全文获取类型
收费全文 | 3893篇 |
免费 | 125篇 |
国内免费 | 23篇 |
专业分类
化学 | 2848篇 |
晶体学 | 42篇 |
力学 | 105篇 |
数学 | 477篇 |
物理学 | 569篇 |
出版年
2023年 | 17篇 |
2022年 | 18篇 |
2021年 | 37篇 |
2020年 | 59篇 |
2019年 | 54篇 |
2018年 | 49篇 |
2017年 | 37篇 |
2016年 | 106篇 |
2015年 | 83篇 |
2014年 | 87篇 |
2013年 | 212篇 |
2012年 | 254篇 |
2011年 | 293篇 |
2010年 | 118篇 |
2009年 | 107篇 |
2008年 | 271篇 |
2007年 | 290篇 |
2006年 | 271篇 |
2005年 | 266篇 |
2004年 | 189篇 |
2003年 | 170篇 |
2002年 | 151篇 |
2001年 | 52篇 |
2000年 | 54篇 |
1999年 | 38篇 |
1998年 | 40篇 |
1997年 | 43篇 |
1996年 | 58篇 |
1995年 | 35篇 |
1994年 | 41篇 |
1993年 | 29篇 |
1992年 | 34篇 |
1991年 | 31篇 |
1990年 | 38篇 |
1989年 | 24篇 |
1988年 | 20篇 |
1987年 | 12篇 |
1986年 | 18篇 |
1985年 | 25篇 |
1984年 | 41篇 |
1983年 | 30篇 |
1982年 | 38篇 |
1981年 | 31篇 |
1980年 | 22篇 |
1979年 | 17篇 |
1978年 | 25篇 |
1977年 | 16篇 |
1976年 | 14篇 |
1974年 | 17篇 |
1973年 | 12篇 |
排序方式: 共有4041条查询结果,搜索用时 15 毫秒
981.
982.
Arvind Kumar Michael A. Invernale Sung‐Yeon Jang Gregory A. Sotzing 《Journal of polymer science. Part A, Polymer chemistry》2010,48(4):756-763
Herein, we report the synthesis of conducting poly (terthiophene)s using a side chain precursor polymer approach. Random copolymers were prepared by ring opening metathesis polymerization of two norbornylene monomers, one containing a pendant terthiophene group and the other containing a pendant acetate group. Solid‐state oxidative conversion of the terthiophene units was used to produce conductive polymers. Oxidative solid‐state conversion was successful for copolymers containing as little as 1 mol % of terthiophene comonomer. The electrical and optical properties of CPs were studied as a function of the amount of electroactive moiety, terthiophene (3T), present in the copolymer. The CPs were found to have conductivity varying between 10?1 and 10?4 S/cm depending on the precursor copolymer compositions. The CPs obtained from all precursors had no significant difference in their energy gaps and showed blue to orange color transitions when switching from the oxidized to the neutral states, respectively. The absorbance intensity at 426 nm for poly(3T) from the precursors fits the Beer–Lambert law corresponding to the range of initial 3T content in the precursor copolymer composition (from 1 to 100 mol %). © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 756–763, 2010 相似文献
983.
Debopreeti Mukherjee Pablo Trigo-Mouriño Yuan Jiang Timothy Nowak Vladimir Shchurik Donovon A. Adpressa Michael T. Louie Shane R. Reynolds Michael J. Hohn Mohammad Ahmed Al-Sayah Gregory F. Pirrone Alexey A. Makarov 《Journal of separation science》2022,45(12):2055-2063
Recent advances in the field of cancer biology have accelerated the discovery and development of novel biopharmaceuticals. At the forefront of these drug development efforts are high-throughput screening, compressed timelines, and limited sample quantities, all characteristic of the discovery space. To meet program targets, large numbers of protein variants must be produced, screened, and characterized, presenting a daunting analytical challenge. Additionally, the higher-order structure is paramount for protein function and must be monitored as a critical quality attribute. Matrix-assisted laser desorption/ionization mass spectrometry has been utilized as an ultra-fast, automatable, sample-sparing analytical tool for biomolecules. Our group has published applications integrating hydrogen-deuterium exchange mass spectrometry with matrix-assisted laser desorption/ionization mass spectrometry for the rapid conformational characterization of small proteins, the current work expands this application to monoclonal and bi-specific antibodies. This study demonstrates the ability of the methodology, matrix-assisted laser desorption/ionization hydrogen-deuterium exchange mass spectrometry, to detect conformational differences between bi-specific antibodies from different expression hosts. These conformational differences were validated by orthogonal techniques including circular dichroism, nuclear magnetic resonance, and size-exclusion chromatography hydrogen-deuterium exchange mass spectrometry. This work demonstrates the utility of applying the developed methodology as a rapid conformational screening tool to triage samples for further analytical characterization. 相似文献
984.
985.
Emily Kerr Egan H. Doeven Gregory J. Barbante Conor F. Hogan David J. Bower Paul S. Donnelly Timothy U. Connell Paul S. Francis 《Chemical science》2015,6(1):472-479
We demonstrate the mixed annihilation electrogenerated chemiluminescence of tris(2,2′-bipyridine)ruthenium(ii) with various cyclometalated iridium(iii) chelates. Compared to mixed ECL systems comprising organic luminophores, the absence of T-route pathways enables effective predictions of the observed ECL based on simple estimations of the exergonicity of the reactions leading to excited state production. Moreover, the multiple, closely spaced reductions and oxidations of the metal chelates provide the ability to finely tune the energetics and therefore the observed emission colour. Distinct emissions from multiple luminophores in the same solution are observed in numerous systems. The relative intensity of these emissions and the overall emission colour are dependent on the particular oxidized and reduced species selected by the applied electrochemical potentials. Finally, these studies offer insights into the importance of electronic factors in the question of whether the reduced or oxidized partner becomes excited in annihilation ECL. 相似文献
986.
Lauren R. Holloway Michael C. Young Gregory J. O. Beran Richard J. Hooley 《Chemical science》2015,6(8):4801-4806
Subtle differences in ligand coordination angle and rigidity lead to high fidelity sorting between individual components displaying identical coordination motifs upon metal-mediated self-assembly. Narcissistic self-sorting can be achieved between highly similar ligands that vary minimally in rigidity and internal coordination angle upon combination with Fe(ii) ions and 2-formylpyridine. Selective, sequential cage formation can be precisely controlled in a single flask from a mix of three different core ligands (and 33 total components) differing only in the hybridization of one group that is uninvolved in the metal coordination process. 相似文献
987.
Shelbi Parker Radu Reit Haley Abitz Gregory Ellson Kejia Yang Benjamin Lund Walter E. Voit 《Macromolecular rapid communications》2016,37(13):1027-1032
Thiol‐click reactions lead to polymeric materials with a wide range of interesting mechanical, electrical, and optical properties. However, this reaction mechanism typically results in bulk materials with a low glass transition temperature (Tg) due to rotational flexibility around the thioether linkages found in networks such as thiol‐ene, thiol‐epoxy, and thiol‐acrylate systems. This report explores the thiol‐maleimide reaction utilized for the first time as a solvent‐free reaction system to synthesize high‐Tg thermosetting networks. Through thermomechanical characterization via dynamic mechanical analysis, the homogeneity and Tgs of thiol‐maleimide networks are compared to similarly structured thiol‐ene and thiol‐epoxy networks. While preliminary data show more heterogeneous networks for thiol‐maleimide systems, bulk materials exhibit Tgs 80 °C higher than other thiol‐click systems explored herein. Finally, hollow tubes are synthesized using each thiol‐click reaction mechanism and employed in low‐ and high‐temperature environments, demonstrating the ability to withstand a compressive radial 100 N deformation at 100 °C wherein other thiol‐click systems fail mechanically.
988.
Gregory J. Puleo 《Journal of Graph Theory》2015,80(1):12-17
Erd?s, Gallai, and Tuza posed the following problem: given an n‐vertex graph G, let denote the smallest size of a set of edges whose deletion makes G triangle‐free, and let denote the largest size of a set of edges containing at most one edge from each triangle of G. Is it always the case that ? We have two main results. We first obtain the upper bound , as a partial result toward the Erd?s–Gallai–Tuza conjecture. We also show that always , where m is the number of edges in G; this bound is sharp in several notable cases. 相似文献
989.
Golas PL Louie S Lowry GV Matyjaszewski K Tilton RD 《Langmuir : the ACS journal of surfaces and colloids》2010,26(22):16890-16900
A series of polyelectrolytes with controlled molecular weight, a narrow chain-length distribution, and systematic structural differences were synthesized using atom-transfer radical polymerization and investigated as stabilizers for magnetite nanoparticles in aqueous suspensions. Structural differences include the degree of polymerization, the chain architecture, and the identity of the charged functional unit. The synthesized polymers are sulfonated poly(2-hydroxyethyl methacrylate), a block copolymer of the former with poly(n-butyl methacrylate), poly(sodium styrene sulfonate), poly(sodium acrylate), and poly(sodium vinylphosphonate). The colloidal stability is assessed by measuring the fraction of particles, based on turbidity, that sediment after a period of time at increasing ionic strength. Sedimentation results are complimented by dynamic light scattering determinations of the hydrodynamic diameter of the particles that remain suspended. When adsorption and sedimentation are conducted at high pH, poly(sodium acrylate) and poly(sodium vinylphosphonate) yield the most stable suspensions because of their strong coordinative interactions with the iron oxide surface. At low pH, the polymers that retain pendant negative charges (each of the sulfonated polymers) yield high stable fractions at all ionic strengths investigated up to 100 mM (NaCl), whereas polyelectrolytes that become protonated with decreasing pH, poly(sodium acrylate) and poly(sodium vinylphosphonate), lose their stabilizing capacity even at low ionic strengths. The chain-length distribution profoundly alters a polymer's stabilization tendencies. Two poly(sodium acrylate) samples with the same number-average molecular weight but widely different chain-length distributions proved to have opposite tendencies, with the polydisperse sample being a good stabilizer and the low polydispersity one being a strong flocculant. This investigation provides guidelines for the design of polymeric stabilizers for magnetite nanoparticles according to the pH and ionic strength of the intended application. 相似文献
990.
Agrawal SK Sanabria-DeLong N Bhatia SK Tew GN Bhatia SR 《Langmuir : the ACS journal of surfaces and colloids》2010,26(22):17330-17338
We report the energetics of association in polymeric gels with two types of junction points: crystalline hydrophobic junctions and polymer-nanoparticle junctions. Time-temperature superposition (TTS) of small-amplitude oscillatory rheological measurements was used to probe crystalline poly(L-lactide) (PLLA)-based gels with and without added laponite nanoparticles. For associative polymer gels, the activation energy derived from the TTS shift factors is generally accepted as the associative strength or energy needed to break a junction point. Our systems were found to obey TTS over a wide temperature range of 15-70 °C. For systems with no added nanoparticles, two distinct behaviors were seen, with a transition occurring at a temperature close to the glass transition temperature of PLLA, T(g). Above T(g), the activation energy was similar to the PLLA crystallization enthalpy, suggesting that the activation energy is related to the energy needed to pull a PLLA chain out of the crystalline domain. Below T(g), the activation energy is expected to be the energy required to increase mobility of the polymer chains and soften the glassy regions of the PLLA core. Similar behavior was seen in the nanocomposite gels with added laponite; however, the added clay appears to reduce the average value of the activation enthalpy. This confirms our SAXS results and suggests that laponite particles are participating in the network structure. 相似文献