全文获取类型
收费全文 | 2260篇 |
免费 | 93篇 |
国内免费 | 7篇 |
专业分类
化学 | 1607篇 |
晶体学 | 25篇 |
力学 | 57篇 |
数学 | 319篇 |
物理学 | 352篇 |
出版年
2022年 | 14篇 |
2021年 | 25篇 |
2020年 | 21篇 |
2019年 | 24篇 |
2018年 | 21篇 |
2017年 | 10篇 |
2016年 | 53篇 |
2015年 | 50篇 |
2014年 | 61篇 |
2013年 | 146篇 |
2012年 | 115篇 |
2011年 | 142篇 |
2010年 | 88篇 |
2009年 | 68篇 |
2008年 | 121篇 |
2007年 | 123篇 |
2006年 | 138篇 |
2005年 | 119篇 |
2004年 | 127篇 |
2003年 | 96篇 |
2002年 | 86篇 |
2001年 | 22篇 |
2000年 | 28篇 |
1999年 | 23篇 |
1998年 | 26篇 |
1997年 | 28篇 |
1996年 | 34篇 |
1995年 | 25篇 |
1994年 | 27篇 |
1993年 | 25篇 |
1992年 | 17篇 |
1991年 | 19篇 |
1990年 | 18篇 |
1989年 | 26篇 |
1988年 | 21篇 |
1987年 | 13篇 |
1986年 | 20篇 |
1985年 | 34篇 |
1984年 | 33篇 |
1983年 | 23篇 |
1982年 | 22篇 |
1981年 | 28篇 |
1980年 | 31篇 |
1979年 | 20篇 |
1978年 | 17篇 |
1977年 | 23篇 |
1976年 | 15篇 |
1975年 | 21篇 |
1974年 | 12篇 |
1973年 | 20篇 |
排序方式: 共有2360条查询结果,搜索用时 15 毫秒
991.
Novel illustrations of the specific reactivity of 1,1-diamino-2,2-dinitroethene (DADNE) leading to new unexpected compounds 总被引:2,自引:0,他引:2
1,1-Diamino-2,2-dinitroethene (DADNE) was further investigated and evaluated in oxidation and azidation reactions. DADNE gave new unexpected products as a result of its specific reactivity as previously observed. The X-ray structure determination was the key of success in this work enabling us to perfectly characterise the new products and argue about the reaction mechanisms as well. Once again, the nucleophilic gem-dinitrocarbon of DADNE seemed to be directly involved in these transformations. Attempts to change the regioselectivity were performed by modifying the experimental conditions. 相似文献
992.
The reaction products in the SF6-N2 mixture rf plasma during reactive ion etching of Si and W have been measured by a mass spectrometric method. Two kinds of cathode materials were used in this work; they were stainless steel for the Si etching, and SiO2 for the W etching. The main products detected in the etching experiments of Si and W included SF4, SF2, SO2, SOF2, SOF4, SO2F2, NSF, NF3, N2F4, NxSy, NO2, and SiF4. In the W etching with the SiO2 cathode, additional S2F2, N2O, and WF6 molecules were also obtained. The formation reactions about the novel NSF compound and the sulfur oxyfuorides were discussed. 相似文献
993.
994.
Influence of operating conditions on the retention of phosphate in water by nanofiltration 总被引:1,自引:0,他引:1
The objective of this study was to investigate the retention of phosphate anions, H2PO4− and HPO42−, by nanofiltration. The first part of this study deals with the characterisation of the NF200 membrane used in permeation experiments with aqueous solutions of neutral organic and charged inorganic solutes. In the second part the effects of feed pressure, ionic strength, concentration and pH on the retention of phosphate anions were investigated. Results show that the membrane is negatively charged, its pore radius is around 0.5 nm and the retention order for the salts tested was R(Na2SO4) > R(NaCl) > R(CaCl2). The retentions of phosphate anions are in the order of 85% for H2PO4− and 96% for HPO42−. They are relatively high when compared to retentions of other anions with the same charge. The retentions of phosphate anions, particularly the monovalent species, depend on the chemical parameters (feed concentration, ionic strength, and pH) and applied pressure. The experimental data were analysed using the Speigler–Kedem model and the transport parameters, i.e., the reflection coefficient (σ) and solute permeability (Ps) have been determined. 相似文献
995.
John R. Tate Katherine Kantardjieff Guy Crundwell Larry M. Mink 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(9):m485-m486
In the title compound, [PtBr2(C48H36N4O4)]·0.896CHCl3·0.569CH3CN, the centrosymmetric metal complex is octahedral, with the porphyrin ring essentially planar and the Br atoms occupying axial positions. The two independent methoxyphenyl substituents are tilted at angles of 89.0 and 67.0° with respect to the porphyrin plane. The Pt—N distances are 2.035 (4) and 2.036 (4) Å and the Pt—Br distance is 2.4666 (6) Å. Chloroform and acetonitrile solvent molecules, exhibiting substantial disorder, occupy positions between the porphyrin molecules. This is the first crystal and molecular structure of a PtIV–porphyrin complex to be reported. 相似文献
996.
The proton affinities of 2(5H)-furanone, 1 (836 kJ/mol), 5,6-dihydro-2H-pyran-2-one, 2 (862 kJ/mol), cyclopentenone, 3 (857 kJ/mol), and cyclohexenone, 4 (863 kJ/mol), have been measured by Fourier transform ion cyclotron resonance techniques. A comparison is made with (reexamined) data concerning saturated cyclic and unsaturated aliphatic analogs. Three general observations are made. First, the basicity is found to increase with the size of the ring. Second, unsaturated lactones are more basic than their corresponding aliphatic unsaturated esters. Third, unsaturated and saturated lactones have almost identical gas-phase basicities, while unsaturated and saturated lactones have almost identical gas-phase basicities, while unsaturated cyclic ketones are more basic than their saturated analogs. All these experimental findings have been rationalized by means of ab initio calculations up to the G2(MP2,SVP) level. The basicity trends along the series are the result of two main factors: the different hybridization pattern of the carbonyl carbon as the size of the ring changes and, in the case of lactones, the nonbonding interaction between the proton attached to the carbonyl group and the ether-like oxygen which contributes to the enhanced stability of the protonated form. For unsaturated ketones the C=C double bond participates fully in the change in charge distribution induced by the protonation, while for unsaturated lactones the existence of an oxygen atom within the ring impedes this shift of the electron density. 相似文献
997.
He H Janso JE Williamson RT Yang HY Carter GT 《The Journal of organic chemistry》2003,68(16):6079-6082
Cytosporacin (1), a novel antibacterial polyketide containing naphthopyranone and isochromandione moieties, was isolated from the fermentation broth of the fungus Cytospora rhizophorae. A (1)H-detected ACCORD-ADEQUATE pulse sequence that distinguished (2)J(CH) from (3)J(CH) correlations provided critical information for structural determination. NOE studies established the relative configuration and revealed the presence of two rotamers. A biosynthetic (13)C-labeling experiment indicated that cytosporacin was derived from acetate origin. 相似文献
998.
999.
George R. De Maré Hélène Deslauriers Guy J. Collin 《Research on Chemical Intermediates》1990,14(2):133-159
The 184.9 nm photochemistry 0f gaseous 3-methylcyclopentene and 3-methyl-1,4-pentadiene have been studied. Both photoexcited
species decompose mainly through the primayy rupture of the C-CH3 bond. Vibrationally excited 3-cyclopenennyl and pentamethylene radicals are formed in the primayy decomposition in the former
and latter systems respectively. These radicals are connected through isomerization reactions: in the presence of DI, the
isomers cyclopenten,, and trans-1,3-pentadtene and/or vinylcyclopropane are formed in both systems. The quantum yields depend
on the pressure and the starting monomer: cyclopentene and cyclopentadiene are the major products from the photolysis of 3-methylcyclopentene
+ DI mixtures and only minor quantities of the other C5H8 compounds are formed. Cyclopentadiene is the major product of the photolysis of 3-methyl-1,4-pentadiene + O2 mixtures whereas vinylcyclopropane and trans-1,3-pentadiene are the major C5 producss of the photolysis of 3-methyl-1,4-pentadiene + DI mixtures.
The geometries of 3-cyclopentenyl and of the structures at the six critical points in the torsional potential energy curve
(TPEC) for rotation about the 2- and 3-C-C bonds in the open chain pentamethylene species have been optimized completely by
ab initio RHF-SCF gradient methods. For the open-chain structures the bond orders, bond lengths and the free valence (primarily
associated with the central carbon atom) all correspond to 1,4-pentadien-3-yl conformations. In the ground state there is
a high barrier to formation of 3-cyclopentenyl from 1,4-pentadien-3-yl. The features (relative energies and torsionll barriers)
of the TPEC for 1,4-pentadien-3-yl explain the ESR observations for the open chain C5H7 radical rotamers. 相似文献
1000.
From calorimetric measurements a model of solution is proposed for LiAlH4 in THF. It is ionised as LiAlH4 ? Li+ + AlH?4. For this reaction, ΔHi = 3.05 kcal mol?1 and the dissociation constant is K = 0.11. 相似文献