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111.
The surface properties of aluminosilicates (perlites and zeolites)—potential fillers in abrasive articles—have been examined by inverse gas chromatography. The dispersive component of the surface free energy ( $ \gamma_{\text{S}}^{\text{D}} $ ) and K A and K D describing the acidity and basicity, respectively, of the fillers were used to express the surface activity of examined materials. The Flory–Huggins parameter, $ \chi_{23}^{'} , $ characterized the interactions between polymer and filler, i.e., interactions between phenolic resin and filler. Zeolites were found to be materials with an active surface layer and relatively high ability to participate in filler–resin interactions. Therefore, they might be considered as potential “replacement material” for standard fillers. The IGC-derived values mentioned above provided useful information about the behavior of fillers during the manufacture and use of abrasive articles. 相似文献
112.
Piotr Sionkowski Piotr Bedowski Natalia Kruszewska Piotr Weber Beata Marciniak Krzysztof Domino 《Entropy (Basel, Switzerland)》2022,24(6)
Albumin is one of the major components of synovial fluid. Due to its negative surface charge, it plays an essential role in many physiological processes, including the ability to form molecular complexes. In addition, glycosaminoglycans such as hyaluronic acid and chondroitin sulfate are crucial components of synovial fluid involved in the boundary lubrication regime. This study presents the influence of Na, Mg and Ca ions on human serum albumin–hyaluronan/chondroitin-6-sulfate interactions examined using molecular docking followed by molecular dynamics simulations. We analyze chosen glycosaminoglycans binding by employing a conformational entropy approach. In addition, several protein–polymer complexes have been studied to check how the binding site and presence of ions influence affinity. The presence of divalent cations contributes to the decrease of conformational entropy near carboxyl and sulfate groups. This observation can indicate the higher affinity between glycosaminoglycans and albumin. Moreover, domains IIIA and IIIB of albumin have the highest affinity as those are two domains that show a positive net charge that allows for binding with negatively charged glycosaminoglycans. Finally, in discussion, we suggest some research path to find particular features that would carry information about the dynamics of the particular type of polymers or ions. 相似文献
113.
114.
JPC – Journal of Planar Chromatography – Modern TLC - The relative lipophilicity (RM0) and specific hydrophobic surface area of eight 1,2-benzisothiazol-3(2H)-one derivatives... 相似文献
115.
Versatility and synthetic potential of 1-(trimethylsilyloxy)-1,3-butadiene, 1-(trimethylsilyloxy)penta-1,3-diene, and their methyl substituted derivatives have been demonstrated in a modular synthetic methodology of stereodefined π-conjugated unsymmetrical, symmetrical two-dimensional, and octupolar polyenal structure. 相似文献
116.
This work contains results of computer simulation researches, which define requirements for measurement conditions, which should be fulfilled so that measurement results ensure allowable errors. They define: allowable measurement errors (interferogram's scanning) and conditions, which should fulfill computer programs, so that errors introduced by mathematical operations and computer are the smallest. 相似文献
117.
Brereton Richard G. Jansen Jeroen Lopes João Marini Federico Pomerantsev Alexey Rodionova Oxana Roger Jean Michel Walczak Beata Tauler Romà 《Analytical and bioanalytical chemistry》2018,410(26):6691-6704
Analytical and Bioanalytical Chemistry - The contribution of chemometrics to important stages throughout the entire analytical process such as experimental design, sampling, and explorative data... 相似文献
118.
Wojciech Duczmal Elzbieta Śliwińska Beata Maciejewska Bogdan Marciniec Hieronim Maciejewski 《Transition Metal Chemistry》1995,20(5):435-439
Summary Trisubstituted silanes, HSiR3-n
X
n
(R = Me or Et, X = Cl, OEt, or Ph; n = 0–3) oxidatively add to the complex [RhCl(cod)(1-hexene)] (cod = cycloocta-1,5-diene) to yield [RhCl(cod)(1-hexene)(H)(SiR3)] [(1)]. Subsequent steps of hydrosilylation follow, i.e. cis-insertion of the alkene (- rearrangement) and then reductive elimination of the product, according to the general Chalk and Harrod scheme. A quantitative correlation between the second order rate constant, k
1, of the oxidative addition (followed spectrophotometrically) at 20°C in benzene solution and the structure of the trisubstituted silane represented by Stereoelectronic parameters , and E' for the SiR3-n
X
n
groups was established. The maximal hydrosilylation rate followed by g.l.c., is strongly retarded by highly electronegative substituents X on silicon and results from the elimination rate of the hydrosilylation product from (1) and the maximal concentration of (1) in solution.Dedicated to Professor K. Rühlmann on the occasion of his 65th birthday. Part XXVII in the series Catalysis of Hydrosilylation; for Part XXVI see Polish J. Appl. Chem., 38, 169 (1994). 相似文献
119.
Adam Voelkel Beata Strzemiecka 《Colloids and surfaces. A, Physicochemical and engineering aspects》2006,280(1-3):177-181
The raw material—aloxite used during the manufacturing of grinding tools was characterized by means of inverse gas chromatography (IGC). The surface properties of the different types of aloxite were determined including: (i) the specific surface area; (ii) the dispersive component of surface free energy as well as the sensitivity of this parameter on the environment humidity; and (iii) acidity and basicity of the examined surfaces. The results of our experiments proved the usefulness of IGC in the characterization of this kind of materials. 相似文献
120.
Piotr Guga Boles?aw Karwowski Damian B?aziak Magdalena Janicka Andrzej Okruszek Beata R?bowska Wojciech J. Stec 《Tetrahedron》2006,62(11):2698-2704
The SP-isomer of 5′-OH-N4-benzoyl-2′-deoxycytidine-3′-O-(2-thio-4,4-pentamethylene-1,3,2-oxathiaphospholane) undergoes DBU-promoted intramolecular cyclization providing as a sole product SP-deoxycytidine cyclic 3′,5′-O,O-phosphorothioate. Unexpectedly, the RP-counterpart yields a mixture of products consisting of RP-deoxycytidine cyclic 3′,5′-O,O-phosphorothioate and macrocyclic oligo(deoxycytidine phosphorothioate)s. The results of molecular modeling indicate that the dychotomy observed for the RP substrate may result from remarkably higher energy of the corresponding transition states, caused by the presence of bulky ‘spiro’ pentamethylene substituent at the position C4 in the oxathiaphospholane ring. 相似文献