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61.
Leanne G. Bloor Claire J. Carmalt David Pugh 《Coordination chemistry reviews》2011,255(11-12):1293-1318
Gallium and indium oxide thin films have received much attention in recent years for their wide range of applications. This review summarises the literature concerning single-source precursors and the methods employed to deposit gallium and indium oxide thin films using these compounds. An update of the literature outlining compounds which are potential single-source precursors to these materials is also included. 相似文献
62.
Leanne Rylands Vilma Simbag Kelly E. Matthews Carmel Coady Shaun Belward 《International Journal of Mathematical Education in Science & Technology》2013,44(6):834-845
There is general agreement in Australia and beyond that quantitative skills (QS) in science, the ability to use mathematics and statistics in context, are important for science. QS in the life sciences are becoming ever more important as these sciences become more quantitative. Consequently, undergraduates studying the life sciences require better QS than at any time in the past. Ways in which mathematics and science academics are working together to build the QS of their undergraduate science students, together with the mathematics and statistics needed or desired in a science degree, are reported on in this paper. The emphasis is on the life sciences. Forty-eight academics from eleven Australian and two USA universities were interviewed about QS in science. Information is presented on: what QS academics want in their undergraduate science students; who is teaching QS; how mathematics and science departments work together to build QS in science and implications for building the QS of science students. This information leads to suggestions for improvement in QS within a science curriculum. 相似文献
63.
Angular distribution measurements of reactive scattering of a supersonic potassium atom beam by a series of molecules are reported with initial kinetic energy (~ 5 kcal mole-1) above the thermal energy range. The narrow Laval nozzle velocity distribution gives improved resolution over thermal energy measurements. Total reaction cross sections are found to decrease with energy. Differential reaction cross sections for Br2, BrCN and CCl4 show increased forward scattering compared with thermal energies but for CH3I there is no change to within experimental error. The BrCN scattering is compatible with spectator-stripping dynamics, though this limit has not been reached in the Br2 scattering. The SnCl4 differential reaction cross section appears not to be compatible with a single peak in the centre of mass recoil velocity distribution. It is suggested that high and low velocity contributions to the intensity may arise from a long-lived collision complex dissociating by two reaction paths. 相似文献
64.
Angular distribution measurements of KX reactive scattering of a potassium dimer K2 beam by mercuric halide molecules HgX2 are reported. All the reactions exhibit strong forward peaking in the centre of mass differential cross sections and large total reaction cross sections Qr ~ 150 Å2. However, there is substantial backward peaking ( forward peak) for HgBr2, HgI2. Despite the direct stripping dynamics, both alkali atoms of the K2 dimer become bound alkali halide molecules in most (perhaps all) reactive collisions. A major fraction of the reaction exoergicity is disposed into vibrational excitation of the product KX molecules. A mechanism involving a first electron jump in the entrance valley and a second electron jump in the exit valley of the potential surface is suggested to explain the rapid transfer of both K2 valence electrons. 相似文献
65.
Isotope‐labeled differential profiling of metabolites using N‐benzoyloxysuccinimide derivatization coupled to liquid chromatography/high‐resolution tandem mass spectrometry 下载免费PDF全文
66.
Brominated furanones have attracted recent interest as antibacterial compounds. To utilize them as protective coatings in biomedical device applications, they must be covalently immobilized onto solid surfaces; however, interfacial coupling protocols developed for other biomolecules are not applicable to furanones. An azide reaction scheme has enabled covalent immobilization onto fluorinated ethylene propylene copolymer but its chemistry is less predictable, requiring detailed characterization by XPS and tapping mode AFM after each step of the immobilization sequence. XPS curve fitting resolved components in the C 1s, N 1s and Br 3d regions. Angle dependent XPS was used to assess the depth distributions and layer thicknesses. The results indicated successful covalent immobilization of furanones; however, side reactions occurred. In addition to the expected CBr, a contribution from bromine ion (Br−) was detected, indicating that photo-degradation of furanones took place during UV illumination, and this reaction was found to increase with illumination time. The Br− was removed by washing with water, whereas the CBr signal from immobilized furanone remained. Spectroscopic characterization will assist in elucidating the structure of furanone coatings, understanding their mode of action when covalently immobilized on surfaces, and rationally designing and optimizing an effective antibacterial coating for biomedical applications. 相似文献
67.
Boeyens JC Cook LM Ding Y Fernandes MA Reid DH 《Organic & biomolecular chemistry》2003,1(12):2168-2172
The aryl isocyanides 1-4 are converted at 150 degrees C into the hexameric pyrazino[1,2-a:4,5-a']diindoles 15-19. 4-Fluorophenyl isocyanide, when heated at 135 degrees C, gave the hexamer 19 and the tetrameric indigo di-arylimine 9, and when kept at ambient temperature gave mainly the tetramer 9 in low yield. The structures of the hexamer 19 and the tetramer 9 were established by X-ray crystallography. Mechanisms are proposed for the oligomerisation reactions. 相似文献
68.
Using a new convergent route the synthesis of the C11 to C25 northern hemisphere fragment of the milbemycins has been achieved. 相似文献
69.
Tremayne M Grice L Pyatt JC Seaton CC Kariuki BM Tsui HH Price SL Cherryman JC 《Journal of the American Chemical Society》2004,126(22):7071-7081
A simultaneous experimental and computational search for polymorphs of chlorothalonil (2,4,5,6-tetrachloro-1,3-benzenedicarbonitrile) has been conducted, leading to the first characterization of forms 2 and 3. The crystal structure prediction study, using a specifically developed anisotropic atom-atom potential for chlorothalonil, gave as the global minimum in the lattice energy a structure that was readily refined against powder diffraction data to the known form 1 (P2(1)/a). The structure of form 2 was solved and refined from powder diffraction data, giving a disordered structure in the Rm (166) space group (Z = 3). It could also be refined against a P1 ordered model, starting from a low-energy hypothetical sheet structure found in the computational search. This shows that the disorder could be associated with the stacking of ordered sheets. The disordered structure for form 2 was later confirmed by single-crystal X-ray diffraction. The structure of form 3, determined from single-crystal diffraction, contains three independent molecules in the asymmetric unit in P2(1) (4) (Z = 6). Powder diffraction showed that this single-herringbone structure was similar to two low-energy structures found in the search. Further analysis confirmed that form 3 has a similar lattice energy and contains elements from both these predicted structures, which can be considered as good approximations to the form 3 structure. 相似文献
70.
We report complete measurement of the spectral properties of photon pairs generated via spontaneous parametric downconversion. The measurements, which include not only single-photon spectra but also two-photon joint spectra, were performed for both cw and ultrafast-pumping configurations. In agreement with theoretical predictions, the spectra for the ultrafast-pumped case reveal asymmetries that are not present with cw pumping. 相似文献