全文获取类型
收费全文 | 24159篇 |
免费 | 1005篇 |
国内免费 | 139篇 |
专业分类
化学 | 17197篇 |
晶体学 | 198篇 |
力学 | 485篇 |
数学 | 3177篇 |
物理学 | 4246篇 |
出版年
2023年 | 175篇 |
2022年 | 152篇 |
2021年 | 306篇 |
2020年 | 485篇 |
2019年 | 468篇 |
2018年 | 315篇 |
2017年 | 271篇 |
2016年 | 729篇 |
2015年 | 618篇 |
2014年 | 745篇 |
2013年 | 1220篇 |
2012年 | 1616篇 |
2011年 | 1788篇 |
2010年 | 999篇 |
2009年 | 822篇 |
2008年 | 1434篇 |
2007年 | 1355篇 |
2006年 | 1344篇 |
2005年 | 1244篇 |
2004年 | 1092篇 |
2003年 | 823篇 |
2002年 | 682篇 |
2001年 | 257篇 |
2000年 | 231篇 |
1999年 | 200篇 |
1998年 | 209篇 |
1997年 | 288篇 |
1996年 | 299篇 |
1995年 | 265篇 |
1994年 | 292篇 |
1993年 | 285篇 |
1992年 | 248篇 |
1991年 | 180篇 |
1990年 | 211篇 |
1989年 | 179篇 |
1988年 | 188篇 |
1987年 | 171篇 |
1986年 | 159篇 |
1985年 | 271篇 |
1984年 | 257篇 |
1983年 | 177篇 |
1982年 | 197篇 |
1981年 | 183篇 |
1980年 | 181篇 |
1979年 | 163篇 |
1978年 | 194篇 |
1977年 | 180篇 |
1976年 | 136篇 |
1975年 | 132篇 |
1974年 | 157篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
1.
Maschler Tobias Strmer-Stephan Bastian Morhard Jrg Stegmaier Thomas Tilebein Meike Griepentrog Hans W. 《Annals of Operations Research》2022,314(2):577-600
Annals of Operations Research - Selecting a vegetation layer design goes along with determining its future irrigation need. Therefore, it is essential to take a design decision that is minimising... 相似文献
2.
Yersak Thomas A. Hao Fang Kang Chansoon Salvador James R. Zhang Qinglin Malabet Hernando Jesus Gonzalez Cai Mei 《Journal of Solid State Electrochemistry》2022,26(3):709-718
Journal of Solid State Electrochemistry - In this study, hot pressing was evaluated as a method of cell fabrication to increase the energy density of next-generation all-solid-state batteries with... 相似文献
3.
Javad Mashreghi Julian Ransford Thomas Ransford 《Journal of Functional Analysis》2018,274(11):3254-3262
We show that every linear functional on the Dirichlet space that is non-zero on nowhere-vanishing functions is necessarily a multiple of a point evaluation. Continuity of the functional is not assumed. As an application, we obtain a characterization of weighted composition operators on the Dirichlet space as being exactly those linear maps that send nowhere-vanishing functions to nowhere-vanishing functions.We also investigate possible extensions to weighted Dirichlet spaces with superharmonic weights. As part of our investigation, we are led to determine which of these spaces contain functions that map the unit disk onto the whole complex plane. 相似文献
4.
5.
Habarurema Gratien Gerber Thomas Mukabagorora Theonille Hosten Eric Ndayambaje Jean Bernard Betz Richard 《Transition Metal Chemistry》2020,45(1):55-63
Transition Metal Chemistry - Rhenium(I) and (VII) complexes with cyclohex-1-enylolonium cation and bridging pyridyl derivatives are reported. Additionally, the CO-bridged pyridyl and their related... 相似文献
6.
Thomas Prenveille Cyrielle Garreau Mathias Matner Dirk Dijkstra Wilhelm Oppermann Diethelm Johannsmann 《Journal of polymer science. Part A, Polymer chemistry》2019,57(5):621-629
The reactivity of urethanes based on 1,6‐hexamethylene diisocyanate (HDI) and 4,4′‐methylene diphenyl diisocyanate (MDI) was investigated at temperatures between 190 °C and 235 °C. Diurethane model compounds end‐capped with either 1‐dodecanol (D‐core‐D) or 1‐hexadecanol (H‐core‐H) were mixed and annealed at high temperature. The core was either MDI or HDI. The transurethanization reaction was followed based on the formation of the compounds (H‐core‐D). The amount of H‐core‐D and of side products, which had formed after variable annealing times, were identified with 1H NMR, FTIR, SEC, and MALDI‐TOF. Transurethanization was considerably faster for MDI‐based urethanes than for HDI‐based urethanes. Only traces of side products were formed during annealing of MDI‐based urethanes, whereas a significant amount of allophanates was formed from HDI‐based urethanes under the same conditions. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 621–629 相似文献
7.
Dr. Stefan van der Vorm Thomas Hansen Dr. Erwin R. van Rijssel Rolf Dekkers Jerre M. Madern Prof. Dr. Herman S. Overkleeft Dr. Dmitri V. Filippov Prof. Dr. Gijsbert A. van der Marel Dr. Jeroen D. C. Codée 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(29):7149-7157
The 3D shape of glycosyl oxocarbenium ions determines their stability and reactivity and the stereochemical course of SN1 reactions taking place on these reactive intermediates is dictated by the conformation of these species. The nature and configuration of functional groups on the carbohydrate ring affect the stability of glycosyl oxocarbenium ions and control the overall shape of the cations. We herein map the stereoelectronic substituent effects of the C2-azide, C2-fluoride and C4-carboxylic acid ester on the stability and reactivity of the complete suite of diastereoisomeric furanoses by using a combined computational and experimental approach. Surprisingly, all furanosyl donors studied react in a highly stereoselective manner to provide the 1,2-cis products, except for the reactions in the xylose series. The 1,2-cis selectivity for the ribo-, arabino- and lyxo-configured furanosides can be traced back to the lowest-energy 3E or E3 conformers of the intermediate oxocarbenium ions. The lack of selectivity for the xylosyl donors is related to the occurrence of oxocarbenium ions adopting other conformations. 相似文献
8.
Sarah A. Richardson Thomas M. Rawlings Joanne Muter Marc Walker Jan J. Brosens Neil R. Cameron Ahmed M. Eissa 《Macromolecular bioscience》2019,19(2)
A novel strategy for the surface functionalization of emulsion‐templated highly porous (polyHIPE) materials as well as its application to in vitro 3D cell culture is presented. A heterobifunctional linker that consists of an amine‐reactive N‐hydroxysuccinimide ester and a photoactivatable nitrophenyl azide, N‐sulfosuccinimidyl‐6‐(4′‐azido‐2′‐nitrophenylamino)hexanoate (sulfo‐SANPAH), is utilized to functionalize polyHIPE surfaces. The ability to conjugate a range of compounds (6‐aminofluorescein, heptafluorobutylamine, poly(ethylene glycol) bis‐amine, and fibronectin) to the polyHIPE surface is demonstrated using fluorescence imaging, FTIR spectroscopy, and X‐ray photoelectron spectroscopy. Compared to other existing surface functionalization methods for polyHIPE materials, this approach is facile, efficient, versatile, and benign. It can also be used to attach biomolecules to polyHIPE surfaces including cell adhesion‐promoting extracellular matrix proteins. Cell culture experiments demonstrated that the fibronectin‐conjugated polyHIPE scaffolds improve the adhesion and function of primary human endometrial stromal cells. It is believed that this approach can be employed to produce the next generation of polyHIPE scaffolds with tailored surface functionality, enhancing their application in 3D cell culture and tissue engineering whilst broadening the scope of applications to a wider range of cell types. 相似文献
9.
Maartje M. C. Bastings Thomas M. Hermans A. J. H. Spiering Erwin W. L. Kemps Lorenzo Albertazzi Eva E. Kurisinkal Patricia Y. W. Dankers 《Macromolecular bioscience》2019,19(1)
The most basic function of synthetic microenvironments for tissue engineering is to act as a physical substrate for cell attachment, migration, and proliferation, similar to the natural cell environment. Functionalization of supramolecular materials with guest compounds that display the same recognition moieties is a common strategy to introduce biofunctionality. However, besides a robust interaction with the material, a certain level of dynamics needs to be conserved for an adaptive interface toward the living environment. A balance between robust material functionalization and dynamic cell interaction needs to be met. The detailed analysis hereof using a ureido‐pyrimidinone (UPy) poly(ethylene glycol) system in dilute and transient network regime is demonstrated. Monovalent and bivalent UPy‐functionalized guest molecules are designed and their interaction with UPy‐host fibers is evaluated. Analysis of guest interaction in the dilute state by microfluidics, and in the gel state, by fluorescence recovery after photobleaching and fluorescence resonance energy transfer is proven to be suitable to quantify the local and ensemble guest mobility. The results demonstrate that the interaction of bioactive moieties through supramolecular host–guest chemistry yields a dynamic system, which is stronger for divalent guests but risks unintended leakage in the case of functional monomeric units. 相似文献
10.
Bastian Rsch Thomas Xaver Gentner Holger Elsen Christian A. Fischer Jens Langer Michael Wiesinger Sjoerd Harder 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(16):5450-5455
Key to the isolation of the first alkyl strontium complex was the synthesis of a strontium hydride complex that is stable towards ligand exchange reactions. This goal was achieved by using the super bulky β‐diketiminate ligand DIPePBDI (CH[C(Me)N‐DIPeP]2, DIPeP=2,6‐diisopentylphenyl). Reaction of DIPePBDI‐H with Sr[N(SiMe3)2]2 gave (DIPePBDI)SrN(SiMe3)2, which was converted with PhSiH3 into [(DIPePBDI)SrH]2. Dissolved in C6D6, the strontium hydride complex is stable up to 70 °C. At 60 °C, H–D isotope exchange gave full conversion into [(DIPePBDI)SrD]2 and C6D5H. Since H–D exchange with D2 is facile, the strontium hydride complex served as a catalyst for the deuteration of C6H6 by D2. Reaction of [(DIPePBDI)SrH]2 with ethylene gave [(DIPePBDI)SrEt]2. The high reactivity of this alkyl strontium complex is demonstrated by facile ethylene polymerization and nucleophilic aromatic substitution with C6D6, giving alkylated aromatic products and [(DIPePBDI)SrD]2. 相似文献