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排序方式: 共有174条查询结果,搜索用时 718 毫秒
171.
Dr. Conor T. Kelly Sean Dunne Dr. Irina A. Kühne Dr. Andrew Barker Dr. Kane Esien Dr. Solveig Felton Dr. Helge Müller-Bunz Dr. Yannick Ortin Prof. Grace G. Morgan 《Angewandte Chemie (International ed. in English)》2023,62(18):e202217388
Reversible proton-induced spin state switching of an FeIII complex in solution is observed at room temperature. A reversible magnetic response was detected in the complex, [FeIII(sal2323)]ClO4 ( 1 ), using Evans’ method 1H NMR spectroscopy which indicated cumulative switching from low-spin to high-spin upon addition of one and two equivalents of acid. Infrared spectroscopy suggests a coordination-induced spin state switching (CISSS) effect, whereby protonation displaces the metal-phenoxo donors. The analogous complex, [FeIII(4-NEt2-sal2323)]ClO4 ( 2 ), with a diethylamino group on the ligand, was used to combine the magnetic change with a colorimetric response. Comparison of the protonation responses of 1 and 2 reveals that the magnetic switching is caused by perturbation of the immediate coordination sphere of the complex. These complexes constitute a new class of analyte sensor which operate by magneto-modulation, and in the case of 2 , also yield a colorimetric response. 相似文献
172.
Dr. Mowpriya Das Dr. Conor Hogan Robert Zielinski Milan Kubicki Dr. Maximilian Koy Canan Kosbab Simone Brozzesi Ankita Das Mike Thomas Nehring Viktoria Balfanz Juls Brühne Prof. Dr. Mario Dähne Dr. Martin Franz Prof. Dr. Norbert Esser Prof. Dr. Frank Glorius 《Angewandte Chemie (International ed. in English)》2023,62(50):e202314663
The adsorption of N-heterocyclic olefins (NHOs) on silicon is investigated in a combined scanning tunneling microscopy, X-ray photoelectron spectroscopy, and density functional theory study. We find that both of the studied NHOs bind covalently, with ylidic character, to the silicon adatoms of the substrate and exhibit good thermal stability. The adsorption geometry strongly depends on the N-substituents: for large N-substituents, an upright adsorption geometry is favored, while a flat-lying geometry is found for the NHO with smaller wingtips. These different geometries strongly influence the quality and properties of the obtained monolayers. The upright geometry leads to the formation of ordered monolayers, whereas the flat-lying NHOs yield a mostly disordered, but denser, monolayer. The obtained monolayers both show large work function reductions, as the higher density of the flat-lying monolayer is found to compensate for the smaller vertical dipole moments. Our findings offer new prospects in the design of tailor-made ligand structures in organic electronics and optoelectronics, catalysis, and material science. 相似文献
173.
Arianna O. Osgood Yunan Zheng Dr. Soumya Jyoti Singha Roy Dr. Nikolaos Biris Myer Hussain Conor Loynd Delilah Jewel Dr. James S. Italia Prof. Abhishek Chatterjee 《Angewandte Chemie (International ed. in English)》2023,62(19):e202219269
Site-specific incorporation of multiple distinct noncanonical amino acids (ncAAs) into proteins in mammalian cells is a promising technology, where each ncAA must be assigned to a different orthogonal aminoacyl-tRNA synthetase (aaRS)/tRNA pair that reads a distinct nonsense codon. Available pairs suppress TGA or TAA codons at a considerably lower efficiency than TAG, limiting the scope of this technology. Here we show that the E. coli tryptophanyl (EcTrp) pair is an excellent TGA-suppressor in mammalian cells, which can be combined with the three other established pairs to develop three new routes for dual-ncAA incorporation. Using these platforms, we site-specifically incorporated two different bioconjugation handles into an antibody with excellent efficiency, and subsequently labeled it with two distinct cytotoxic payloads. Additionally, we combined the EcTrp pair with other pairs to site-specifically incorporate three distinct ncAAs into a reporter protein in mammalian cells. 相似文献
174.
Conor L. Oates Alister S. Goodfellow Prof. Michael Bühl Prof. Matthew L. Clarke 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2023,135(3):e202212479
DFT calculations on the full catalytic cycle for manganese catalysed enantioselective hydrogenation of a selection of ketones have been carried out at the PBE0-D3PCM//RI-BP86PCM level. Mn complexes of an enantiomerically pure chiral P,N,N ligand have been found to be most reactive when adopting a facial coordination mode. The use of a new ligand with an ortho-substituted dimethylamino-pyridine motif has been calculated to completely transform the levels of enantioselectivity possible for the hydrogenation of cyclic ketones relative to the first-generation Mn catalysts. In silico evaluation of substrates has been used to identify those likely to be reduced with high enantiomer ratios (er), and others that would exhibit less selectivity; good agreements were then found in experiments. Various cyclic ketones and some acetophenone derivatives were hydrogenated with er's up to 99 : 1. 相似文献