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41.
Wayne Ouellette Dr. Andrey V. Prosvirin Dr. Kelly Whitenack Kim R. Dunbar Prof. Jon Zubieta Prof. 《Angewandte Chemie (International ed. in English)》2009,48(12):2140-2143
Fixing a hole : Hydrothermal chemistry has been exploited in the preparation of a 3D framework material exhibiting 48 % accessible void volume and 1.5 % hydrogen uptake by weight at 120 kPa (see picture). The title compound also exhibits single‐chain magnetic behavior and reversible changes in magnetic properties upon solvation and desolvation.
42.
Daniel E. Lynch Ravinder Hayer Samantha Beddows Joy Howdle C. Douglas Thake 《Journal of heterocyclic chemistry》2006,43(1):191-197
Four compounds derived from 2‐aminothiazole and 2‐amino‐2‐thiazoline were prepared by coupling the respective bases with the acid chlorides of either 3‐ or 4‐(N,N‐dimethylamino)benzoic acid. Products were identified using infrared spectroscopy, 1H NMR spectroscopy and electrospray mass spectroscopy and in two cases by single‐crystal X‐ray diffraction. Of the four, N‐(thiazol‐2‐yl)‐3‐(N,N‐dimethylamino)‐benzamide (1), N‐(thiazolin‐2‐yl)‐4‐(N,N‐dimethylamino)benzamide (2), N‐(thiazolin‐2‐yl)‐3‐(N,N‐dimethylamino) benzamide (3) and N‐(thiazolin‐2‐yl)‐4‐(N,N‐dimethylamino)benzamide (4), the hydrochloride salts of compounds 3 and 4 showed anti‐inflammatory activity across a concentration range of 10?2?5 × 10?4 M while 3 (at a concentration of 10?5 M) was found to have no adverse effect on myocardial function. The X‐ray crystal structure of 2 and the 1:1 adduct structure of 3 with 3‐(N,N‐dimethylamino)benzoic acid are reported. 相似文献
43.
44.
Vysakh A. Bharathan Govind K. Raj Pattayil A. Joy Chathakudath P. Vinod 《Particle & Particle Systems Characterization》2014,31(2):236-244
Core–shell bimetallic Au@Ni nanoparticles, with gold cores and thin nickel shells with overall size less than 10 nm, are synthesized and stabilized in pure cubic (fcc) and hexagonal (hcp) phase. Due to their unique crystal, electronic, and geometric structure, they show interesting magnetic and chemical properties. The Au@Nifcc is magnetic, whereas Au@Nihcp is non‐magnetic. Both the bimetallic nanostructures are stable to surface oxidation until 150 °C and show excellent catalytic activity for p‐nitrophenol reduction reaction. 相似文献
45.
46.
Kulkarni B. Manjunatha K. Joy Muthipeedika Nibin Sajith Ayyiliath Meleveetil Prashantha C. N. Pakkath Ranjith Alshammari Mohammed B. 《Molecular diversity》2022,26(5):2893-2905
Molecular Diversity - We herein report the facile synthesis of a series of 3,5-substituted-1,2,4-oxadiazole derivatives in good to excellent yields. The anti-inflammatory potential of the newly... 相似文献
47.
Yin P Wang J Xiao Z Wu P Wei Y Liu T 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(30):9174-9178
So emulsional: Two hexavanadate-organic hybrids were synthesized and their amphiphilic properties were confirmed by forming emulsions in mixtures of water and nonpolar organic solvents, and were utilized as "emulsion catalysts" in deep desulfurization reactions (see figure). Their catalytic activities show a pH-dependent behavior, which can be explained by the size-change of emulsions and the appearance of reverse emulsions. 相似文献
48.
The palladium-catalyzed C-H fluorination of 8-methylquinoline derivatives with nucleophilic fluoride is reported. This transformation involves the use of AgF as the fluoride source in combination with a hypervalent iodine oxidant. Both the scope and mechanism of the reaction are discussed. 相似文献
49.
Debnath J Dasgupta S Pathak T 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(6):1618-1627
Ribonuclease?A (RNase A) serves as a convenient model enzyme in the identification and development of inhibitors of proteins that are members of the ribonuclease superfamily. This is principally because the biological activity of these proteins, such as angiogenin, is linked to their catalytic ribonucleolytic activity. In an attempt to inhibit the biological activity of angiogenin, which involves new blood vessel formation, we employed different dinucleosides with varied non-natural backbones. These compounds were synthesized by coupling aminonucleosides with dicarboxylic acids and amino- and carboxynucleosides with an amino acid. These molecules show competitive inhibition with inhibition constant (K(i)) values of (59±3) and (155±5) μM for RNase A. The compounds were also found to inhibit angiogenin in a competitive fashion with corresponding K(i) values in the micromolar range. The presence of an additional polar group attached to the backbone of dinucleosides was found to be responsible for the tight binding with both proteins. The specificity of different ribonucleolytic subsites were found to be altered because of the incorporation of a non-natural backbone in between the two nucleosidic moieties. In spite of the replacement of the phosphate group by non-natural linkers, these molecules were found to selectively interact with the ribonucleolytic site residues of angiogenin, whereas the cell binding site and nuclear translocation site residues remain unperturbed. Docked conformations of the synthesized compounds with RNase A and angiogenin suggest a binding preference for the thymine-adenine pair over the thymine-thymine pair. 相似文献
50.
Racowski JM Gary JB Sanford MS 《Angewandte Chemie (International ed. in English)》2012,51(14):3414-3417
Pd(IV) -fluoride complexes, some of which are remarkably insensitive to water, have been synthesized and used in the title reaction, which proceeds with high selectivity to give the product of the C(sp(3) )?F coupling (see scheme, TfO=trifluoromethanesulfonate). Preliminary mechanistic studies implicate a pathway involving dissociation of pyridine followed by direct C?F coupling at the Pd center. 相似文献