetic measurements for reactions of silanes and of a ketone were performed with Grignard reagents, enriched in alkoxymagnesium halides and taken in a great excess.The alkoxide-type reaction products complex tightly with Grignard reagents and enhance in this way their nucleophilicity, thus accelerating the reaction. However, alkoxides branched at α-C atom exert an unfavorable steric hindrance to reaction resulting in a decrease in the reaction rate. 相似文献
109.
The synthesis of model long-chain hydrocarbons (C13 and C19) carrying a vinyl group and a trichloro- or a triethoxysilyl group at each end is reported. These compounds are suitable for linkage to a hydroxylated silicon surface and at the other end with vinyl group for further functionalization and multilayer formation. 相似文献
110.
Hong-Jie ZhangGhee Teng Tan Vu Dinh HoangNguyen Van Hung Nguyen Manh CuongDjaja Doel Soejarto John M PezzutoHarry H.S Fong 《Tetrahedron》2003,59(2):141-148
Bioassay directed-fractionation led to the identification of litseaverticillols A-H (1-8) from the leaves and twigs of Litsea verticillata Hance. These new sesquiterpenes possess a unique skeleton that was recently designated as ‘litseane’. The structures of these compounds were determined by spectroscopic means including 1D and 2D NMR data. Structural configurations were determined by ROESY experiments. Mosher ester reactions and optical rotation measurements established the sesquiterpenes 1-8 as racemates. Isolates 1-8 inhibited HIV-1 replication in HOG.R5 cells with IC50 values ranging from 2 to 15 μg/ml (8-58 μM) while affecting the growth of HOG.R5 at concentrations 2-3-fold higher. Based on this data, structure-activity relationships can be discerned, suggesting compounds of this class are good candidates for analog production. 相似文献