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91.
Silanylidene and Germanylidene Anions: Valence‐Isoelectronic Species to the Well‐Studied Phosphinidene 下载免费PDF全文
Dr. Mujahuddin M. Siddiqui Dr. Soumen Sinhababu Sayan Dutta Dr. Subrata Kundu Paul Niklas Ruth Annika Münch Dr. Regine Herbst‐Irmer Prof. Dietmar Stalke Dr. Debasis Koley Prof. Herbert W. Roesky 《Angewandte Chemie (International ed. in English)》2018,57(36):11776-11780
The reduction of TipMCl3 (Tip=2,4,6‐triisopropylphenyl) (M=Si, Ge) with KC8 in the presence of cyclic alkyl(amino) carbene (cAAC) afforded the acyclic silanylidene and germanylidene anions in the form of potassium salt [K(cAAC)MTip]2 (M=Si ( 1 ); Ge ( 2 )). The silanylidene and germanylidene anions are valence‐isoelectronic to the well‐studied phosphinidene and are a new class of acyclic anions of Group 14. Compounds 1 and 2 were isolated and well characterized by NMR and single‐crystal X‐ray structure analysis. Furthermore, the structure and bonding of compounds 1 and 2 was investigated by computational methods. 相似文献
92.
Apostolico L Braunschweig H Crawford AG Herbst T Rais D 《Chemical communications (Cambridge, England)》2008,(4):497-498
The first catalytic application of the Group VI metal borylene complexes [(CO)(5)M[double bond]BN(SiMe(3))(2)] involves the demercuration reaction of bis(alkynyl)mercurials, [Hg(C[triple bond]CR)(2)], with formation of a series of buta-1,3-diynes. 相似文献
93.
We give a constructive proof for the existence of a Bloch basis of rank \({N}\) which is both smooth (real analytic) and periodic with respect to its \({d}\)-dimensional quasi-momenta, when \({1\leq d\leq 2}\) and \({N\geq 1}\). The constructed Bloch basis is conjugation symmetric when the underlying projection has this symmetry, hence the corresponding exponentially localized composite Wannier functions are real. In the second part of the paper, we show that by adding a weak, globally bounded but not necessarily constant magnetic field, the existence of a localized basis is preserved. 相似文献
94.
95.
Alejandro Madrid Ana Lizeth Morales Valentina Saffirio Mauricio A. Cuellar Enrique Werner Bastin Said Patricio Godoy Nelson Caro Mirna Melo Ivn Montenegro 《Molecules (Basel, Switzerland)》2021,26(21)
In this study, the essential oil (EO) from Laurelia sempervirens was analyzed by GC/MS and safrole (1) was identified as the major metabolite 1, was subjected to direct reactions on the oxygenated groups in the aromatic ring and in the side chain, and eight compounds (4 to 12) were obtained by the process. EO and compounds 4–12 were subjected to biological assays on 24 strains of the genus Saprolegnia, specifically of the species 12 S. parasitica and 12 S. australis. EO showed a significant effect against Saprolegnia strains. Compound 6 presents the highest activity against two resistant strains, with minimum inhibitory concentration (MIC) and minimum oomyceticidal concentration (MOC) values of 25 to 100 and 75 to 125 µg/mL, respectively. The results show that compound 6 exhibited superior activities compared to the commercial controls bronopol and azoxystrobin used to combat these pathogens. 相似文献
96.
97.
98.
Jhon F. Perez Elizabeth Florez Cacier Z. Hadad Patricio Fuentealba Albeiro Restrepo 《ChemInform》2008,39(39):no-no
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option. 相似文献
99.
Extraction of molybdenum and technetium with diamides of dipicolinic acid from nitric acid solutions
J. L. Lapka A. Paulenova M. Yu. Alyapyshev V. A. Babain R. S. Herbst J. D. Law 《Journal of Radioanalytical and Nuclear Chemistry》2009,280(2):307-313
The concentration of molybdenum(VI) in dissolved spent nuclear fuel is comparable with the concentrations of Tc, and the minor
actinides (Np, Am). Therefore it is of great interest to understand its behavior under conditions imposed by separation processes.
The simultaneous extraction ability of ortho, meta, and para isomers of N,N′-diethyl-N,N′-ditolyl-dipicolinamide (EtTDPA) for molybdenum and technetium were investigated in a large range of nitric and hydrochloric
acid conditions. Molybdenum shows no increase in extraction at higher concentrations of nitric acid giving a solvate number
n=0 with all isomers of EtTDPA, while Mo shows great extractability from HCl. Technetium distribution ratios decrease with
increasing concentrations of nitrate showing indication of ion exchange occurring between TcO4
− and NO3
− anions. Et(m)TDPA and Et(p)TDPA show the greatest extractability, with 60% of the total technetium extracted into the organic
phase at 1M HNO3. 相似文献
100.
Holger Braunschweig Prof. Dr. Thomas Herbst Dr. Krzysztof Radacki Dr. Gernot Frenking Prof. Dr. Mehmet Ali Celik 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(44):12099-12106
We report on the hydroboration of 1‐[bis(trimethylsilyl)amino]‐2,3‐diethylborirene ( 3 ) with 9‐borabicyclo[3.3.1]nonane (9‐BBN), which led through ring‐opening to an amino(vinyl)borane. The viscous borane was subsequently converted into a crystalline borate on treatment with MeLi. Both compounds were fully characterized by multinuclear NMR spectroscopy and in case of the latter by single‐crystal X‐ray diffraction analysis. To elucidate the reaction mechanism of the unexpected boron‐carbon bond cleavage, DFT calculations of energy minima and transition states for the hydroboration were carried out. 相似文献