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1.
分析了一个新的复杂的四维混沌系统的基本特性,该系统每个方程中包含一个三次交叉乘积项,共有9个平衡点,它们相对于原点和坐标轴具有完美的对称性,并且相对于线性特性和不变流形具有很好的相似性.描述了两个同时共存的对称双翼吸引子.最后,设计了一个模拟电路来实现这个新的四维混沌系统,表明数值仿真和电路实现具有很好的一致性,同时说明在应用上由于频率不同导致的仿真与物理实现之间的重要区别.
关键词:
四维混沌系统
Lyapunov 指数
共存双翼吸引子
电路实现 相似文献
2.
这篇论文综述了美国加州大学戴维斯分校科学院院士Navrotsky课题组多年来在多孔材料上取得的一系列热化学研究结果。讨论了热化学对微孔、介孔材料的结构稳定性和合成过程的影响。借助多种测热手段对影响骨架结构的热焓、热熵和自由能进行了系统的测量和计算。研究数据表明一系列纯硅分子筛、介孔材料和磷酸铝多孔材料同相应的石英相和块磷铝矿相相比能量上最多只高出15 kJ·mol-1。一系列纯硅分子筛的熵值比石英相高出3.2—4.2 J·K-1·mol-1;在0—12.6 J·K-1·mol-1范围内相对应的自由能几乎没有差别。因此,对不同微孔、介孔材料,其骨架结构在能量上是几乎没有区别的。另外,本文通过介绍一种新型测热方法——原位测热,揭示了分子筛合成过程中的动力学和成核/结晶机理。 相似文献
3.
At room temperature, three of the six polymorphic compounds described are not present in their highest melting-point form, owing to enantiotropy. These three are triphenyltin chloride (3 modifications), 1-(4,4-dimethyl-2-oxo-3-tetrahydrofuryl)thiourea (4 modifications), and 2-aminoethyl diphenylborinate (3 modifications). In the case of 4-amino-1-(2-phenylethyl)-1,2,4-triazoline-5-thione, in addition to the absolutely stable modificationI, a further six unstable crystal forms have been observed. The three modifications of,-dimethyl-[1,1-biphenyl]-4-methanol are also monotropic in character. 2,9-Dimethyl-1,10-phenanthroline, the three polymorphic forms of which are unstable, is a special case, since it absorbs water from the air and changes into a semi-hydrate. 相似文献
4.
The transition and the change in pore morphology of a porous alumina membrane prepared by anodically oxidizing aluminum in
sulfuric acid were studied mainly by TG-DTA, TMA, dilatometry and TEM. At ca. 1243 K, TMA showed an expansion followed by
contraction; the CO2 and SO2 gases were quickly discharged, and the pore morphology of the as-prepared porous membrane (ca 150 mm-t, with pores ca 25
nm in diameter and containing ca 11% by mass of SO2) showed an abrupt change, but the pores were retained to ca. 1573 K. Sulfur incorporated in the membrane was lost in two
stages, i.e., at ca 1243 K and in a range up to 1373 K. Isothermal measurements revealed the complex crystallization of the
amorphous phase into polycrystalline phase.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
5.
S. Nezu S. Walsh V. Meille M. Yoshida J. B. Lando 《Journal of polymer science. Part A, Polymer chemistry》1995,33(6):973-977
The dimer, trimer, and tetramer of 1,11-dodecadiyne, HC?C? (CH2)8? C?CH, were synthesized. The solid-state polymerization of the dimer was investigated by infrared (IR) spectroscopy. IR bands due to the diacetylene moiety were identified through the comparison of the IR spectra of the dimer, trimer, and tetramer. The dimer was found to have two polymorphs, melt-crystallized and solution-crystallized. Both of the polymorphs undergo solid-state polymerization by exposure to γ-ray or UV irradiation. The former has higher polymerizability for the diacetylene moiety than the latter. The solid-state polymerization of the terminal acetylene group was not observed. It is shown that the previously reported dimer structure in which both the diacetylene and terminal acetylene groups are polymerized to form an inherently electrically conducting polymer is incorrect. © 1995 John Wiley & Sons, Inc. 相似文献
6.
J.G. Zhao 《Journal of solid state chemistry》2007,180(10):2816-2823
The single-phase 6H BaRuO3 with the hexagonal BaTiO3 structure was synthesized at 5 GPa and 1000 °C. Rietveld refinement of the powder X-ray data for the 6H phase resulted in the lattice parameters to be a=5.7127(1) Å and c=14.0499(2) Å; the average Ru-O distance and direct Ru-Ru distance in the Ru2O9 dioctahedron being 1.992(6) and 2.5658(14) Å, respectively. The electrical resistivity of the 6H BaRuO3 follows a relationship of ρ versus T3/2 below 60.0 K, a signature deviation from the Fermi-liquid behavior. Both magnetic susceptibility and specific heat data indicate that the 6H BaRuO3 is an exchange-enhanced Pauli paramagnet due to the electron correlation effect with large Wilson ratio RW and Stoner enhancement factor. The comprehensive evolution of transport and magnetic properties from 9R across 4H to 6H BaRuO3 was discussed. 相似文献
7.
构造一个具有复合幂函数的三维连续自治混沌系统。系统的状态方程仅有5项,其中一项是指数小于1的复合幂函数。该系统具有结构简单、非双曲平衡点、吸引子共存的性质,展现出了复杂的动力学行为。首先,对系统的动力学行为进行分析,包括李雅普诺夫(Lyapunov)指数谱、分岔图以及庞加莱映射等,结果表明此系统具有混沌特性。然后进行混沌系统的电路设计,电路仿真结果验证了理论分析的正确性。 相似文献
8.
9.
Formation, crystal structure, polymorphism, and transition between polymorphs are reported for M(thd)3, (M = Al, Cr, Mn, Fe, Co, Ga, and In) [(thd)– = anion of H(thd) = C11H20O2 = 2, 2, 6, 6‐tetramethylheptane‐3, 5‐dione]. Fresh crystal‐structure data are provided for monoclinic polymorphs of Al(thd)3, Ga(thd)3, and In(thd)3. Apart from adjustment of the M–Ok bond length, the structural characteristics of M(thd)3 complexes remain essentially unaffected by change of M. Analysis of the M–Ok, Ok–Ck, and Ck–Ck distances support the notion that the M–Ok–Ck–Ck–Ck–Ok– ring forms a heterocyclic unit with σ and π contributions to the bonds. Tentative assessments according to the bond‐valence or bond‐order scheme suggest that the strengths of the σ bonds are approximately equal for the M–Ok, Ok–Ck, and Ck–Ck bonds, whereas the π component of the M–Ok bonds is small compared with those for the Ok–Ck, and Ck–Ck bonds. The contours of a pattern for the occurrence of M(thd)3 polymorphs suggest that polymorphs with structures of orthorhombic or higher symmetry are favored on crystallization from the vapor phase (viz. sublimation). Monoclinic polymorphs prefer crystallization from solution at temperatures closer to ambient. Each of the M(thd)3 complexes subject to this study exhibits three or more polymorphs (further variants are likely to emerge consequent on systematic exploration of the crystallization conditions). High‐temperature powder X‐ray diffraction shows that the monoclinic polymorphs convert irreversibly to the corresponding rotational disordered orthorhombic variant above some 100–150 °C (depending on M). The orthorhombic variant is in turn transformed into polymorphs of tetragonal and cubic symmetry before entering the molten state. These findings are discussed in light of the current conceptions of rotational disorder in molecular crystals. 相似文献
10.
Dr. Andrea Previtali Dr. Wei He Dr. Alessandra Forni Dr. Daniele Malpicci Dr. Elena Lucenti Dr. Daniele Marinotto Prof. Lucia Carlucci Prof. Pierluigi Mercandelli Dr. Marco Aldo Ortenzi Prof. Giancarlo Terraneo Dr. Chiara Botta Prof. Ryan Tsz Kin Kwok Dr. Jacky Wing Yip Lam Prof. Ben Zhong Tang Prof. Elena Cariati 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(67):16690-16700
Organic materials with multiple emissions tunable by external stimuli represent a great challenge. TTPyr, crystallizing in different polymorphs, shows a very rich photophyisics comprising excitation-dependent fluorescence and phosphorescence at ambient conditions, and mechanochromic and thermochromic behavior. Transformation among the different species has been followed by thermal and X-ray diffraction analyses and the emissive features interpreted through structural results and DFT/TDDFT calculations. Particularly intriguing is the polymorph TTPyr(HT), serendipitously obtained at high temperature but stable also at room temperature, whose non-centrosymmetric structure guarantees an SHG efficiency 10 times higher than that of standard urea. Its crystal packing, where only the TT units are strongly rigidified by π-π stacking interactions while the Pyr moieties possess partial conformational freedom, is responsible for the observed dual fluorescence. The potentialities of TTPyr for bioimaging have been successfully established. 相似文献