全文获取类型
收费全文 | 283篇 |
免费 | 20篇 |
专业分类
化学 | 223篇 |
晶体学 | 1篇 |
力学 | 7篇 |
数学 | 16篇 |
物理学 | 56篇 |
出版年
2023年 | 2篇 |
2021年 | 4篇 |
2020年 | 8篇 |
2019年 | 7篇 |
2018年 | 3篇 |
2017年 | 2篇 |
2016年 | 8篇 |
2015年 | 6篇 |
2014年 | 12篇 |
2013年 | 6篇 |
2012年 | 19篇 |
2011年 | 19篇 |
2010年 | 10篇 |
2009年 | 7篇 |
2008年 | 15篇 |
2007年 | 14篇 |
2006年 | 24篇 |
2005年 | 14篇 |
2004年 | 13篇 |
2003年 | 10篇 |
2002年 | 17篇 |
2001年 | 8篇 |
2000年 | 10篇 |
1999年 | 5篇 |
1998年 | 1篇 |
1997年 | 2篇 |
1996年 | 6篇 |
1995年 | 2篇 |
1994年 | 9篇 |
1993年 | 3篇 |
1992年 | 2篇 |
1991年 | 6篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 3篇 |
1984年 | 5篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1981年 | 2篇 |
1980年 | 1篇 |
1978年 | 2篇 |
1975年 | 2篇 |
1973年 | 2篇 |
1972年 | 1篇 |
1971年 | 1篇 |
1970年 | 2篇 |
排序方式: 共有303条查询结果,搜索用时 31 毫秒
81.
High-power single-polarization and single-transverse-mode fiber laser with an all-fiber cavity and fiber-grating stabilized spectrum 总被引:1,自引:0,他引:1
Liu CH Galvanauskas A Khitrov V Samson B Manyam U Tankala K Machewirth D Heinemann S 《Optics letters》2006,31(1):17-19
Conventionally, large-mode-area (LMA) fiber lasers use free-space polarizing components to achieve linear polarization output. External components, however, significantly limit laser robustness and power scalability. We demonstrate, to the best of our knowledge, the first high-power all-fiber cavity single-polarization single-transverse-mode LMA fiber laser, without the use of free-space polarizing components. This has been achieved by using tightly coiled high-birefringence 20 microm core LMA fiber. The lasing spectrum at 1085 nm has been stabilized by a fiber grating, spliced at one end of a LMA fiber. Up to 405 W of single-polarization output with a polarization extinction of >19 dB with a narrow spectrum (1.9 nm FWHM) and in a single-transverse mode (M2 < 1.1) has been demonstrated. The simplicity of a monolithic-cavity approach is highly beneficial for a number of applications, including the use of a fiber laser for nonlinear wavelength conversion and for coherent and spectral beam combining. 相似文献
82.
1,5-Di(hetero)arylated-pyridin-2(1H)-one derivatives have been readily obtained in good yields starting from 2-fluoro-5-pyridylboronic acid. The sequence comprises three steps: (i) palladium-catalysed Suzuki-Miyaura reaction; (ii) base-catalysed hydrolysis; (iii) copper-catalysed C-N coupling. X-ray crystal structures are reported for selected pyridin-2(1H)-one derivatives. These compounds are of interest as new scaffolds for drug discovery. 相似文献
83.
84.
Alves GA Amato S Anjos JC Appel JA Astorga J Bernard T Bracker SB Cremaldi LM Darling CL Dixon RL Errede D Gay C Green DR Jedicke R Karchin PE Kwan S Lueking LJ de Mello Neto JR Metheny J Milburn RH de Miranda JM da Motta Filho H Napier A Passmore D Rafatian A dos Reis AC Ross WR Santoro AF Sheaff M Souza MH Spalding WJ Stoughton C Streetman ME Summers DJ Takach SF Wallace A Wu Z 《Physical review letters》1994,72(6):812-815
85.
86.
P.D. Collier T. Bryce R. Mallows P.E. Thomas D.J. Frost O. Korver C.K. Wilkins 《Tetrahedron》1973,29(1):125-142
The structures, relative configurations and precursors of seven pigments isolated from the theaflavin fraction of black tea have been established by synthesis, and by NMR and mass spectrometry. The four principal pigments are the bis-flavan-substituted 1′,2′-dihydroxy-3,4-benzotropolones theaflavin, the corresponding isomeric 3- and 3′-monogallates, and the 3,3′-digallate. Collapsed spin-spin couplings and nuclear Overhauser effects in these and a range of mono-flavan-substituted model compounds are interpreted in terms of steric hindrance to rotation of flavan groups with respect to the benzotropolone ring. As a result of these steric effects, the 3-gallate and 3,3′-digallate exist in rotameric forms which are clearly distinguished in the temperature-dependent CD spectra. 相似文献
87.
Model studies of colloidal silica precipitation using biosilica extracts from<Emphasis Type="Italic"> Equisetum telmateia</Emphasis> 总被引:1,自引:0,他引:1
Structural materials containing silicon are produced in single celled organisms through to higher plants and animals. Hydrated amorphous silica is a colloidal mineral of infinite functionality that is formed into structures with microscopic and macroscopic form. Proteins and proteoglycans are suggested to play a critical role in the catalysis of silica polycondensation and in structure direction during the formation of these magnificent structures. This article extends knowledge on the effect of protein containing biosilica extracts from Equisetum telmateia on the kinetics of silica formation and structure regulation. Utilising potassium silicon catecholate as the source of soluble silicon, bioextracts obtained from plant silica by dissolution of the siliceous phase with aqueous HF following extensive acid digestion of the plant cell wall were found to modify the kinetic rate constants for the formation of small silicic acid oligomers under circumneutral pH conditions and to modify the solubility of silicic acid in solution. Addition of the bioextracts at ca. 1 wt% to the reaction medium reduced the sizes and range of sizes of the fundamental silica particles formed and led to the formation of crystalline polymorphs of silica under conditions of ca. neutral pH, room temperature and in the absence of multiply charged cations, conditions assumed to be relevant to the biological mineralization environment. The ability of biological organisms to regulate the formation of silica structures with prevention of crystallinity is discussed as are the implications of this study in terms of the generation of new materials with specific form and function for industrial application. 相似文献
88.
Periodic trends in indirect nuclear spin-spin coupling tensors: relativistic density functional calculations for interhalogen diatomics 总被引:2,自引:0,他引:2
Bryce DL Wasylishen RE Autschbach J Ziegler T 《Journal of the American Chemical Society》2002,124(17):4894-4900
There have been significant advances in the calculation and interpretation of indirect nuclear spin-spin coupling (J) tensors during the past few years; however, much work remains to be done, especially for molecules containing heavy atoms where relativistic effects may play an important role. Many J tensors cannot be explained based solely on a nonrelativistic Fermi-contact mechanism. In the present work, the relativistic zeroth-order regular approximation density-functional (ZORA-DFT) implementation for the calculation of J has been applied to the complete series of homonuclear and heteronuclear diatomic halogen molecules: F(2), Cl(2), Br(2), I(2), At(2), ClF, BrF, IF, ClBr, ClI, and BrI. For all of these compounds, the reduced isotropic coupling constant (K(iso)) is positive and the reduced anisotropic coupling constant (DeltaK) is negative. With the exception of molecular fluorine, the magnitudes of K(iso) and DeltaK are shown to increase linearly with the product of the atomic numbers of the coupled nuclei. ZORA-DFT calculations of J for F(2) and ClF are in excellent agreement with the results obtained from multiconfigurational self-consistent-field calculations. The relative importance of the various coupling mechanisms is approximately constant for all of the compounds, with the paramagnetic spin-orbit term being the dominant contributor to K(iso), at approximately 70-80%. Available experimental stimulated resonant Raman spectroscopy data are exploited to extract the complete J((127)I,(127)I) tensor for iodine in two rotational states. The dependence of K(iso) and DeltaK on bond length and rovibrational state is investigated by using calculated results in combination with available experimental data. In addition to providing new insights into periodic trends for J coupling tensors, this work further demonstrates the utility of the ZORA-DFT method and emphasizes the necessity of spin-orbit relativistic corrections for J calculations involving heavy nuclei. 相似文献
89.
Jones AE Christensen CA Perepichka DF Batsanov AS Beeby A Low PJ Bryce MR Parker AW 《Chemistry (Weinheim an der Bergstrasse, Germany)》2001,7(5):973-978
Flash photolysis of bis[4.5-di(methylsulfanyl) 1,3-dithiol-2-ylidene]-9,10(-dihydroanthracene (1) in chloroform leads to formation of the transient radical cation species 1.+ which has a diagnostic broad absorption band at lambdamax approximately 650 nm. This band decays to half its original intensity over a period of about 80 micros. Species 1.+ has also been characterised by resonance Raman spectroscopy. In degassed solution 1.+ disproportionates to give the dication 1(2+), whereas in aerated solutions the photodegradation product is the 10-[4,5-di(methylsulfanyl) 1,3-dithiol-2-ylidene]anthracene-9(10 H)one (2). The dication 1(2+) has been characterised by a spectroelectrochemical study [lambdamax (CH2Cl2) = 377, 392, 419, 479 nm] and by an X-ray crystal structure of the salt 1(2-) (ClO4)2, which was obtained by electrocrystallisation. The planar anthracene and 1,3-dithiolium rings in the dication form a dihedral angle of 77.2 degrees; this conformation is strikingly different from the saddle-shaped structure of neutral 1 reported previously. 相似文献
90.
Qualitative characterization of the diffusion of cationic-modified PVA into the cellulose fiber pores 总被引:1,自引:0,他引:1
Pedram Fatehi Bryce MacMillan Zainab Ziaee Huining Xiao 《Colloids and surfaces. A, Physicochemical and engineering aspects》2009,348(1-3):59-63
In this work, the diffusion of cationic poly (vinyl alcohol) (CPVA) with well-defined structures into the pores of bleached kraft fibers was investigated at equilibrium level of adsorption by means of adsorption, solute exclusion technique (SET), and nuclear magnetic resonance (NMR) relaxation method. The results showed that the interaction between CPVA and dextran polymers was weak, which allowed us to use the SET method to investigate the variation in the pore size of fibers upon diffusing CPVAs. Both adsorption and SET methods confirmed the diffusion of CPVA polymers into the fiber pores. However, the NMR technique was unable to reflect the pore size changes. The main reason for such results was probably the error that occurred in removing water between fibers via applying the water retention value (WRV) test prior to the NMR analysis. In fact, not all of the water on the fiber surface, especially on the surface of CPVA-modified fibers, could be removed by the WRV, introducing some error in the NMR analysis. 相似文献