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101.
Tomasz A. Modro 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):331-336
Abstract 13C NMR shielding parameters have been determined for the N-phosphorylated aniline and O-phosphorylated phenol derivatives, Ph–Y–P(O)Z2 (Y=NH, O), and for their complexes with titanium tetrachloride. Inductive and resonance substituent constants were calculated using the dsp approach for the neutral and charged substituents. The results are compared with those for the corresponding neutral and charged acetyl derivatives. Shielding effects and substituent constants are discussed in terms of the interactions of the lone pair at Y with the aromatic ring and with the acyl center. It is concluded that no significant p π-d π back-donation from Y to the phosphorus atom operates in the systems studied. 相似文献
102.
Jozsef Béres Wesley G. Bentrude Jeno Tomasz Alan E. Sopchik 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3-4)
Abstract An investigation of the effects of changing the nature of X, nitrogen base (B), and amino substituent (R2N) on the equilibrium 1?2 was carried out. The influence of the above structural changes on the time-averaged coupling constants JAP and JBP, determined at 300 MHz, were used to follow changes in Keq. With constant R2N, small effects from variation of X and B were found. A large range in Keq arose from changes in the steric size of R2N. These results will be related to the question of the ease of chair to twist interconversion of the phosphate ring essential to the biological activities of the naturally occurring diesters, cAMP and cGMP. 相似文献
103.
Robert Łysek Ewa Woźny Marek Chmielewski 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):327-340
Chiral formates derived from propane-1,2-diol, 1,2- O -isopropylidene- f - D -xylo- and f - D -gluco-furanoses were subjected to treatment with cyclopentadienyl [tris(trimethylsilylmethyl)] titanium (IV). A mixture of the corresponding ( E )- and ( Z )- g -silylvinyl ethers were obtained with predominance of the former. It was found that in contrast to ( Z )-vinyl ethers, which give g -lactams with chlorosulfonyl isocyanate, the ( E )-vinyl ethers gave unstable cycloadducts which undergo rapid elimination reaction leading to ( E )- f , g -unsaturated amides. 相似文献
104.
Józef Drabowicz Piotr Łyżwa Jan Omelańczuk Marian Mikołajczyk 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1)
Abstract The title compound optically active t-butylphenylphosphine oxide 1 is widely used as a key substrat for the synthesis of other optically active derivatives such as α-hydroxyphosphine oxides, vinylphosphine oxides Till now, it has been obtained by a few rather laborious procedures1 相似文献
105.
Bogdan Boduszek Tomasz Olszewski Waldemar Goldeman Magdalena Konieczna 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4):787-795
The synthesis of a series of new pyridine aminomethylphosphinic acids is described. These compounds were obtained in the reaction of the corresponding pyridine aldehydes with primary amines and with ethyl phenylphosphinate, or methylphosphinate, in the presence of bromotrimethylsilane. In aqueous, strong acid solutions, pyridine aminophosphinic acids were split, forming the phenyl-, or methylphosphonic, acid and the corresponding secondary pyridyl-alkylamines. The kinetics of some observed cleavages were measured, and a mechanism of the cleavage has been proposed. 相似文献
106.
Bogumił Łaszkiewicz 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(2):421-432
The reaction mechanism of phosphorous acid and poly(vinyl alcohol) is presented. It has been found that there during this reaction mono- and diesters are formed in which most of the acid radicals are in the phosphonic form. To confirm the presence of this form in the product obtained, reactions with diethyleneamine and chloral have been carried out as characteristic tests for phosphonic groups. The occurrence of C—P bonds resistant to hydrolysis has been also found in the reaction product. 相似文献
107.
D. F. Parra P. L. Forster R. Łyszczek A. Ostasz A. B. Lugao Z. Rzączyńska 《Journal of Thermal Analysis and Calorimetry》2013,114(3):1049-1056
The aim of this study has been to gain a fundamental understanding of the mechanisms governing thermal degradation of luminescent poly(3-hydroxybutyrate) (PHB). PHB was doped with diaquatris(thenoyltrifluoroacetonate) europium(III) complex, [Eu(tta)3(H2O)2], and different luminescent systems were obtained. The thermal-stability of the luminescent films was discussed and the products of decomposition were analyzed. Thermal degradation of PHB:Eu(tta)3 x % systems (x = 0, 1, 5, 10, and 15 %) was elucidated by means of thermogravimetric analysis (TG), the thermal-stability decreases with the increase of europium complex concentration. The PHB polymer decomposed with evolution of carbon dioxide and 2-butenoic acid molecules. The TG–FTIR results, of the gaseous degradation products of PHB in nitrogen atmosphere, indicated that the polymer is stable at temperatures up to 200 °C. Polymer matrix at concentrations above 5 % decomposed with evolution of water molecules among the other gaseous products, which implied the presence of a hydrated complex in the system. The luminescent films showed more flexibility due to a loss in crystallinity, which suggested a potential usefulness in technical applications. 相似文献
108.
Monika Michel Luke Chimuka Tomasz Kowalkowski Ewa M. Cukrowska Bogusław Buszewski 《Journal of separation science》2013,36(5):986-991
An artificial neural network model of supported liquid membrane extraction process with a stagnant acceptor phase is proposed. Triazine herbicides and phenolic compounds were used as model compounds. The model is able to predict the compound extraction efficiency within the same family based on the octanol–water partition coefficient, water solubility, molecular mass and ionisation constant of the compound. The network uses the back‐propagation algorithm for evaluating the connection strengths representing the correlations between inputs (octanol–water partition coefficients logP, acid dissociation constant pKa, water solubility and molecular weight) and outputs (extraction efficiency in dihexyl ether and undecane as organic solvents). The model predicted results in good agreement with the experimental data and the average deviations for all the cases are found to be smaller than ±3%. Moreover, standard statistical methods were applied for exploration of relationships between studied parameters. 相似文献
109.
An intramolecular, organocatalyzed Michael addition has been developed to obtain biologically important 2,3‐disubstituted cis‐2,3‐dihydrobenzofurans. By using mandelic acid salts of primary aminocatalysts, derived from cinchona alkaloids, the intramolecular cyclization reaction has been developed to proceed in high yield, with moderate to good diastereoselectivity, and up to 99 % ee. Based on the absolute configuration of the formed 2,3‐disubstituted‐cis‐2,3‐dihydrobenzofurans and by considering the observed substrate scope restrictions, a mechanistic rationalization has been presented. 相似文献
110.
Pawel Mierczynski Waldemar Maniukiewicz Tomasz P. Maniecki 《Central European Journal of Chemistry》2013,11(6):912-919
The activity of monometallic Pd, Ru, Ni and Cu catalysts supported on spinel ZnAl2O4 for water gas shift reaction (WGS) was investigated. The physicochemical properties of each catalyst was studied by XRD, TPR, BET and chemisorption methods. The highest activity was obtained for Cu/ZnAl2O4 among the catalysts tested. The activation process carried out in a reducing atmosphere 5%H2-95%Ar in the case of Cu/ZnAl2O4 system lead to the catalytic activity improvement. In the case of copper catalysts, the water gas shift reaction proceeded by the redox surface mechanism between Cu0/Cu+. The PdZn alloy formation after reduction at 350°C was shown. 相似文献