全文获取类型
收费全文 | 229篇 |
免费 | 15篇 |
专业分类
化学 | 160篇 |
力学 | 3篇 |
数学 | 32篇 |
物理学 | 49篇 |
出版年
2023年 | 2篇 |
2022年 | 1篇 |
2021年 | 3篇 |
2020年 | 4篇 |
2019年 | 7篇 |
2018年 | 13篇 |
2017年 | 6篇 |
2016年 | 10篇 |
2015年 | 16篇 |
2014年 | 17篇 |
2013年 | 14篇 |
2012年 | 18篇 |
2011年 | 19篇 |
2010年 | 12篇 |
2009年 | 9篇 |
2008年 | 14篇 |
2007年 | 12篇 |
2006年 | 14篇 |
2005年 | 6篇 |
2004年 | 4篇 |
2003年 | 10篇 |
2002年 | 1篇 |
2001年 | 3篇 |
2000年 | 1篇 |
1999年 | 3篇 |
1998年 | 1篇 |
1997年 | 2篇 |
1996年 | 1篇 |
1995年 | 2篇 |
1994年 | 1篇 |
1993年 | 1篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1985年 | 2篇 |
1984年 | 2篇 |
1982年 | 2篇 |
1981年 | 1篇 |
1977年 | 1篇 |
1974年 | 2篇 |
1973年 | 1篇 |
1972年 | 1篇 |
1969年 | 1篇 |
1968年 | 1篇 |
排序方式: 共有244条查询结果,搜索用时 171 毫秒
1.
Square‐Planar Ruthenium(II) Complexes: Control of Spin State by Pincer Ligand Functionalization 下载免费PDF全文
Dr. Bjorn Askevold Dr. Marat M. Khusniyarov Dr. Wolfgang Kroener Dr. Klaus Gieb Prof. Paul Müller Dr. Eberhardt Herdtweck Dr. Frank W. Heinemann Dr. Martin Diefenbach Prof. Max C. Holthausen Veacheslav Vieru Prof. Liviu F. Chibotaru Prof. Sven Schneider 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(2):579-589
Functionalization of the PNP pincer ligand backbone allows for a comparison of the dialkyl amido, vinyl alkyl amido, and divinyl amido ruthenium(II) pincer complex series [RuCl{N(CH2CH2PtBu2)2}], [RuCl{N(CHCHPtBu2)(CH2CH2PtBu2)}], and [RuCl{N(CHCHPtBu2)2}], in which the ruthenium(II) ions are in the extremely rare square‐planar coordination geometry. Whereas the dialkylamido complex adopts an electronic singlet (S=0) ground state and energetically low‐lying triplet (S=1) state, the vinyl alkyl amido and the divinyl amido complexes exhibit unusual triplet (S=1) ground states as confirmed by experimental and computational examination. However, essentially non‐magnetic ground states arise for the two intermediate‐spin complexes owing to unusually large zero‐field splitting (D>+200 cm?1). The change in ground state electronic configuration is attributed to tailored pincer ligand‐to‐metal π‐donation within the PNP ligand series. 相似文献
2.
Journal of Russian Laser Research - We develop the fast nonadiabatic quantum storage of a single-photon wave packet on a three-level atom in a high-Q cavity and find optimum parameters of the... 相似文献
3.
4.
5.
Robert D. Bongard Michael Lepley Khushabu Thakur Marat R. Talipov Jaladhi Nayak Rachel A. Jones Lipinski Chris Bohl Noreena Sweeney Ramani Ramchandran Rajendra Rathore Daniel S. Sem 《BMC biochemistry》2017,18(1):10
Background
Protein tyrosine phosphatases (PTPs) like dual specificity phosphatase 5 (DUSP5) and protein tyrosine phosphatase 1B (PTP1B) are drug targets for diseases that include cancer, diabetes, and vascular disorders such as hemangiomas. The PTPs are also known to be notoriously difficult targets for designing inihibitors that become viable drug leads. Therefore, the pipeline for approved drugs in this class is minimal. Furthermore, drug screening for targets like PTPs often produce false positive and false negative results.Results
Studies presented herein provide important insights into: (a) how to detect such artifacts, (b) the importance of compound re-synthesis and verification, and (c) how in situ chemical reactivity of compounds, when diagnosed and characterized, can actually lead to serendipitous discovery of valuable new lead molecules. Initial docking of compounds from the National Cancer Institute (NCI), followed by experimental testing in enzyme inhibition assays, identified an inhibitor of DUSP5. Subsequent control experiments revealed that this compound demonstrated time-dependent inhibition, and also a time-dependent change in color of the inhibitor that correlated with potency of inhibition. In addition, the compound activity varied depending on vendor source. We hypothesized, and then confirmed by synthesis of the compound, that the actual inhibitor of DUSP5 was a dimeric form of the original inhibitor compound, formed upon exposure to light and oxygen. This compound has an IC50 of 36 μM for DUSP5, and is a competitive inhibitor. Testing against PTP1B, for selectivity, demonstrated the dimeric compound was actually a more potent inhibitor of PTP1B, with an IC50 of 2.1 μM. The compound, an azo-bridged dimer of sulfonated naphthol rings, resembles previously reported PTP inhibitors, but with 18-fold selectivity for PTP1B versus DUSP5.Conclusion
We report the identification of a potent PTP1B inhibitor that was initially identified in a screen for DUSP5, implying common mechanism of inhibitory action for these scaffolds.6.
Pavel A. Tikhonov Nataliya G. Vasilenko Marat O. Gallyamov Georgii V. Cherkaev Viktor G. Vasilev Nina V. Demchenko Mikhail I. Buzin Sergey G. Vasilev Aziz M. Muzafarov 《Molecules (Basel, Switzerland)》2021,26(11)
New multiarm stars have been synthesized based on polylithium derivatives of high-generation carbosilane dendrimers. In the synthesis of multiarm stars based on the eighth-generation dendrimer, steric hindrances were observed even during the synthesis of a polylithium initiator. Subsequently, this led to chain transfer reactions between growing arms, as well as other side effects. As a result, dense nanogel formations with a higher tendency of ordering than in classical objects of this type were isolated from the reaction mixture. The study of the rheology of multiarm stars based on sixth-generation dendrimers made it possible to determine the activation energies of viscous flow in these objects, which makes it possible to consider them as objects with a macromolecular nature and a reptation flow mechanism. 相似文献
7.
In this article, we present a Python‐based library of high quality semi‐global potential energy surfaces for 50 polyatomic molecules with up to six atoms. We anticipate that these surfaces will find widespread application in the testing of new potential energy surface construction algorithms and nuclear ro‐vibrational structure theories. To this end, we provide the ability to generate the energy derivatives required for Taylor series expansions to sixth order about any point on the potential energy surface in a range of common coordinate systems, including curvilinear internal, Cartesian, and normal mode coordinates. The PyPES package, along with FORTRAN, C, MATLAB and Mathematica wrappers, is available at http://sourceforge.net/projects/pypes-lib . © 2015 Wiley Periodicals, Inc. 相似文献
8.
Self‐Pillared,Single‐Unit‐Cell Sn‐MFI Zeolite Nanosheets and Their Use for Glucose and Lactose Isomerization 下载免费PDF全文
Dr. Limin Ren Dr. Qiang Guo Prashant Kumar Marat Orazov Dandan Xu Prof. Saeed M. Alhassan Prof. K. Andre Mkhoyan Prof. Mark E. Davis Prof. Michael Tsapatsis 《Angewandte Chemie (International ed. in English)》2015,54(37):10848-10851
Single‐unit‐cell Sn‐MFI, with the detectable Sn uniformly distributed and exclusively located at framework sites, is reported for the first time. The direct, single‐step, synthesis is based on repetitive branching caused by rotational intergrowths of single‐unit‐cell lamellae. The self‐pillared, meso‐ and microporous zeolite is an active and selective catalyst for sugar isomerization. High yields for the conversion of glucose into fructose and lactose to lactulose are demonstrated. 相似文献
9.
Arslanov R. K. Arslanov T. R. Fedorchenko I. V. Zheludkevich A. L. 《Journal of Experimental and Theoretical Physics》2020,130(1):94-100
Journal of Experimental and Theoretical Physics - The magnetic, transport, and magnetotransport properties of ferromagnetic Zn0.1Cd0.9GeAs2 + 10% MnAs and Zn0.1Cd0.9GeAs2 + 15% MnAs nanocomposites... 相似文献
10.
Shepeleva I. I. Shokurov A. V. Bogdanova L. B. Arslanov V. V. Panchenko P. A. Fedorova O. A. Selektor S. L. 《Russian Chemical Bulletin》2018,67(12):2259-2261
Russian Chemical Bulletin - It was demonstrated that, in contrast to a solution in an organic solvent, the relaxation of the excited state of a fluorophore moiety proceeds mainly radiationless upon... 相似文献