全文获取类型
收费全文 | 145篇 |
免费 | 9篇 |
国内免费 | 2篇 |
专业分类
化学 | 112篇 |
力学 | 2篇 |
数学 | 21篇 |
物理学 | 21篇 |
出版年
2024年 | 1篇 |
2023年 | 4篇 |
2022年 | 2篇 |
2021年 | 4篇 |
2020年 | 9篇 |
2019年 | 6篇 |
2018年 | 7篇 |
2017年 | 2篇 |
2016年 | 3篇 |
2015年 | 5篇 |
2014年 | 6篇 |
2013年 | 7篇 |
2012年 | 11篇 |
2011年 | 16篇 |
2010年 | 6篇 |
2009年 | 4篇 |
2008年 | 10篇 |
2007年 | 10篇 |
2006年 | 11篇 |
2005年 | 7篇 |
2004年 | 6篇 |
2003年 | 3篇 |
2002年 | 6篇 |
2001年 | 1篇 |
2000年 | 3篇 |
1999年 | 1篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1989年 | 1篇 |
1978年 | 1篇 |
排序方式: 共有156条查询结果,搜索用时 375 毫秒
21.
Applied Biochemistry and Biotechnology - Two alternative enzymatic routes to continuous biological acetaldehyde production from ethanol by immobilized yeast were compared: ADH ofCandida utilis and... 相似文献
22.
Xu M Elmatad YS Sebastianelli F Moskowitz JW Bacić Z 《The journal of physical chemistry. B》2006,110(49):24806-24811
We report quantum five-dimensional (5D) calculations of the energy levels and wave functions of the hydrogen molecule, para-H2 and ortho-H2, confined inside the small dodecahedral (H2O)20 cage of the sII clathrate hydrate. All three translational and the two rotational degrees of freedom of H2 are included explicitly, as fully coupled, while the cage is treated as rigid. The 5D potential energy surface (PES) of the H2-cage system is pairwise additive, based on the high-quality ab initio 5D (rigid monomer) PES for the H2-H2O complex. The bound state calculations involve no dynamical approximations and provide an accurate picture of the quantum 5D translation-rotation dynamics of H2 inside the cage. The energy levels are assigned with translational (Cartesian) and rotational quantum numbers, based on calculated root-mean-square displacements and probability density plots. The translational modes exhibit negative anharmonicity. It is found that j is a good rotational quantum number, while the threefold degeneracy of the j = 1 level is lifted completely. There is considerable translation-rotation coupling, particularly for excited translational states. 相似文献
23.
Amit Kumar Trevor Janes Subrata Chakraborty Prosenjit Daw Niklas vonWolff Raanan Carmieli Yael Diskin‐Posner David Milstein 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(11):3411-3415
We report a C?C bond‐forming reaction between benzyl alcohols and alkynes in the presence of a catalytic amount of KOtBu to form α‐alkylated ketones in which the C=O group is located on the side derived from the alcohol. The reaction proceeds under thermal conditions (125 °C) and produces no waste, making the reaction highly atom efficient, environmentally benign, and sustainable. Based on our mechanistic investigations, we propose that the reaction proceeds through radical pathways. 相似文献
24.
Shiran Aharon Dr. Shanti Gopal Patra Prof. Dr. Dan Meyerstein Dr. Eyal Tzur Dr. Dror Shamir Dr. Yael Albo Prof. Dr. Ariela Burg 《Chemphyschem》2023,24(22):e202300517
The Na3[Ru2(μ-CO3)4] complex is acting as a water oxidation catalyst in a homogeneous system. Due to the significance of heterogeneous systems and the effect of bicarbonate on the kinetic, we studied the bicarbonate effect on the heterogeneous electrocatalyst by entrapping the Na3[Ru2(μ-CO3)4] complex in a sol-gel matrix. We have developed two types of sol-gel electrodes, which differ by the precursor, and are demonstrating their stability over a minimum of 200 electrochemical cycles. The pH increases affected the currents and kcat for both types of electrodes, and their hydrophobicity, which was obtained from the precursor type, influenced the electrocatalytic process rate. The results indicate that NaHCO3 has an important role in the catalytic activity of the presented heterogeneous systems; without NaHCO3, the diffusing species is probably OH−, which undergoes diffusion via the Grotthuss mechanism. To the best of our knowledge, this is the first study to present a simple and fast one-step entrapment process for the Na3[Ru2(μ-CO3)4] complex by the sol-gel method under standard laboratory conditions. The results contribute to optimizing the WSP, ultimately helping expand the usage of hydrogen as a green and more readily available energy source. 相似文献
25.
Dr. Yaoyu Liang Dr. Irena Efremenko Dr. Yael Diskin-Posner Dr. Liat Avram Prof. Dr. David Milstein 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2024,136(21):e202401702
Bond activation and catalysis using s-block metals are of great significance. Herein, a series of calcium pincer complexes with deprotonated side arms have been prepared using pyridine-based PNP and PNN ligands. The complexes were characterized by NMR and X-ray crystal diffraction. Utilizing the obtained calcium complexes, unprecedented N2O activation by metal-ligand cooperation (MLC) involving dearomatization-aromatization of the pyridine ligand was achieved, generating aromatized calcium diazotate complexes as products. Additionally, the dearomatized calcium complexes were able to activate the N−H bond as well as reversibly activate H2, offering an opportunity for the catalytic hydrogenation of various unsaturated molecules. DFT calculations were applied to analyze the electronic structures of the synthesized complexes and explore possible reaction mechanisms. This study is an important complement to the area of MLC and main-group metal chemistry. 相似文献
26.
27.
Immunosensors are powerful analytical tools in clinical and veterinary diagnostics. This has led us to design a chemiluminescent immunosensor aimed at identifying anti-Brucella antibodies using optical fibers as the transducer. In order to develop the optimal transducer, to achieve an optimal chemical modification thereby allowing an optimal covalent binding of the protein receptor, several cleaning strategies and silane coupling agents were investigated. Brucella killed organisms were used as a model receptor for quantifying anti-Brucella IgG antibodies in a suspension compared to conventional colorimetric and chemiluminescent ELISA. A silane-benzophenone derivative was selected as the best performing silane coupling agent: the optical fiber immunosensor (OFIS) has showed the lowest limit of detection at 0.207 μg/ml, compared to 0.828 μg/ml and 0.414 μg/ml achieved by colorimetric and chemiluminescent ELISAs, respectively. These results, together with the additional advantages of rapidity, lower reagent volumes and moderate operating conditions, have set the grounds for further study in order to adapt this platform for on-site diagnostics of brucellosis disease markers. 相似文献
28.
Vogt M Gargir M Iron MA Diskin-Posner Y Ben-David Y Milstein D 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(30):9194-9197
Team work: Although CO(2) binding to metal centers usually involves π coordination to a C=O group or σ bonds to the carbon or oxygen atom of the CO(2) molecule, a new mode of metal-ligand cooperative activation of CO(2) to a ruthenium PNP pincer complex involving aromatization/dearomatization steps is presented in experimental and theoretical studies (see scheme). 相似文献
29.
Yael Pascal‐Levy Evgeny Shifman Dr. Manish Pal‐Chowdhury Eitan M. Hajaj Oleg Shtempluck Alexey Razin Valeri Kochetkov Prof. Yuval E. Yaish 《Chemphyschem》2012,13(18):4202-4206
Humidity plays an important role in molecular electronics. It facilitates charge movement on top of dielectric layers and modifies the device transfer characteristics. Using two different methods to probe temporal charge redistribution on the surface of dielectrics, we were able to extract the surface humidity for the first time. The first method is based on the relaxation time constants of the current through carbon nanotube field‐effect transistors (CNTFETs), and the second is based on electric force microscopy (EFM) measurements. Moreover, we found that applying external gate biases modifies the surface humidity. A theoretical model based on dielectrophoretic attraction between the water molecules and the substrate is introduced to explain this observation, and the results support our hypothesis. Furthermore, it is found that upon the adsorption of two to three layers of water the surface conductivity saturates. 相似文献
30.
Dr. You-Quan Zou Dr. Niklas von Wolff Dr. Michael Rauch Dr. Moran Feller Dr. Quan-Quan Zhou Dr. Aviel Anaby Dr. Yael Diskin-Posner Dr. Linda J. W. Shimon Dr. Liat Avram Yehoshoa Ben-David Prof. Dr. David Milstein 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(14):4715-4722
Glycolic acid is a useful and important α-hydroxy acid that has broad applications. Herein, the homogeneous ruthenium catalyzed reforming of aqueous ethylene glycol to generate glycolic acid as well as pure hydrogen gas, without concomitant CO2 emission, is reported. This approach provides a clean and sustainable direction to glycolic acid and hydrogen, based on inexpensive, readily available, and renewable ethylene glycol using 0.5 mol % of catalyst. In-depth mechanistic experimental and computational studies highlight key aspects of the PNNH-ligand framework involved in this transformation. 相似文献