全文获取类型
收费全文 | 2713篇 |
免费 | 58篇 |
国内免费 | 10篇 |
专业分类
化学 | 2003篇 |
晶体学 | 38篇 |
力学 | 60篇 |
数学 | 331篇 |
物理学 | 349篇 |
出版年
2022年 | 35篇 |
2021年 | 25篇 |
2020年 | 43篇 |
2019年 | 30篇 |
2018年 | 19篇 |
2017年 | 24篇 |
2016年 | 43篇 |
2015年 | 46篇 |
2014年 | 57篇 |
2013年 | 131篇 |
2012年 | 126篇 |
2011年 | 172篇 |
2010年 | 92篇 |
2009年 | 66篇 |
2008年 | 147篇 |
2007年 | 165篇 |
2006年 | 149篇 |
2005年 | 164篇 |
2004年 | 144篇 |
2003年 | 109篇 |
2002年 | 113篇 |
2001年 | 43篇 |
2000年 | 26篇 |
1999年 | 31篇 |
1998年 | 31篇 |
1997年 | 29篇 |
1996年 | 41篇 |
1995年 | 22篇 |
1994年 | 23篇 |
1993年 | 28篇 |
1992年 | 26篇 |
1991年 | 34篇 |
1990年 | 24篇 |
1989年 | 15篇 |
1988年 | 27篇 |
1987年 | 17篇 |
1986年 | 19篇 |
1985年 | 27篇 |
1984年 | 33篇 |
1983年 | 19篇 |
1982年 | 33篇 |
1981年 | 23篇 |
1980年 | 17篇 |
1979年 | 26篇 |
1978年 | 20篇 |
1977年 | 23篇 |
1976年 | 22篇 |
1975年 | 18篇 |
1974年 | 20篇 |
1973年 | 18篇 |
排序方式: 共有2781条查询结果,搜索用时 15 毫秒
111.
112.
113.
Cai QJ Chan-Park MB Lu ZS Li CM Ong BS 《Langmuir : the ACS journal of surfaces and colloids》2008,24(20):11889-11894
A series of alkanethiol monolayers (CH 3(CH 2) n-1 SH, n = 4, 6, 8, 10, 12, 14, 16) were used to modify gold source-drain electrode surfaces for bottom-contact poly(3,3'-didodecylquaterthiophene) (PQT-12) thin-film transistors (TFTs). The device mobilities of TFTs were significantly increased from approximately 0.015 cm (2) V (-1) s (-1) for bare electrode TFTs to a maximum of approximately 0.1 cm (2) V (-1) s (-1) for the n = 8 monolayer devices. The mobilities of devices with alkanethiol-modified Au electrodes varied parabolically with alkyl length with values of 0.06, 0.1, and 0.04 cm (2) V (-1) s (-1) at n = 4, 8, and 16, respectively. Atomic force microscopy investigations reveal that alkanethiol electrode surface modifications promote polycrystalline PQT-12 morphologies at electrode/PQT-12 contacts, which probably increase the density of states of the PQT-12 semiconductor at the interfaces. The contact resistance of TFTs is strongly modulated by the surface modification and strongly varies with the alkanethiol chain length. The surface modifications of electrodes appear to significantly improve the charge injection, with consequent substantial improvement in device performance. 相似文献
114.
Zhang C Occi J Masurekar P Barrett JF Zink DL Smith S Onishi R Ha S Salazar O Genilloud O Basilio A Vicente F Gill C Hickey EJ Dorso K Motyl M Singh SB 《Journal of the American Chemical Society》2008,130(36):12102-12110
Bacterial resistance to antibiotics, particularly to multiple drug resistant antibiotics, is becoming cause for significant concern. The only really viable course of action is to discover new antibiotics with novel mode of actions. Thiazolyl peptides are a class of natural products that are architecturally complex potent antibiotics but generally suffer from poor solubility and pharmaceutical properties. To discover new thiazolyl peptides potentially with better desired properties, we designed a highly specific assay with a pair of thiazomycin sensitive and resistant strains of Staphylococcus aureus, which led to the discovery of philipimycin, a new thiazolyl peptide glycoside. It was isolated along with an acid-catalyzed degradation product by bioassay-guided fractionation. Structure of both compounds was elucidated by extensive application of 2D NMR, 1D TOCSY, and HRESIFT-MS/MS. Both compounds showed strong antibacterial activities against gram-positive bacteria including MRSA and exhibited MIC values ranging from 0.015 to 1 microg/mL. Philipimycin was significantly more potent than the degradation product. Both compounds showed selective inhibition of protein synthesis, indicating that they targeted the ribosome. Philipimycin was effective in vivo in a mouse model of S. aureus infection exhibiting an ED50 value of 8.4 mg/kg. The docking studies of philipimycin suggested that a part of the molecule interacts with the ribosome and another part with Pro23, Pro22, and Pro26 of L11 protein, which helped in explaining the differential of activities between the sensitive and resistant strains. The design and execution of the bioassay, the isolation, structure, in vitro and in vivo antibacterial activity, and docking studies of philipimycin and its degradation product are described. 相似文献
115.
The selective preconcentration of estradiol was explored using the recognition ability of a molecularly imprinted polymer (MIP) in the solid phase extraction (SPE) format. Polymeric particles were imprinted with 17β-estradiol using methacrylic acid as functional monomer and divinylbenzene as crosslinker. Binding studies of these polymeric particles towards 17β-estradiol showed selectivity over non-imprinted polymers, using acetonitrile as solvent. The imprinted polymer showed a recovery of 88% for β-estradiol in deionized water and 81% in surface water. The selectivity of the MIP over the non-imprinted polymer was relatively low, only 10% higher recovery. The results indicate that the MIP imprinted with 17β-estradiol does not appear to provide a viable approach to be used in a sample clean-up or enrichment step for the determination of estradiol in aqueous systems. 相似文献
116.
Kaltgrad E O'Reilly MK Liao L Han S Paulson JC Finn MG 《Journal of the American Chemical Society》2008,130(14):4578-4579
Glycans arrayed on the exterior of virus particles were used as substrates for glycosyltransferase reactions to build di- and trisaccharides from the virus surface. The resulting particles exhibited tight and specific associations with cognate receptors on beads and cells, in one example defeating in cis cell-surface interactions in a manner characteristic of polyvalent binding. Combined with the ability of viruses to provide structurally well-defined attachment points, the methodology provides a convenient and powerful way to prepare complex carbohydrate ligands for clustered receptors. 相似文献
117.
Very high order open-shell Z-averaged perturbation theory (ZAPT) energies, equilibrium bond lengths, and harmonic vibrational frequencies have been computed for a suite of small molecules using a determinantal algorithm. The convergence of ZAPTn energies is compared to alternative Moller-Plesset (MP) perturbation theories built on restricted open-shell Hartree-Fock (ROMP, RMP, OPT1, and OPT2) and unrestricted Hartree-Fock (UMP) reference wave functions for NH(2) at three N-H bond lengths and for CN. The ZAPTn energy series closely parallel those of RMPn and ROMPn theories for these systems. Further, we examine the convergence of ZAPTn energies, equilibrium bond lengths (r(e)), and harmonic vibrational frequencies (omega(e)) for X (2)Sigma(g)(+) CN, X (4)Sigma(g) (-) C(2)(+), and b (2)Delta(g) C(2)(+), tracking oscillations in the energy series for the challenging latter system to order 1000. Finally, we obtain r(e) and omega(e) values from explicit ZAPT2 and ZAPT4 computations with a triple-zeta plus double polarization basis set. The ensuing results are very close to those from second- and fourth-order RMP and ROMP for the NO and CN molecules but are significantly closer to experiment in the case of (3)Sigma(g)(-) O(2). The ZAPTn series exhibit all the fascinating diversity of behavior previously observed for closed-shell MPn theory. Particularly encouraging is the ability of Feenberg transformations to remove erratic, strongly oscillatory, and divergent behavior that may occur in ZAPTn series and provide systematic improvements toward the full configuration interaction limit. In light of the appealing mathematical properties of ZAPT and similarity of results to those from the oft-applied RMP theory, coupled with the reductions in computational cost inherent in the ZAPT method relative to theories requiring different orbitals for different spins, we recommend low-order ZAPT for general applications to open-shell systems, particularly in cases where spin contamination is of concern. 相似文献
118.
Tyler R. Priddy-Arrington Reagan E. Edwards Claire E. Colley Marissa M. Nguyen Tess Hamilton-Adaire Mary E. Caldorera-Moore 《Macromolecular bioscience》2023,23(6):2200505
In recent years, there has been an increased interest in injectable, in situ crosslinking hydrogels due to their minimally invasive application and ability to conform to their environment. Current in situ crosslinking chitosan hydrogels are either mechanically robust with poor biocompatibility and limited biodegradation due to toxic crosslinking agents or the hydrogels are mechanically weak and undergo biodegradation too rapidly due to insufficient crosslinking. Herein, the authors developed and characterized a thermally-driven, injectable chitosan-genipin hydrogel capable of in situ crosslinking at 37 °C that is mechanically robust, biodegradable, and maintain high biocompatibility. The natural crosslinker genipin is utilized as a thermally-driven, non-toxic crosslinking agent. The chitosan-genipin hydrogel's crosslinking kinetics, injectability, viscoelasticity, swelling and pH response, and biocompatibility against human keratinocyte cells are characterized. The developed chitosan-genipin hydrogels are successfully crosslinked at 37 °C, demonstrating temperature sensitivity. The hydrogels maintained a high percentage of swelling over several weeks before degrading in biologically relevant environments, demonstrating mechanical stability while remaining biodegradable. Long-term cell viability studies demonstrated that chitosan-genipin hydrogels have excellent biocompatibility over 7 days, including during the hydrogel crosslinking phase. Overall, these findings support the development of an injectable, in situ crosslinking chitosan-genipin hydrogel for minimally invasive biomedical applications. 相似文献
119.
The anisotropic elastic constants of crystalline octacyclopentyl polyhedral oligomeric silsesquioxane (CpPOSS) were determined using molecular dynamics. The force field used for these calculations was shown to model accurately the rhombohedral and triclinic crystal structures of octasilsesquioxane and CpPOSS, respectively, as well as the vibrational frequencies of octasilsesquioxane. The moduli for CpPOSS are anisotropic, with a Reuss-averaged bulk modulus of 7.5 GPa, an isotropic averaged Young's modulus of 11.78 GPa, and an isotropic averaged shear modulus of 4.75 GPa. These isotropic averages or, alternatively, the full anisotropic stiffness tensor of the crystal can be used with micromechanical composite models to calculate the effective elastic properties of polymer nanocomposites that contain crystalline aggregates of CpPOSS. 相似文献
120.
Jiang H Li Y Pelzer M Cannon MJ Randlett C Junga H Jiang X Ji QC 《Journal of chromatography. A》2008,1192(2):230-238
A sensitive and selective bioanalytical assay was developed and validated for the determination of enantiomeric molindone in human plasma using high-performance liquid chromatography-tandem mass spectrometry along with supported liquid extraction procedures. The chiral separation was evaluated and optimized on macrocyclic antibiotic type chiral stationary phases (CSPs) based on teicoplanin aglycone (Chirobiotic TAG) in polar organic, polar ionic, and reversed-phase mode chromatography, respectively. Complete baseline separation was achieved on a Chirobiotic TAG column under isocratic condition in reversed-phase chromatography. The method validation was conducted using a Chirobiotic TAG column (100 mm x 2.1 mm) over the curve range 0.100-100 ng/ml for each molindone enantiomer using 0.0500 ml of plasma sample. The flow rate was 0.8 ml/min and the total run time was 9 min. Supported liquid extraction in a 96-well plate format was used for sample preparation. Parameters including recovery, matrix effect, linearity, sensitivity, specificity, carryover, precision, accuracy, dilution integrity, and stability were evaluated. The intra- and inter-day precision and accuracy of the quality control samples at low, medium, and high concentration levels were RSD 相似文献