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81.
Waldemar Hoffmann Johanna Hofmann Kevin Pagel 《Journal of the American Society for Mass Spectrometry》2014,25(3):471-479
Recent works using ion mobility-mass spectrometry (IM-MS) have highlighted the power of this instrumental configuration to tackle one of the greatest challenges in glycomics and glycoproteomics: the existence of isobaric isomers. For a successful separation of species with identical mass but different structure via IM-MS, it is crucial to have sufficient IM resolution. In commercially available IM-MS instruments, however, this resolution is limited by the design of the instrument and usually cannot be increased at-will without extensive modifications. Here, we present a systematic approach to improve the resolving capability of IM-MS instruments using so-called energy-resolved ion mobility-mass spectrometry. The technique utilizes the fact that individual components in an isobaric mixture fragment at considerably different energies when activated in the gas phase via collision-induced dissociation (CID). As a result, certain components can be suppressed selectively at increased CID activation energy. Using a mixture of four isobaric carbohydrates, we show that each of the individual sugars can be resolved and unambiguously identified even when their drift times differ by as little as 3 %. However, the presented results also indicate that a certain difference in the gas-phase stability of the individual components is crucial for a successful separation via energy-resolved IM-MS. Figure
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Matthias Brendel Carolin Braun Dr. Frank Rominger Prof. Dr. Peter Hofmann 《Angewandte Chemie (International ed. in English)》2014,53(33):8741-8745
For a long time d10‐ML2 fragments have been known for their potential to activate unreactive bonds by oxidative addition. In the development of more active species, two approaches have proven successful: the use of strong σ‐donating ligands leading to electron‐rich metal centers and the employment of chelating ligands resulting in a bent coordination geometry. Combining these two strategies, we synthesized bis‐NHC chelate complexes of nickel(0) and platinum(0). Bis(1,5‐cyclooctadiene)nickel(0) and ‐platinum(0) react with bisimidazolium salts, deprotonated in situ at room temperature, to yield tetrahedral or trigonal‐planar bis‐NHC chelate olefin complexes. The synthesis and characterization of these complexes as well as a first example of C? C bond activation with these systems are reported. Due to the enforced cis arrangement of two NHCs, these compounds should open interesting perspectives for bond‐activation chemistry and catalysis. 相似文献
84.
Nature’s Chemical Signatures in Human Olfaction: A Foodborne Perspective for Future Biotechnology 下载免费PDF全文
Andreas Dunkel Martin Steinhaus Matthias Kotthoff Bettina Nowak Dietmar Krautwurst Peter Schieberle Thomas Hofmann 《Angewandte Chemie (International ed. in English)》2014,53(28):7124-7143
The biocatalytic production of flavor naturals that determine chemosensory percepts of foods and beverages is an ever challenging target for academic and industrial research. Advances in chemical trace analysis and post‐genomic progress at the chemistry–biology interface revealed odor qualities of nature’s chemosensory entities to be defined by odorant‐induced olfactory receptor activity patterns. Beyond traditional views, this review and meta‐analysis now shows characteristic ratios of only about 3 to 40 genuine key odorants for each food, from a group of about 230 out of circa 10 000 food volatiles. This suggests the foodborn stimulus space has co‐evolved with, and roughly match our circa 400 olfactory receptors as best natural agonists. This perspective gives insight into nature’s chemical signatures of smell, provides the chemical odor codes of more than 220 food samples, and beyond addresses industrial implications for producing recombinants that fully reconstruct the natural odor signatures for use in flavors and fragrances, fully immersive interactive virtual environments, or humanoid bioelectronic noses. 相似文献
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Uwe Schmidt Luis Werner Merle Arrowsmith Andrea Deissenberger Alexander Hermann Alexander Hofmann Stefan Ullrich James D. Mattock Alfredo Vargas Holger Braunschweig 《Angewandte Chemie (International ed. in English)》2020,59(1):325-329
The reaction of aryl‐ and amino(dihydro)boranes with dibora[2]ferrocenophane 1 leads to the formation 1,3‐trans‐dihydrotriboranes by formal hydrogenation and insertion of a borylene unit into the B=B bond. The aryltriborane derivatives undergo reversible photoisomerization to the cis‐1,2‐μ‐H‐3‐hydrotriboranes, while hydride abstraction affords cationic triboranes, which represent the first doubly base‐stabilized B3H4+ analogues. 相似文献
86.
D. Klimm P. Hofmann P. Paufler W. Reichelt U. Krbl 《Crystal Research and Technology》1991,26(5):631-637
Damping of ultrasonic waves with frequencies in the 100 kHz region was measured in the temperature region 300 … 1000 K. Two peaks could be observed (near 400 K or near 700 K, respectively). Occurrence of these peaks depends on oxygen content of the sample. The higher temperature peak is attributed to phase transition Pmmm 〈– – –〉 P 4/mmm of YBa2Cu3O7 – x. 相似文献
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Phase resolved optical emission spectroscopy of coaxial microplasma jet operated with He and Ar 总被引:1,自引:0,他引:1