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121.
122.
Jernigan FE Sieracki NA Taylor MT Jenkins AS Engel SE Rowe BW Jové FA Yap GP Papish ET Ferrence GM 《Inorganic chemistry》2007,46(2):360-362
The recently synthesized 3-tert-butyl-5-methyl-1,2,4-triazole reacted with KBH4 to give the new potassium tris(3-tert-butyl-5-methyl-1,2,4-triazolyl)borate K(Ttz(tBu,Me)) ligand. Ttz(tBu,Me) formed a four-coordinate (Ttz(tBu,Me))CoCl complex and five-coordinate (Ttz(tBu,Me))CoNO3 and (Ttz(tBu,Me))ZnOAc complexes. When these complexes were compared to their Tp(tBu,Me) analogues, it was found that Ttz(tBu,Me) resulted in negligible steric differences. K(Ttz(tBu,Me)) is more water-soluble than K(Tp(tBu,Me)), so bulky tris(triazolyl)borate ligands should lead to functional models for enzyme active sites in an aqueous environment and the creation of water-soluble analogues of Tp catalysts. 相似文献
123.
A complete reaction sequence for molecular dissociation at a surface has been characterized using density functional theory. The barriers for sequential ethane dehydrogenation on Pt{110} are found to fall into distinct energy sets: very low barriers, with values in the range of 0.29-0.42 eV, for the initial ethane dissociation to ethene and ethylidene at the surface; medium barriers, in the range of 0.72-1.10 eV, for dehydrogenation of C(2)H(4) fragments to vinylidene and ethyne; and high barriers, requiring more than 1.45 eV, for further dehydrogenation. For dissociation processes where more than one pathway has been found, the lowest energetic route links the most stable reactant adsorbed state at the surface to a product state involving the hydrocarbon moiety adsorbed in its most stable configuration at the surface. Hence there is a clear link between surface stability and kinetics for these species. 相似文献
124.
Feiler AA Stiernstedt J Theander K Jenkins P Rutland MW 《Langmuir : the ACS journal of surfaces and colloids》2007,23(2):517-522
Friction force measurements have been conducted with a colloid probe on mica and silica (both hydrophilic and hydrophobized) after long (24 h) exposure to high-humidity air. Adhesion and friction measurements have also been performed on cellulose substrates. The long exposure to high humidity led to a large hysteresis between loading and unloading in the friction measurements with separation occurring at large negative applied loads. The large hysteresis in the friction-load relationship is attributed to a contact area hysteresis of the capillary condensate which built up during loading and did not evaporate during the unloading regime. The magnitude of the friction force varied dramatically between substrates and was lowest on the mica substrate and highest on the hydrophilic silica substrate, with the hydrophobized silica and cellulose being intermediate. The adhesion due to capillary forces on cellulose was small compared to that on the other substrates, due to the greater roughness of these surfaces. 相似文献
125.
Numerical modeling via finite element analyses (FEA) and experimental measurements via moiré interferometry were applied to the investigation of abrasive waterjet (AWJ) drilling. Polycarbonate and alumina blocks with dimensions of 25.4 mm×19.5 mm×6.25 mm were subjected to concentrated static loads experimentally and numerically. The assumptions of the FEA model are verified by comparing the experimental results with the numerical solution. A closed-form solution confirmed the correlation between the two. It was concluded that the assumption of the FEA model (e.g. mesh, boundary conditions, pressure loading, etc.) represented the static conditions. This conclusion allowed the application of a hybrid numerical/experimental technique to understand the complex interaction of the target material and the AWJ slurry column during drilling. 相似文献
126.
W. Ken Busfield Ian D. Jenkins Phuc Van Le 《Journal of polymer science. Part A, Polymer chemistry》1998,36(13):2169-2176
The competitive reactions of cyanoisopropyl radicals with the mixed monomers styrene and acrylonitrile have been investigated using the nitroxide radical trapping technique. When the trap concentration is kept low, second, third, and even fourth generation (in terms of successive monomer addition) carbon radicals have been observed as trapped products. The ratio of rate constants for the addition of styrene and acrylonitrile to cyanoisopropyl radicals is 2.7 at 75°C and 5.3 at 105°C. These values are compared with the ratios for reactions of these two monomers with a number of other radicals and discussed in terms of the polarities of the radicals and monomers. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2169–2176, 1998 相似文献
127.
David J. Holt William D. Barker Paul R. Jenkins David L. Davies Shaun Garratt John Fawcett David R. Russell Subtrata Ghosh 《Angewandte Chemie (International ed. in English)》1998,37(23):3298-3300
Even eight-membered rings (such as in 2 ) can be formed by ring-closing metathesis of glucose derivatives such as 1 . Enantiomerically pure tricyclic spiro compounds can also be prepared. 相似文献
128.
129.
W. Ken Busfield Ian D. Jenkins Michael J. Monteiro 《Journal of polymer science. Part A, Polymer chemistry》1997,35(2):263-270
The radical trapping technique employing 1,1,3,3-tetramethyl-1,3-dihydro-1H-isoindol-2-yloxyl as a scavenger has been used to investigate the reaction of t-butoxyl radicals with mixtures of ethyl vinyl ether and methyl methacrylate. The range of identified products includes those from both addition and hydrogen abstraction with both monomers, head addition with ethyl vinyl ether, and some second monomer addition products. Relative rate constants have been obtained for various pairs of constituent reactions. t-Butoxyl radicals add to ethyl vinyl ether one to two times faster than to methyl methacrylate, depending on which monomer is in excess. The ratio is less than 1 in nonolefinic solvents and as high as 6 in t-butanol. This solvent effect is thought to be due to the radicals complexing to either methyl methacrylate or t-butanol (H-bonding), thereby increasing its electrophilic character. © 1997 John Wiley & Sons, Inc. 相似文献
130.
Aubrey D. Jenkins 《Journal of polymer science. Part A, Polymer chemistry》1999,37(2):113-126
50 years ago, Alfrey and Price advanced the Q‐e scheme for the interpretation of radical and monomer reactivity and the prediction of monomer reactivity ratios in radical copolymerization. Despite the early criticism of the scheme by Mayo and Walling, and its obvious fundamental shortcomings, it continues to be essentially the only such scheme in use today. However, the more soundly based Patterns of Reactivity Scheme, originally proposed in 1959, has recently been revised in such a way that it provides, in a simple way, far more accurate predictions of monomer reactivity ratios than does the Q‐e scheme. Moreover, it is equally applicable to the forecasting of chain‐transfer constants and to the understanding of the reactivity of initiator radicals. The history of investigations of radical, monomer, and transfer agent reactivity is reviewed here, including a summary of the Revised Patterns Scheme and its applications. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 113–126, 1999 相似文献