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排序方式: 共有188条查询结果,搜索用时 328 毫秒
21.
Reverdito Ana María García Mariano Hernán Salerno Alejandra Locani Oscar Alberto Perillo Isabel Amalia 《平面色谱法杂志一现代薄层色谱法》2007,20(3):227-230
JPC – Journal of Planar Chromatography – Modern TLC - When the components of a reaction mixture cannot be quantified by UV-visible spectrophotometry, because the λmax values of... 相似文献
22.
A Highly Effective Ruthenium System for the Catalyzed Dehydrogenative Cyclization of Amine–Boranes to Cyclic Boranes under Mild Conditions
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Dr. Christopher J. Wallis Dr. Gilles Alcaraz Dr. Alban S. Petit Dr. Amalia I. Poblador‐Bahamonde Dr. Eric Clot Dr. Christian Bijani Dr. Laure Vendier Dr. Sylviane Sabo‐Etienne 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(37):13080-13090
We recently disclosed a new ruthenium‐catalyzed dehydrogenative cyclization process (CDC) of diamine–monoboranes leading to cyclic diaminoboranes. In the present study, the CDC reaction has been successfully extended to a larger number of diamine–monoboranes ( 4 – 7 ) and to one amine–borane alcohol precursor ( 8 ). The corresponding NB(H)N‐ and NB(H)O‐containing cyclic diaminoboranes ( 12 – 15 ) and oxazaborolidine ( 16 ) were obtained in good to high yields. Multiple substitution patterns on the starting amine–borane substrates were evaluated and the reaction was also performed with chiral substrates. Efforts have been spent to understand the mechanism of the ruthenium CDC process. In addition to a computational approach, a strategy enabling the kinetic discrimination on successive events of the catalytic process leading to the formation of the NB(H)N linkage was performed on the six‐carbon chain diamine–monoborane 21 and completed with a 15N NMR study. The long‐life bis‐σ‐borane ruthenium intermediate 23 possessing a reactive NHMe ending was characterized in situ and proved to catalyze the dehydrogenative cyclization of 1 , ascertaining that bis σ‐borane ruthenium complexes are key intermediates in the CDC process. 相似文献
23.
de Regil-Hernández R Martínez-Lagos F Rodríguez-Bayón A Sinisterra JV 《Chemical & pharmaceutical bulletin》2011,59(9):1089-1093
Different green synthesis of alkyl esters of acyclovir (acyclovir prodrugs) is described. Hexanoic, decanoic, dodecanoic and tetradecanoic acyclovir esters were synthesized reacting acyclovir and the respective acid anhydride in dimethyl sulfoxide (DMSO), in solvents from renewable sources and without solvent (T=30 °C). Yields in prodrugs after 10 min of reaction were >95% using DMSO as solvent. The purification methodology was very simple, shorter and greener than previously described. The biosolvent, N,N-dimethylamide of decanoic acid, let us to obtain >95% yield at 24 h. This oily biosolvent is not dermotoxic and the reaction crude can directly be used in topic formulations. Syntheses without solvent proceeded successfully for acyclovir esters. Indeed, dodecanoate and tetradecanoate yielding >98% conversion of reactants in 30 min. In spite of requiring mild temperature (65 °C), substrate molar ratios were lowered to 1 : 1, thus conducing to a more efficient use of raw materials. The synthetic procedures were scaled up to a 300 g batch (yield 98-99% isolated ester). These esters can be used as acyclovir prodrugs in topic formulations. The esters release from an oil/water micro-emulsion and a hydrogel formulation were tested with good results. 相似文献
24.
Bernabé L. Rivas Julio Sánchez S. Amalia Pooley Luis Basaez Eduardo Pereira Christophe Bucher Guy Royal Eric Saint Aman Jean-Claude Moutet 《Macromolecular Symposia》2010,296(1):416-428
Arsenic species can be removed from aqueous solutions using the liquid-phase polymer-based retention, LPR, technique. The LPR technique removes ionic species by functional groups of water-soluble polyelectrolytes (WSP) and then using a ultrafiltration membrane that does not let them pass through the membrane, thus separating them from the solution. The ability of WSP with groups (R)4N+X− to remove arsenate ions using LPR was studied. The interaction and arsenate anion retention capacity depended on: pH, the quaternary ammonium group's counter ion, and the ratio polymer: As(V), using different concentrations of As(V). Water-soluble polychelates were also used for one-step retention of As(III) in solution. The complex of poly(acrylic acid)-Sn, 10 and 20 wt-% of metal gave a high retention of As(III) species at pH 8, although the molar ratio polychelate: As(III) was 400:1. The enrichment method was used to determine the maximum retention capacity (C) for arsenate anions in aqueous solutions at pH 8. In similar conditions, the values of C were 142 mg g−1 for P(ClAETA) and 75 mg g−1 for P(SAETA). The combined treatment of arsenic aqueous solutions by electrocatalytic oxidation (EO) to convert the species of As(III) to As(V) with the LPR technique quantitatively removed arsenic. 相似文献
25.
26.
Utamima Amalia Reiners Torsten Ansaripoor Amir H. 《Annals of Operations Research》2022,316(2):955-977
Annals of Operations Research - In recent years, operations research in agriculture has improved the harvested yield, reduced the cost and time required for field operations, and maintained... 相似文献
27.
We report the evaluation of the topography of an object with projected fringes generated with a lateral cyclic shear interferometer (CSI) and we then compare the topography recovery obtained with the proposed method with the one obtained from a coordinate measuring machine (CMM). We also study how the fringes visibility along the z axis affects the retrieval. Finally, we discuss the advantages and drawbacks of this profilometry system. 相似文献
28.
Prof. Chien-Wei Chu Amalia Rizki Fauziah Prof. Li-Hsien Yeh 《Angewandte Chemie (International ed. in English)》2023,62(26):e202303582
The design of ion-selective membranes is the key towards efficient reverse electrodialysis-based osmotic power conversion. The tradeoff between ion selectivity (output voltage) and ion permeability (output current) in existing porous membranes, however, limits the upgradation of power generation efficiency for practical applications. Thus, we provide the simple guidelines based on fundamentals of ion transport in nanofluidics for promoting osmotic power conversion. In addition, we discuss strategies for optimizing membrane performance through analysis of various material parameters in membrane design, such as pore size, surface charge, pore density, membrane thickness, ion pathway, pore order, and ionic diode effect. Lastly, a perspective on the future directions of membrane design to further maximize the efficiency of osmotic power conversion is outlined. 相似文献
29.
The redox reaction Br− + BrO3− has been studied in aqueous zwitterionic micellar solutions of N‐tetradecyl‐N, N‐dimethyl‐3‐ammonio‐1‐propanesulfonate, SB3‐14, and N‐hexadecyl‐N,N‐dimethyl‐3‐ammonio‐1‐propanesulfonate, SB3‐16. A simple expression for the observed rate constant, kobs, based on the pseudophase model, could explain the influences of changes in the surfactant concentration on kobs. The kinetic effect of added NaClO4 on the reaction rate in SB3‐14 micellar solutions has also been studied. They were rationalized by considering the binding of the perchlorate anions to the sulfobetaine micelles and their competition with the reactive bromide ions for the micellar surface. © 2000 John Wiley & Sons, Inc. Int J Chem Kinet 32: 388–394, 2000 相似文献
30.