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排序方式: 共有275条查询结果,搜索用时 62 毫秒
91.
Dr. Yuya Hu Dr. Rui Sang Dr. Robby Vroemans Guillaume Mollaert Dr. Rauf Razzaq Dr. Helfried Neumann Dr. Henrik Junge Prof. Dr. Robert Franke Dr. Ralf Jackstell Prof. Dr. Bert U. W. Maes Prof. Dr. Matthias Beller 《Angewandte Chemie (International ed. in English)》2023,62(6):e202214706
Diesters are of fundamental importance in the chemical industry and are used for many applications, e.g. as plasticizers, surfactants, emulsifiers, and lubricants. Herein, we present a straightforward and efficient method for the selective synthesis of diesters via palladium-catalyzed direct carbonylation of di- or polyols with readily available alkenes. Key-to-success is the use of a specific palladium catalyst with the “built-in-base” ligand L16 providing esterification of all alcohols and a high n/iso ratio. The synthesized diesters were evaluated as potential plasticizers in PVC films by measuring the glass transition temperature (Tg) via differential scanning calorimetry (DSC). 相似文献
92.
Miyashita K Rahman SM Seki S Obika S Imanishi T 《Chemical communications (Cambridge, England)》2007,(36):3765-3767
Oligonucleotides modified with a novel BNA analogue, 2', 4'-BNA(NC)[N-Me], were synthesized, and in comparison to 2',4'-BNA (LNA), have similarly high RNA affinity, better RNA selectivity and much higher resistance to nuclease degradation, suggesting that the novel BNA analogue may be particularly useful for antisense approaches. 相似文献
93.
S‐Doping of an Fe/N/C ORR Catalyst for Polymer Electrolyte Membrane Fuel Cells with High Power Density
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Yu‐Cheng Wang Yu‐Jiao Lai Lin Song Prof. Zhi‐You Zhou Prof. Jian‐Guo Liu Dr. Qiang Wang Dr. Xiao‐Dong Yang Chi Chen Wei Shi Yan‐Ping Zheng Muhammad Rauf Prof. Shi‐Gang Sun 《Angewandte Chemie (International ed. in English)》2015,54(34):9907-9910
Fe/N/C is a promising non‐Pt electrocatalyst for the oxygen reduction reaction (ORR), but its catalytic activity is considerably inferior to that of Pt in acidic medium, the environment of polymer electrolyte membrane fuel cells (PEMFCs). An improved Fe/N/C catalyst (denoted as Fe/N/C‐SCN) derived from Fe(SCN)3, poly‐m‐phenylenediamine, and carbon black is presented. The advantage of using Fe(SCN)3 as iron source is that the obtained catalyst has a high level of S doping and high surface area, and thus exhibits excellent ORR activity (23 A g?1 at 0.80 V) in 0.1 M H2SO4 solution. When the Fe/N/C‐SCN was applied in a PEMFC as cathode catalyst, the maximal power density could exceed 1 W cm?2. 相似文献
94.
Haroon Khan Muhammad Saeed Abdur Rauf Muhammad Atif Khan Naveed Muhammad 《Natural product research》2015,29(22):2160-2163
This study was designed to assess the susceptibility of various microorganisms and inhibition on heat-induced protein denaturation against diosgenin and santonin, isolated from Polygonatum verticillatum rhizomes. Both diosgenin and santonin showed significant zone of inhibition when studied against various Gram-positive (Bacillus subtilis, Bacillus cereus, Staphylococcus aureus and Staphylococcus epidermidis) and Gram-negative bacteria (Escherichia coli and Salmonella typhi). In antifungal assay, only santonin exhibited profound sensitivity against various fungi (Aspergillus flavus, Aspergillus niger, Trichoderma harzianum and Fusarium oxysporum) used in the test. Both diosgenin and santonin also exhibited marked attenuation on heat-induced protein denaturation in a concentration-dependent manner with EC50 values of 375 and 310 μg/mL, respectively. In conclusion, both the isolated compounds have antimicrobial potential supported by strong inhibition on protein denaturation and thus support the antimicrobial uses of plant in traditional system of treatment. 相似文献
95.
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97.
Torigoe H Rahman SM Takuma H Sato N Imanishi T Obika S Sasaki K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(9):2742-2751
Due to the instability of pyrimidine motif triplex DNA at physiological pH, triplex stabilization at physiological pH is crucial in improving its potential in various triplex-formation-based strategies in vivo, such as gene expression regulation, genomic DNA mapping, and gene-targeted mutagenesis. To this end, we investigated the thermodynamic and kinetic effects of our previously reported chemical modification, 2'-O,4'-C-aminomethylene-bridged nucleic acid (2',4'-BNA(NC)) modification of triplex-forming oligonucleotide (TFO), on triplex formation at physiological pH. The thermodynamic analyses indicated that the 2',4'-BNA(NC) modification of TFO increased the binding constant of the triplex formation at physiological pH by more than 10-fold. The number and position of the 2',4'-BNA(NC) modification in TFO did not significantly affect the magnitude of the increase in the binding constant. The consideration of the observed thermodynamic parameters suggested that the increased rigidity and the increased degree of hydration of the 2',4'-BNA(NC)-modified TFO in the free state relative to the unmodified TFO may enable the significant increase in the binding constant. Kinetic data demonstrated that the observed increase in the binding constant by the 2',4'-BNA(NC) modification resulted mainly from the considerable decrease in the dissociation rate constant. The TFO stability in human serum showed that the 2',4'-BNA(NC) modification significantly increased the nuclease resistance of TFO. Our results support the idea that the 2',4'-BNA(NC) modification of TFO could be a key chemical modification to achieve higher binding affinity and higher nuclease resistance in the triplex formation under physiological conditions, and may lead to progress in various triplex-formation-based strategies in vivo. 相似文献
98.
Muhammad Yaseen Muhammad Shakirullah Imtiaz Ahmad Ata Ur Rahman Faiz Ur Rahman Muhammad Usman Rauf Razzaq 《燃料化学学报》2012,40(6):714-720
In the current study simultaneous reactions of hydrodesulfurization(HDS) of dibenzothiophene(DBT) and reforming of methanol in a micro-autoclave reactor were studied over bi-metallic(Co-Mo/Al2O3 and Ni-Mo/Al2O3) and tri-metallic(Pd-Co-Mo/Al2O3 and Pd-Ni-Mo/Al2O3) catalyst systems which were prepared by incipient impregnation method.In situ hydrogen utilization and low Pd loadings were the major targets of this study.For comparison purpose,catalytic activity was separately determined for both the methanol reforming and HDS of DBT reactions as well.Ni based catalysts were confirmed with better activity than Co ones for both the reactions with Pd promoted ones ranking at the top i.e.Pd-Ni-Mo/Al2O3 > Ni-Mo/Al2O3 > Pd-Co-Mo/Al2O3 > Co-Mo/Al2O3 where Pd-Ni-Mo/Al2O3 showed 91% DBT conversion at 380 ℃ and 12 h reaction time.Some of the selected organic additives on catalytic activity were tested for their effect toward HDS reaction which was unique with close relation to their chemical nature.Reaction products were quantitatively and qualitatively analyzed via HPLC and GC-MS techniques respectively which helped in elucidating reaction mechanism. 相似文献
99.
Feroza Begum Yoshinori Namihira S.M. Abdur Razzak Shubi Kaijage Nguyen Hoang Hai Tatsuya Kinjo Kazuya Miyagi Nianyu Zou 《Optics & Laser Technology》2009,41(6):679-686
This paper reveals a novel dispersion compensating photonic crystal fiber (DC-PCF) for wide-band high-speed transmission systems. The finite-difference method with an anisotropic perfectly matched absorbing layers boundary condition is used to investigate the guiding properties. The designed novel DC-PCF shows that it is possible to obtain a larger negative dispersion coefficient, better dispersion slope compensation, and confinement losses less than 10?4 dB/m in the entire S+C+L telecommunication band by using a modest number of design parameters. The proposed module can be used in 40 Gb/s dense wavelength division multiplexing (DWDM) systems in optical fiber communication networks. 相似文献
100.
Shah Md. Abdur Rauf Mohamed Ismael Kamlesh Kumar Sahu Ai Suzuki Riadh Sahnoun Michihisa Koyama Hideyuki Tsuboi Nozomu Hatakeyama Akira Endou Hiromitsu Takaba Carlos A. Del Carpio Momoji Kubo Akira Miyamoto 《Chemical Papers》2009,63(6):654-661
Tumor suppressor protein p53 becomes inactive due to mutation on its DNA binding core domain leading to misbehavior of this protein and preventing its interaction with DNA. In the present study, changes of the protein conformation by five hot spot mutations of T-p53C were assessed preventing the mutants wild-type (WT) behavior. While studies of this nature were undertaken both experimentally and theoretically, the focus is fundamentally on the effects of the mutation on the dynamics of the protein. Hence, the basic concept underlying this study is the change in flexibility or rigidity of the protein. It was found that stable variant T-p53C (PDB-ID: 1uol) that is structurally and functionally very close to wild-type p53 is the most rigid structure and each single carcinogenic mutation on it makes the structure more flexible. We hypothesize that these changes of the molecule’s flexibility disrupt the network of hydrogen bonds associated with the interaction of WT not only at interaction but in the internal structures of the mutants as well, which prevents them from interacting in the WT fashion loosing the anti-cancer properties of WT. 相似文献