全文获取类型
收费全文 | 697篇 |
免费 | 67篇 |
国内免费 | 2篇 |
专业分类
化学 | 625篇 |
力学 | 14篇 |
数学 | 59篇 |
物理学 | 68篇 |
出版年
2023年 | 13篇 |
2022年 | 14篇 |
2021年 | 29篇 |
2020年 | 34篇 |
2019年 | 17篇 |
2018年 | 9篇 |
2017年 | 10篇 |
2016年 | 56篇 |
2015年 | 30篇 |
2014年 | 38篇 |
2013年 | 28篇 |
2012年 | 53篇 |
2011年 | 74篇 |
2010年 | 21篇 |
2009年 | 12篇 |
2008年 | 51篇 |
2007年 | 44篇 |
2006年 | 43篇 |
2005年 | 28篇 |
2004年 | 33篇 |
2003年 | 18篇 |
2002年 | 24篇 |
2001年 | 7篇 |
2000年 | 3篇 |
1999年 | 3篇 |
1998年 | 2篇 |
1996年 | 5篇 |
1995年 | 8篇 |
1994年 | 3篇 |
1992年 | 3篇 |
1991年 | 2篇 |
1990年 | 2篇 |
1985年 | 5篇 |
1981年 | 2篇 |
1979年 | 2篇 |
1977年 | 3篇 |
1976年 | 3篇 |
1975年 | 2篇 |
1961年 | 1篇 |
1960年 | 1篇 |
1957年 | 3篇 |
1956年 | 3篇 |
1944年 | 2篇 |
1943年 | 1篇 |
1936年 | 1篇 |
1935年 | 1篇 |
1931年 | 1篇 |
1930年 | 1篇 |
1921年 | 1篇 |
1899年 | 2篇 |
排序方式: 共有766条查询结果,搜索用时 78 毫秒
101.
102.
103.
Romain Tessier Raj Kumar Nandi Brendan G. Dwyer Daniel Abegg Charlotte Sornay Javier Ceballos Stphane Erb Sarah Cianfrani Alain Wagner Guilhem Chaubet Alexander Adibekian Jerome Waser 《Angewandte Chemie (International ed. in English)》2020,59(27):10961-10970
Current approaches to introduce terminal alkynes for bioorthogonal reactions into biomolecules still present limitations in terms of either reactivity, selectivity, or adduct stability. We present a method for the ethynylation of cysteine residues based on the use of ethynylbenziodoxolone (EBX) reagents. The acetylene group is directly introduced onto the thiol group of cysteine and can be used for copper‐catalyzed alkyne‐azide cycloaddition (CuAAC) without further processing. Labeling proceeded with reaction rates comparable to or higher than the most often used iodoacetamide on peptides or maleimide on the antibody trastuzumab, and high cysteine selectivity was observed. The reagents were also used in living cells for cysteine proteomic profiling and displayed improved coverage of the cysteinome compared to previously reported iodoacetamide or hypervalent iodine reagents. Fine‐tuning of the EBX reagents allows optimization of their reactivity and physical properties. 相似文献
104.
Alex J. Plajer Charlotte K. Williams 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2022,134(1):e202104495
Heteroatom-containing polymers have strong potential as sustainable replacements for petrochemicals, show controllable monomer–polymer equilibria and properties spanning plastics, elastomers, fibres, resins, foams, coatings, adhesives, and self-assembled nanostructures. Their current and future applications span packaging, house-hold goods, clothing, automotive components, electronics, optical materials, sensors, and medical products. An interesting route to these polymers is the catalysed ring-opening copolymerisation (ROCOP) of heterocycles and heteroallenes. It is a living polymerization, occurs with high atom economy, and creates precise, new polymer structures inaccessible by traditional methods. In the last decade there has been a renaissance in research and increasing examples of commercial products made using ROCOP. It is better known in the production of polycarbonates and polyesters, but is also a powerful route to make N-, S-, and other heteroatom-containing polymers, including polyamides, polycarbamates, and polythioesters. This Review presents an overview of the different catalysts, monomer combinations, and polymer classes that can be accessed by heterocycle/heteroallene ROCOP. 相似文献
105.
Charlotte Menager Nathanaël Guigo Luc Vincent Nicolas Sbirrazzuoli 《Journal of polymer science. Part A, Polymer chemistry》2020,58(12):1717-1727
The curing of epoxidized linseed oil (ELO) with three different bio-based dicarboxylic acids (sebacic acid, suberic acid, and succinic acid) has been investigated. No accelerators or catalysts were used and the resulting thermosets are 100% bio-based. Structural investigations of the three crosslinked ELO resins were made using FTIR spectroscopy and TMA, that is, tensile tests, TGA, and DMA. As evidenced by FTIR measurements ELO and dicarboxylic acids reacts but no major differences can be distinguished between the dicarboxylic acids. Non-isothermal curing has been conducted by rheological and DSC measurements. Advanced isoconversional analysis applied to DSC data in association with the complex viscosity variations gives new insights into the polymerization mechanism. The length of dicarboxylic acid carbon chain modifies the reaction rate. Then, a correlation between reaction rate, activation energy, pre-exponential factors, polymerization mechanism, and change in rate-limiting step was shown. DMA and tensile tests highlight the relationship between the carbon chain length, reactivity, and thermomechanical properties. The use of succinic acid allows reaching a higher Tg and thermal stability. 相似文献
106.
Dr. Benjamin A. Chalmers Hui Xing Sevan Houston Dr. Charlotte Clark Dr. Sussan Ghassabian Dr. Andy Kuo Benjamin Cao Andrea Reitsma Cody‐Ellen P. Murray Dr. Jeanette E. Stok Dr. Glen M. Boyle Carly J. Pierce Stuart W. Littler Prof. David A. Winkler Prof. Paul V. Bernhardt Dr. Cielo Pasay Prof. James J. De Voss Prof. James McCarthy Prof. Peter G. Parsons Prof. Gimme H. Walter Prof. Maree T. Smith Prof. Helen M. Cooper Prof. Susan K. Nilsson Dr. John Tsanaktsidis Dr. G. Paul Savage Prof. Craig M. Williams 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2018,130(28):8491-8491
107.
Novofumigatonin (1), a new metabolite, has been isolated from Aspergillus novofumigatus. The structure and relative stereochemistry were determined from HR ESI MS, one- and two-dimensional NMR, and single-crystal X-ray analysis. The absolute configuration was assigned using vibrational circular dichroism in combination with density functional calculations. 相似文献
108.
Martin de Fonjaudran C Nevin A Piqué F Cather S 《Analytical and bioanalytical chemistry》2008,392(1-2):77-86
Wall paintings typically contain low concentrations of organic materials within a largely inorganic matrix and are characterised by their high porosity and long-term exposure to severe environmental conditions. The identification of organic materials within specific paint or plaster layers is challenging and the inherent characteristics of wall painting samples present further complications. Embedding materials (such as epoxy, polyester and acrylic-based resins) used to produce cross-sections often infiltrate porous and leanly bound samples, and compromise the interpretation of Fourier transform infrared attenuated total reflectance (FTIR-ATR) spectra and the qualitative identification of natural organic materials. An alternative method for the preparation of cross-sections of wall painting samples was developed using cyclododecane (C(12)H(24)) as a temporary consolidant and barrier coating to encapsulate the sample, and to provide necessary support to produce a cross-section through microtoming. Impacts of traditional and novel sample preparation techniques on the identification of organic materials with micro-FTIR-ATR were examined for both replica and real wall painting samples. 相似文献
109.
110.
Talib J Green C Davis KJ Urathamakul T Beck JL Aldrich-Wright JR Ralph SF 《Dalton transactions (Cambridge, England : 2003)》2008,(8):1018-1026
Electrospray ionisation mass spectrometry (ESI-MS) and circular dichroism (CD) spectroscopy were used to compare the binding of mononuclear nickel, ruthenium and platinum complexes to double stranded DNA (dsDNA) and quadruplex DNA (qDNA). CD studies provided evidence for the binding of intact complexes of all three metal ions to qDNA. ESI mass spectra of solutions containing platinum or ruthenium complexes and qDNA showed evidence for the formation of non-covalent complexes consisting of intact metal molecules bound to DNA. However, the corresponding spectra of solutions containing nickel complexes principally contained ions consisting of fragments of the initial nickel molecule bound to qDNA. In contrast ESI mass spectra of solutions containing nickel, ruthenium or platinum complexes and dsDNA only showed the presence of ions attributable to intact metal molecules bound to DNA. The fragmentation observed in mass spectral studies of solutions containing nickel complexes and qDNA is attributable to the lower thermodynamic stability of the former metal complexes relative to those containing platinum or ruthenium, as well as the slightly harsher instrumental conditions required to obtain spectra of qDNA. This conclusion is supported by the results of tandem mass spectral studies, which showed that ions consisting of intact nickel complexes bound to qDNA readily undergo fragmentation by loss of one of the ligands initially bound to the metal. The ESI-MS results also demonstrate that the binding affinity of each of the platinum and ruthenium complexes towards qDNA is significantly less than that towards dsDNA. 相似文献