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排序方式: 共有317条查询结果,搜索用时 15 毫秒
311.
312.
K. Sreenivasulu V. Govinda P. Venkateswarlu K. Sivakumar 《Journal of Thermal Analysis and Calorimetry》2014,115(2):1805-1811
Experimental densities (ρ) and ultrasonic sound velocities (u) for the binary mixtures of toluene, o-chlorotoluene, m-chlorotoluene, and p-chlorotoluene with 1-octanol were measured over the entire composition range at T = (298.15, 303.15, and 308.15) K and at a pressure of 0.1 MPa. Excess volumes (V E), isentropic compressibilities $ (\kappa_{\text{s}} ) $ , and excess isentropic compressibilities $ (\kappa_{\text{s}}^{\text{E}} ) $ were calculated using the measured experimental densities and ultrasonic sound velocities of the pure liquids and their mixtures. The experimental data were discussed in terms of intermolecular interactions between component molecules. The measured excess properties were correlated with the Redlich–Kister polynomial equation. 相似文献
313.
Katta Venkateswarlu Gandham Satyalakshmi Kanaparthy Suneel Thummala Sreenivasulu Reddy Tuniki Venugopal Raju Biswanath Das 《Helvetica chimica acta》2008,91(11):2081-2088
Methyl 5‐formyl‐1‐benzofuran‐6‐carboxylate ( 1 ) and the two clerodane diterpenes, methyl 6‐oxocleroda‐3,13‐dien‐15,16‐olid‐18‐oate ( 2 ) and 2β‐(2‐methylbutanoyl)cleroda‐3,13‐dien‐15,16‐olid‐18‐oic acid ( 3 ), together with 15 known compounds, were isolated from the aerial parts of Pulicaria wightiana. The structures of the new compounds 1, 2 , and 3 were established by spectroscopic (mainly 1D‐ and 2D‐NMR) methods. 相似文献
314.
Vanam Shekhar Dorigondla Kumar Reddy Yenamandra Venkateswarlu 《Helvetica chimica acta》2012,95(9):1593-1599
A simple and efficient stereoselective total synthesis of (+)‐umuravumbolide ( 1b ) and (?)‐deacetylumuravumbolide ( 1a ) starting from commercially available pentanal is described. The synthesis involves Sharpless asymmetric epoxidation, Jacobsen's hydrolytic kinetic resolution (HKR), and the Yamaguchi oxirane opening as key steps (Scheme 2). 相似文献
315.
Rao RN Venkateswarlu N Khalid S Narsimha R Sridhar S 《Journal of chromatography. A》2006,1113(1-2):20-31
Three different sample preparation techniques (i) solid-phase extraction, (ii) reverse osmosis and (iii) vacuum distillation have been investigated and the recoveries were compared for determination of highly water-soluble benzene and stilbene sulfonic acids in aqueous environment by liquid chromatography with photodiode array (PDA) and electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). The recoveries were quite high using vacuum distillation (>90%) compared to solid phase extraction and reverse osmosis. The negative ion ESI mass spectra containing the peaks of quasimolecular ion [M-H]- allow the molecular mass determination of unknown compounds whereas the structures were proposed using fragments obtained from MS/MS analysis of [M-H]- ions. At lower fragmentation voltages only the quasimolecular ion [M-H]- was observed and as fragmentation voltages increased, it led to the formation of fragment ions corresponding to [M-H-SO3]-, [M-H-SO2]-, and SO3-. The detection limits were 1-28 microg/L with LC-ESI-MS. The sample collected from wastewater treatment plant was found to contain 21.1, 13.3, 12.1, 41.8 and 9.9 microg/L of cis-4,4(l)-diaminostilbene-2,2(l)-disulfonic acid (cis-DASDA), trans-4,4(l)-diaminostilbene-2,2(l)-disulfonic acid (trans-DASDA), 3-amino acetanilide-4-sulfonic acid (3-AASA), 4-chloroaniline-2-sulfonic acid (4-CASA), 2-chloroaniline-5-sulfonic acid (2-CASA), respectively. 相似文献
316.
Goh L Chen K Bhamidi V He G Kee NC Kenis PJ Zukoski CF Braatz RD 《Crystal growth & design》2010,10(6):2515-2521
The measured induction times in droplet-based microfluidic systems are stochastic and are not described by the deterministic population balances or moment equations commonly used to model the crystallization of amino acids, proteins, and active pharmaceutical ingredients. A stochastic model in the form of a Master equation is formulated for crystal nucleation in droplet-based microfluidic systems for any form of nucleation rate expression under conditions of time-varying supersaturation. An analytical solution is provided to describe the (1) time evolution of the probability of crystal nucleation, (2) the average number of crystals that will form at time t for a large number of droplets, (3) the induction time distribution, and (4) the mean, most likely, and median induction times. These expressions are used to develop methods for determining the nucleation kinetics. Nucleation kinetics are determined from induction times measured for paracetamol and lysozyme at high supersaturation in an evaporation-based high-throughput crystallization platform, which give low prediction errors when the nucleation kinetics were used to predict induction times for other experimental conditions. The proposed stochastic model is relevant to homogeneous and heterogeneous crystal nucleation in a wide range of droplet-based and microfluidic crystallization platforms. 相似文献
317.