全文获取类型
收费全文 | 3090篇 |
免费 | 131篇 |
国内免费 | 11篇 |
专业分类
化学 | 1937篇 |
晶体学 | 32篇 |
力学 | 95篇 |
数学 | 532篇 |
物理学 | 636篇 |
出版年
2023年 | 31篇 |
2022年 | 43篇 |
2021年 | 46篇 |
2020年 | 64篇 |
2019年 | 55篇 |
2018年 | 39篇 |
2017年 | 30篇 |
2016年 | 96篇 |
2015年 | 102篇 |
2014年 | 95篇 |
2013年 | 161篇 |
2012年 | 167篇 |
2011年 | 219篇 |
2010年 | 120篇 |
2009年 | 85篇 |
2008年 | 148篇 |
2007年 | 148篇 |
2006年 | 135篇 |
2005年 | 100篇 |
2004年 | 90篇 |
2003年 | 80篇 |
2002年 | 76篇 |
2001年 | 40篇 |
2000年 | 38篇 |
1999年 | 31篇 |
1998年 | 37篇 |
1997年 | 37篇 |
1996年 | 44篇 |
1995年 | 62篇 |
1994年 | 41篇 |
1993年 | 41篇 |
1992年 | 35篇 |
1991年 | 33篇 |
1990年 | 28篇 |
1989年 | 26篇 |
1988年 | 41篇 |
1987年 | 39篇 |
1986年 | 29篇 |
1985年 | 40篇 |
1984年 | 42篇 |
1983年 | 23篇 |
1982年 | 31篇 |
1981年 | 31篇 |
1979年 | 29篇 |
1978年 | 26篇 |
1976年 | 21篇 |
1975年 | 22篇 |
1974年 | 17篇 |
1973年 | 27篇 |
1972年 | 17篇 |
排序方式: 共有3232条查询结果,搜索用时 15 毫秒
101.
Peter Brenneisen Jinsook Oh Meinhard Wlaschek Jutta Wenk Karlis Briviba Christina Hommel Gemot Herrmann Helmut Sies Karin Scharffetter-Kochanek 《Photochemistry and photobiology》1996,64(5):877-885
Abstract— The wavelength dependence for the regulation of two major matrix-metalloproteinases, interstitial collagenase (MMP-1) and stromelysin-1 (MMP-3), and their major inhibitor, tissue inhibitor of metalloproteinases (TIMP-1), was studied in human dermal fibroblasts in vitro. Monochromatic irradiation at 302, 307, 312 and 317 nm with intensities ranging from 20 to 300 J/m2 increased MMP-1 and MMP-3 mRNA steady-state levels and the secretion of the corresponding proteins up to 4.4-fold, whereas almost no increase was observed at wavelengths <290 nm. In contrast, the synthesis of TIMP-1 increased only marginally. This unbalance may contribute to the severe connective tissue damage related to photoaging of the skin. The wavelengths responsible for MMP-1 and MMP-3 induction reported here are distinct from the absorption spectrum of DNA and are different from results previously reported in the literature. Importantly, they overlap with wavelengths whose intensity is predicted to increase on the earth's surface upon ozone depletion. Intensities and particular wavelengths used in our studies in vitro can be absorbed readily by fibroblasts within the skin in vivo and, thus, are relevant for risk assessment and development of protective agents. 相似文献
102.
Bruggink C Maurer R Herrmann H Cavalli S Hoefler F 《Journal of chromatography. A》2005,1085(1):104-109
A versatile liquid chromatographic platform has been developed for analysing underivatized carbohydrates using high performance anion exchange chromatography (HPAEC) followed by an inert PEEK splitter that splits the effluent to the integrated pulsed amperometric detector (IPAD) and to an on-line single quadrupole mass spectrometer (MS). Common eluents for HPAEC such as sodium hydroxide and sodium acetate are beneficial for the amperometric detection but not compatible with electrospray ionisation (ESI). Therefore a membrane-desalting device was installed after the splitter and prior to the ESI interface converting sodium hydroxide into water and sodium acetate into acetic acid. To enhance the sensitivity for the MS detection, 0.5 mmol/l lithium chloride was added after the membrane desalter to form lithium adducts of the carbohydrates. To compare sensitivity of IPAD and MS detection glucose, fructose, and sucrose were used as analytes. A calibration with external standards from 2.5 to 1000 pmole was performed showing a linear range over three orders of magnitude. Minimum detection limits (MDL) with IPAD were determined at 5 pmole levels for glucose to be 0.12 pmole, fructose 0.22 pmole and sucrose 0.11 pmole. With MS detection in the selected ion mode (SIM) the lithium adducts of the carbohydrates were detected obtaining MDL's for glucose of 1.49 pmole, fructose 1.19 pmole, and sucrose 0.36 pmole showing that under these conditions IPAD is 3-10 times more sensitive for those carbohydrates. The applicability of the method was demonstrated analysing carbohydrates in real world samples such as chicory inulin where polyfructans up to a molecular mass of 7000 g/mol were detected as quadrupoly charged lithium adducts. Furthermore mono-, di-, tri-, and oligosaccharides were detected in chicory coffee, honey and beer samples. 相似文献
103.
Jean-Franjois Nierengarten Andreas Herrmann Rik R. Tykwinski Markus Riittimann Francois Diederich Corinne Boudon Jean-Paul Gisselbrecht Maurice Gross 《Helvetica chimica acta》1997,80(1):293-316
The synthesis of (E)-hex-3-ene-l, 5-diynes and 3-methylidenepenta-1, 4-diynes with pendant methano[60]-fullerene moieties as precursors to C60-substituted poly(triacetylenes) (PTAs, Fig. 1) and expanded radialenes (Fig. 2) is described. The Bingel reaction of diethyl (E)-2, 3-dialkynylbut-2-ene-1, 4-diyl bis(2-bromopropane-dioates) 5 and 6 with two C60 molecules (Scheme 2) afforded the monomeric, silyl-protected PTA precursors 9 and 10 which, however, could not be effectively desilylated (Scheme 4). Also formed during the synthesis of 9 and 10 , as well as during the reaction of C60 with thedesilylated analogue 16 (Scheme 5 ), were the macrocyclic products 11, 12 , and 17 , respectively, resulting from double Bingel addition to one C-sphere. Rigorous analysis revealed that this novel macrocyclization reaction proceeds with complete regio- and diastereoselectivity. The second approach to a suitable PTA monomer attempted N, N′-dicyclohexylcarbodiimide(DCC)-mediated esterification of (E)-2, 3-diethynylbut-2-ene-l, 4-diol ( 18 , Scheme 6) with mono-esterified methanofullerene-dicarboxylic acid 23 ; however, this synthesis yielded only the corresponding decarboxylated methanofullerene-carboxylic ester 27 (Scheme 7). To prevent decarboxylation, a spacer was inserted between the reacting carboxylic-acid moiety and the methane C-atom in carboxymethyl ethyl 1, 2-methano[60]fullerene-61, 61-dicarboxylate ( 28 , Scheme 8), and DCC-mediated esterification with diol 18 afforded PTA monomer 32 in good yield. The formation of a suitable monomeric precursor 38 to C60-substituted expanded radialenes was achieved in 5 steps starting from dihydroxyacetone (Schemes 9 and 10), with the final step consisting of the DCC-mediated esterification of 28 with 2-[1-ethynyl(prop-2-ynylidene)]propane-1, 3-diol ( 33 ). The first mixed C60-C70 fullerene derivative 49 , consisting of two methano[60]fullerenes attached to a methano[70]fullerene, was also prepared and fully characterized (Scheme 13). The Cs-symmetrical hybrid compound was obtained by DCC-mediated esterification of bis[2-(2-hydroxy-ethoxy)ethyl] 1, 2-methano[70]fullerene-71, 71-dicarboxylate ( 46 ) with an excess of the C60-carboxylic acid 28 . The presence of two different fullerenes in the same molecule was reflected by its UV/VIS spectrum, which displayed the characteristic absorption bands of both the C70 and C60 mono-adducts, but at the same time indicated no electronic interaction between the different fullerene moieties. Cyclic voltammetry showed two reversible reduction steps for 49 , and comparison with the corresponding C70 and C60 mono-adducts 46 and 30 indicated that the three fullerenes in the composite fullerene compound behave as independent redox centers. 相似文献
104.
Salter L Clifford T Morley N Gould D Campbell S Curnow A 《Journal of photochemistry and photobiology. B, Biology》2004,75(1-2):57-61
Comet assay data (tail DNA %) have been gathered for the concentration dependent role of three antioxidants (AOs); quercetin (Q), epigallocatechin gallate (EGCG) and N-acetylcysteine (NAC) in reducing UV-induced damage to DNA in normal fetal lung fibroblasts (MRC5). All three compounds demonstrate a concentration dependent reduction maximum with a pro-oxidant effect at higher (though not cytotoxic) concentrations. Manipulation of a simple 4-step reaction mechanism for free radical (FR) scavenging by AOs produced rate constant ratios which allowed the relative effectiveness (Q > EGCG > NAC) of the AOs to be evaluated. 相似文献
105.
H. Herrmann H.-W Jacobi G. Raabe A. Reese R. Zellner 《Fresenius' Journal of Analytical Chemistry》1996,355(3-4):343-344
Nitrate radical (NO3) reactions with benzene (R-1), toluene (R-2), p-xylene (R-3), p-cresol (R-4) and mesitylene (R-5) have been studied by laser photolysis/long path laser absorption (LP-LPLA) in aqueous solution. Rate constants of k1=(4.0±0.6) 108, k2=(1.2±0.3)109, k3=(1.6±0.1)109, k4= (8.4±2.3)108 and k5=(1.3±0.3)109 lmol-1s-1 were obtained at T=298 K. In addition, reaction rate coefficients for SO-5+Fe2+prod. (R-6) and SO-5+Mn2+prod. (R-7) of k6=(4.3±2.4) 107 lmol-1s-1 and k7=(4.6±1.0)106 lmol-1s-1 (T=298 K, I0) have been obtained by the application of laser photolysis/UV-VIS broadband diode array spectroscopy. A new laser photolysis/UV-long path laser absorption experiment has been applied to study the reaction of the Cl-2 radical anion with dissolved sulfur(IV). For the reactions Cl-2+HSO-32Cl-+H++SO-3 (R-8) and Cl-2+SO2-32Cl-+SO-3 (R-9) rate coefficients of k8=(1.7±0.2)108 lmol-1s-1 (T=298 K, I0) and of k9=(6.2±0.3)107 lmol-1s-1 (T=279 K, I0) were obtained. 相似文献
106.
A new scheme, the lattice-sum-emulated reaction-field (LSERF) method, is presented that combines the lattice-sum (LS) and reaction-field (RF) approaches for evaluating electrostatic interactions in molecular simulations. More precisely, the LSERF scheme emulates a RF calculation (based on an atomic cutoff) via the LS machinery. This is achieved by changing the form of the electrostatic interactions in a standard LS calculation (Coulombic) to the form corresponding to RF electrostatics (Coulombic plus quadratic reaction-field correction term, truncated at the cutoff distance). It is shown (both analytically and numerically) that in the limit of infinite reciprocal-space accuracy, (i) the LSERF scheme with a finite reaction-field cutoff and a given reaction-field permittivity is identical to the RF scheme with the same parameters (and an atomic cutoff), and (ii) the LSERF scheme is identical to the LS scheme in the limit of an infinite reaction-field cutoff, irrespective of the reaction-field permittivity. This new scheme offers two key advantages: (i) from a conceptual point of view, it shows that there is a continuity between the RF and LS schemes and unifies them into a common framework; (ii) from a practical point of view, it allows us to perform RF calculations with arbitrarily large reaction-field cutoff distances for the same computational costs as a corresponding LS calculation. The optimal choice for the cutoff will be the one that achieves the best compromise between artifacts arising from the dielectric heterogeneity of the system (short cutoff) and its artificial periodicity (long cutoff). The implementation of the LSERF method is extremely easy, requiring only very limited modifications of any standard LS code. For practical applications to biomolecular systems, the use of the LSERF scheme with large reaction-field cutoff distances is expected to represent a significant improvement over the current RF simulations involving comparatively much shorter cutoffs. 相似文献
107.
The intensity of coherent anti-Stokes resonance Raman scattering (CARRS) is calculated taking into account the resonant absorption of laser and anti-Stokes waves and changes in the molecule population. The resonant absorption causes an alteration of the phase of the laser wave leading to a decrease and periodic behaviour of the anti-Stokes intensity. This phase change can be compensated by the choice of a definite wave vector mismatchK, which determines the optimum condition for the CARRS. The optimum angle between the Stokes and the laser propagation direction and the optimum cell length are calculated. The line shape of the CARRS is discussed and used for the explanation of the observed dependence of the CARRS spectra on the laser intensity and the frequency and on the molecule number density. In the case of a O-O excitation the vibrational frequencies of the ground and the excited level are generated simultaneously in the CARRS spectra. 相似文献
108.
109.
110.