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121.
Photodynamic efficacy of chlorin p6, a potential candidate of photodynamic therapy (PDT), has been studied at pH 5.0, 6.0 and 7.6 in aqueous and lipid environment. Increased chlorin p6 mediated photodynamic bleaching of N,N-dimethyl-4-nitrosoaniline (RNO), a measure of singlet oxygen yield, was obtained at higher pH. Rate of photodynamic bleaching of RNO was also higher at higher pH and the rate decreased with lowering in pH of irradiated solution. Photodynamic oxidation of tryptophan was also found to be higher at higher pH. Diminished oxidation of RNO was obtained with decrease in pH of irradiated solution. Both, RNO bleaching and tryptophan oxidation was significantly reduced by sodium azide, a known quencher of singlet oxygen. At lower pH, chlorin p6 mediated photodynamic malondialdehyde (MDA) and lipid hydroperoxide formation in egg lecithin liposome was higher. At higher pH chlorin p6 was found to be photodynamically more effective in aqueous environment whereas at lower pH chlorin p6 was photodynamically more effective in hydrophobic environment. 相似文献
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Tan G Ford C John VT He J McPherson GL Bose A 《Langmuir : the ACS journal of surfaces and colloids》2008,24(3):1031-1036
The solubilization of phenols in micelles of cetyltrimethyl ammonium bromide leads to microstructural changes from spherical micelles to wormlike micelles and then to vesicles. These microstructures are then used to template silicas. There is a transition from highly ordered hexagonal mesoporous silicas of the M41S family to lamellar structures, as the phenolic dopant concentration is increased. The results have implication to the removal of phenols from aqueous waste streams through the micellar enhanced ultrafiltration process. The entrapment of phenols in mesoporous silicas provides a way to sequester such contaminants in concentrated form. 相似文献
123.
Summary: Degradation of a polymer in a reactor by the degrading agent(s) follows a distinct pattern, primarily influenced by structural integrity and reactor environment. This distinct pattern is recorded in the changes in the evolved molecular weight distribution (MWD) or polymer chain length distribution (PCLD) curve characteristics from the initial intact state. Modern size exclusion chromatography (SEC) is the best laboratory‐based method that can clearly provide these plots in the form of chromatogram; however, detailed molecular information is not available. The nature of molecular destruction can be well‐characterised if the distinct MWD shift patterns can be simulated to fingerprint the different chain scission dynamics. This is investigated by our current research using the power of computer simulation techniques to gain insight into the polymer ageing processes. One such technique for studying simple decay processes is presented here, and the results are compared with experimental findings. The concept of a binary tree scission model is introduced to show chain rupture as a sequence of probabilistic events and as a non‐linear function of time. Two new mathematical algorithms, an iterative Monte Carlo structured probability scheme and a semi‐iterative algebraic exact statistical formulation method, are investigated to implement this model and simulate the evolution of resultant temporal MW distribution. The latter, an innovative approach to mathematical modelling, has the potential to generate a statistically perfect instant MWD decay curve. A statistical comparison of the product yield is presented from the data obtained using a wide variety of simulated scission regimes to determine the sources of variability.
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S. P. Mushran A. K. Bose J. N. Tiwari 《Monatshefte für Chemie / Chemical Monthly》1976,107(4):1021-1027
N-bromosuccinimide oxidation of cyclopentanone in acidic media in presence of mercuric acetate has been made. A zero order dependance to N-bromosuccinimide and a first order dependence to cyclopentanone and hydrogen ion concentration has been observed. Ionic strength, mercuric acetate and succinimide has negligible effect while methanol addition has a positive effect. Various rate parameters have been computed and 1,2-cyclopentanedione identified as the end product. A suitable mechanism in confirmity with the above observations has been proposed.With 2 Figures 相似文献
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Prosenjit Bose Vida Dujmović Ferran Hurtado Stefan Langerman Pat Morin David R. Wood 《Discrete and Computational Geometry》2009,42(4):570-585
To untangle a geometric graph means to move some of the vertices so that the resulting geometric graph has no crossings. Pach and Tardos (Discrete Comput. Geom. 28(4): 585–592, 2002) asked if every n-vertex geometric planar graph can be untangled while keeping at least n ε vertices fixed. We answer this question in the affirmative with ε=1/4. The previous best known bound was \(\Omega(\sqrt{\log n/\log\log n})\). We also consider untangling geometric trees. It is known that every n-vertex geometric tree can be untangled while keeping at least \(\Omega(\sqrt{n})\) vertices fixed, while the best upper bound was \(\mathcal{O}((n\log n)^{2/3})\). We answer a question of Spillner and Wolff (http://arxiv.org/abs/0709.0170) by closing this gap for untangling trees. In particular, we show that for infinitely many values of n, there is an n-vertex geometric tree that cannot be untangled while keeping more than \(3(\sqrt{n}-1)\) vertices fixed. 相似文献
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