首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   5000篇
  免费   120篇
  国内免费   19篇
化学   3501篇
晶体学   45篇
力学   113篇
数学   668篇
物理学   812篇
  2024年   18篇
  2023年   39篇
  2022年   90篇
  2021年   129篇
  2020年   110篇
  2019年   92篇
  2018年   66篇
  2017年   69篇
  2016年   188篇
  2015年   117篇
  2014年   138篇
  2013年   301篇
  2012年   359篇
  2011年   394篇
  2010年   218篇
  2009年   182篇
  2008年   331篇
  2007年   325篇
  2006年   261篇
  2005年   307篇
  2004年   233篇
  2003年   204篇
  2002年   169篇
  2001年   68篇
  2000年   66篇
  1999年   38篇
  1998年   45篇
  1997年   35篇
  1996年   70篇
  1995年   32篇
  1994年   35篇
  1993年   43篇
  1992年   27篇
  1991年   30篇
  1990年   37篇
  1989年   27篇
  1988年   27篇
  1987年   34篇
  1986年   17篇
  1985年   30篇
  1984年   21篇
  1983年   13篇
  1982年   17篇
  1981年   13篇
  1980年   14篇
  1979年   14篇
  1978年   10篇
  1977年   8篇
  1974年   6篇
  1972年   3篇
排序方式: 共有5139条查询结果,搜索用时 15 毫秒
51.
Reaction of N-(4-pyridylmethyl)benzamide N-oxides 2a-f with ethyl cyanoacetate in the presence of acetic anhydride yield dimerization compounds 3a-f and (E)-ethyl 2-cyano-3-(4-pyridyl)-3(benzoylamino)acrylates 4a-f , which react with hydrazine to give 4-cyano-3-(4-pyridyl)-3-pyrazolin-5-one 9 and the corresponding benzamides 10a-f .  相似文献   
52.
Cellulose nanocrystals (CNCs) spontaneously assemble into gels when mixed with a polyionic organic or inorganic salt. Here, we have used this ion-induced gelation strategy to create functional CNC gels with a rigid tetracationic macrocycle, cyclobis(paraquat-p-phenylene) ( CBPQT 4+). Addition of [ CBPQT ]Cl4 to CNCs causes gelation and embeds an active host inside the material. The fabricated CNC gels can reversibly absorb guest molecules from solution then undergo molecular recognition processes that create colorful host–guest complexes. These materials have been implemented in gel chromatography (for guest exchange and separation), and as elements to encode 2- and 3-dimensional patterns. We anticipate that this concept might be extended to design a set of responsive and selective gel-like materials functioning as, for instance, water-pollutant scavengers, substrates for chiral separations, or molecular flasks.  相似文献   
53.
Summary The kinetics of the anation reaction of [Co(NH3)5H2O]3+ by H3PO3/H2PO 3 , to give [CoH2PO3(NH3)5]2+, have been studied at 60, 70 and 80°C, in the acidity range [H+](M)=1.5 · 10–1 –2.0 · 10–3. Only H2PO3 is found to be reactive. The rate data is consistent with an Id mechanism. The mean value of outer sphere association of [Co(NH3)H2O]3+ with H2PO 3 is 1.5 M–1. Values of the interchange constants are: 1044ki(s–1)= 0.29, 1.47, 5.13, at 60, 70 and 80 °C respectively (H= 1.4 · 102KJmol–1, S=8.3 · 10 JK–1 mol–1). The first acidity constant of H3PO3 at I=1.0 has also been determined: 102Ka(M)=4.8, 5.2 and 5.5, at 25, 40 and 50 °C respectively.  相似文献   
54.
The enhancement of the activity of a carbon treated with HF is due to the drastic diminution of its inorganic impurities, which produces an increase of the surface area of the carbon, a stronger Pt-C interaction and a higher Pt dispersity.
, HF, , , Pt-C Pt.
  相似文献   
55.
Carbon-carbon sp3-sp2 rotational barriers of 3,3-dimethyl-2-(3,4,5-trimethoxyphenyl)-4-piperidones and their ethylene ketals have been evaluated using nmr techniques. The conformation of 1 hydrochloride has been studied by NOE determinations. Values found for the hydrochlorides of the title compounds are discussed in terms of equilibria with free bases and nitrogen inversion.  相似文献   
56.
A photoelectrochemical cell for hydrogen peroxide production using flavin photosystems is described. The anodic solution, which is kept free of oxygen by passing an Ar stream through it, contains the photoreceptor (flavin mononucleotide or lumiflavin) and the electron donor (EDTA, semicarbazide or hydroxylamine), while the peroxide is formed at the electrode of the cathodic solution, whose oxygen content is increased by bubbling with pure oxygen. Among several electrode metals that have been tested (Ag, Pt and Hg), Hg is the most efficient. The pH of the anodic and cathodic solutions should be adjusted to 14 and 1, respectively, for optimum results.  相似文献   
57.
    
Metallacarboranes with the shape of the Greek letter θ, such as [Co(C2B9H11)2], were tested, for the first time, as efficient photoredox catalysts in the oxidation of aromatic and aliphatic alcohols in water. Their efficiency is linked to their high solubility in water, their high oxidizing power (Co4+/3+), and their absence of fluorescence on excitation, among others. In most of the studied examples, using a catalyst load of 0.4 mol % gave high yields of 90–95 % with selectivity greater than 99 %. By reducing the catalyst load to 0.01 mol %, quantitative conversion of reactants to products was achieved, in some cases with greater than 99 % yield, high catalyst efficiency reaching a turnover number of 10 000, and a higher yield with a 45 times lower concentration of catalyst. The metallacarboranes can be recovered easily by precipitation on addition of [NMe4]Cl. A pathway for the photoredox-catalyzed oxidation of alcohols is proposed.  相似文献   
58.
    
The site-selective modification of biomolecules has grown spectacularly in recent years. The presence of a large number of functional groups in a biomolecule makes its chemo- and regioselective modification a challenging goal. In this context, transition-metal-mediated reactions are emerging as a powerful tool owing to their unique reactivity and good functional group compatibility, allowing highly efficient and selective bioconjugation reactions that operate under mild conditions. This Minireview focuses on the current state of organometallic chemistry for bioconjugation, highlighting the potential of transition metals for the development of chemoselective and site-specific methods for functionalization of peptides, proteins and nucleic acids. The importance of the selection of ligands attached to the transition metal for conferring the desired chemoselectivity will be highlighted.  相似文献   
59.
    
An original method for determining the handedness of individual non-centrosymmetric crystals in a mixture using a tightly-focused, circularly polarized X-ray beam is presented. The X-ray natural circular dichroism (XNCD) spectra recorded at the metal K-edge on selected crystals of [Δ-M(en)3](NO3)2 and [Λ-M(en)3](NO3)2 (M=CoII, NiII) show extrema at the metal pre-edge (7712 eV for Co, 8335 eV for Ni). A mapping of a collection of some 220 crystals was performed at the respective energies by using left and right circular polarizations. The difference in absorption for the two polarizations, being either negative or positive, directly yielded the handedness of the crystal volume probed by the beam. By using this technique, it was found that the addition of l -ascorbic acid during the synthesis of [Co(en)3](NO3)2 resulted in an enantiomeric enrichment of the Λ-isomer of 67±13 %, whereas the Ni analogue was similarly, but conversely, enriched in the Δ-isomer (65±22 %).  相似文献   
60.
    
The light-gated organocatalysis via the release of 4-N,N-dimethylaminopyridine (DMAP) by irradiation of the [Ru(bpy)2(DMAP)2]2+ complex with visible light was investigated. As model reaction the acetylation of benzyl alcohols with acetic anhydride was chosen. The pre-catalyst releases one DMAP molecule on irradiation at wavelengths longer than 455 nm. The photochemical process was characterized by steady-state irradiation and ultrafast transient absorption spectroscopy. The latter enabled the observation of the 3MLCT state and the spectral features of the penta-coordinated intermediate [Ru(bpy)2(DMAP)]2+. The released DMAP catalyzes the acetylation of a wide range of benzyl alcohols with chemical yields of up to 99 %. Control experiments revealed unequivocally that it is the released DMAP which takes the role of the catalyst.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号