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91.
Len Sherman 《电子产品世界》2004,(9):59-61
USB标准其中一个特性是从主机为插入的USB外设供电.从过去的串行和并行端口变化到USB,这种进步可使连接到PC的各种器件数大大增加. 相似文献
92.
John Sherman 《Alternatives to the High Cost of Litigation》2008,26(3):59-61
Two CPR Fall 2007 Meeting panelists re‐team to expand their focus on corporate social responsibility and its relationship to conflict resolution. First, John Sherman, of Westborough, Mass., describes why his employer, energy provider National Grid, focuses substantial business efforts on giving communities a voice in its efforts. Caroline Rees, of Cambridge, Mass., examines the need for grievance mechanisms to address inevitable local conflicts. Both authors provide practical advice based on adaptable existing models. 相似文献
93.
94.
Aika Kai Hikaru Kato David H. Sherman Robert M. Williams Sachiko Tsukamoto 《Tetrahedron letters》2018,59(48):4236-4240
A new prenylated indoxyl alkaloid, Amoenamide B (1), was isolated from Aspergillus amoenus NRRL 35600 along with Asperochramide A (2). Although many prenylated oxindole alkaloids, containing bicyclo[2.2.2]diazaoctane cores, have been isolated from the fungus of the genera Aspergillus and Penicillium to date, 1 is the fourth compound with the indoxyl unit containing the cores. During the structure elucidation of 1, we found that the planar structure matched to that of Speramide A (3), isolated from A. ochraceus KM007, but the reported structure of 3 was incorrect and turned out to be that of Taichunamide H (4), recently isolated from A. versicolor HDN11-84. 相似文献
95.
96.
Miller KA Welch TR Greshock TJ Ding Y Sherman DH Williams RM 《The Journal of organic chemistry》2008,73(8):3116-3119
The biomimetic total syntheses of both malbrancheamide and malbrancheamide B are reported. The synthesis of the two monochloro species enabled the structure of malbrancheamide B to be unambiguously assigned. The syntheses each feature an intramolecular Diels-Alder reaction of a 5-hydroxypyrazin-2(1H)-one to construct the bicyclo[2.2.2]diazaoctane core, which has also been proposed as the biosynthetic route to these compounds. 相似文献
97.
Scarpellini M Gätjens J Martin OJ Kampf JW Sherman SE Pecoraro VL 《Inorganic chemistry》2008,47(9):3584-3593
In view of the biological and commercial interest in models for Oxalate Decarboxylases (OxDC) and Oxalate Oxidases (OxOx), we have synthesized and characterized three new Mn (II) complexes ( 1- 3) employing N3O-donor amino-carboxylate ligands (TCMA, 1,4,7-triazacyclononane- N-acetic acid; K (i) Pr 2TCMA, potassium 1,4-diisopropyl-1,4,7-triazacyclononane- N-acetate; and KBPZG, potassium N,N-bis(3,5-dimethylpyrazolyl methyl)glycinate). These complexes were characterized by several techniques including X-ray crystallographic analysis, X-band electron paramagnetic resonance (EPR), electrospray ionization mass spectrometry (ESI-MS), and cyclic voltammetry. The crystal structures of 1 and 3 revealed that both form infinite polymeric chains of Mn (II) complexes linked by the pendant carboxylate arms of the TCMA (-) and the BPZG (-) ligands in a syn-antipattern. Complex 2 crystallizes as a mononuclear Mn (II) cation, six-coordinate in a distorted octahedral geometry. Although complexes 1 and 3 crystallize as polymeric chains, all compounds present the same N3O-donor set atoms around the metal center as observed in the crystallographically characterized OxDC and OxOx. Moreover, complex 2 also contains two water molecules coordinated to the Mn center as observed in the active site of OxDC and OxOx. ESI-MS spectrometry, combined with EPR, were useful techniques to establish that complexes 1- 3 are present as mononuclear Mn (II) species in solution. Finally, complexes 1- 3 are able to model the resting state active sites, with special attention focused on complex 2 which provides the first exact first coordination sphere ligand structural model for the resting states of both OxDC and OxOx. 相似文献
98.
Disinfection and Mechanistic Insights of Escherichia coli in Water by Bismuth Oxyhalide Photocatalysis
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Ilana Sherman Yoram Gerchman Yoel Sasson Hani Gnayem Hadas Mamane 《Photochemistry and photobiology》2016,92(6):826-834
This study demonstrates the potential of a new BiOCl0.875Br0.125 photocatalyst to disinfect Escherichia coli in water under simulated solar irradiation. Photocatalytic efficiency was examined for different photocatalyst loadings, solar wavelengths, exposure times, photocatalyst concentration × contact time (Ct) concept and with the use of scavengers. To elucidate the inactivation mechanism, we examined DNA damage, membrane damage, lipid peroxidation and protein release. Both photolysis and photocatalysis were negligible under visible irradiation, but enhanced photocatalytic activity was observed under solar UVA (λ > 320 nm) and UVB (λ > 280 nm), with 1.5 and 3.6 log inactivation, respectively, after 40 min of irradiation. The log inactivation vs Ct curve for E. coli by UVA/BiOCl0.875Br0.125 was fairly linear, with Ct = 10 g L?1 × min, resulting in 2 log inactivation. Photocatalytic treatment led to membrane damage, but without lipid peroxidation. Accordingly, protein was released from the cells after UVA or UVA/BiOCl0.875Br0.125 treatment. Photocatalysis also increased endonuclease‐sensitive sites vs photolysis alone, by an unknown mechanism. Finally, E. coli inactivation was not influenced by the addition of tert‐butanol or l ‐histidine, implying that neither hydroxyl radicals nor singlet oxygen reactive species are involved in the inactivation process. 相似文献
99.
100.
An approach to the assessment of the limit of detection and the limit of quantitation using uncertainty calculation is discussed.
The approach is based on the known evaluation of the limits of detection and quantitation as concentrations of the analyte
equal to three and ten standard deviations of the blank response, respectively. It is shown that these values can be calculated
as the analyte concentrations, for which relative expanded uncertainty achieves 66% and 20% of possible results of the analyte
determination, correspondingly. For example, the calculation is performed for the validation of a new method for water determination
in the presence of ene-diols or thiols, developed for analysis of chemical products, drugs or other materials which are unsuitable
for direct Karl Fischer titration. A good conformity between calculated values and experimental validation data is observed.
Received: 27 July 1998 · Accepted: 29 November 1998 相似文献