全文获取类型
收费全文 | 539篇 |
免费 | 30篇 |
国内免费 | 1篇 |
专业分类
化学 | 413篇 |
晶体学 | 12篇 |
力学 | 8篇 |
数学 | 40篇 |
物理学 | 97篇 |
出版年
2022年 | 3篇 |
2021年 | 3篇 |
2020年 | 5篇 |
2018年 | 12篇 |
2017年 | 6篇 |
2016年 | 8篇 |
2015年 | 14篇 |
2014年 | 11篇 |
2013年 | 34篇 |
2012年 | 19篇 |
2011年 | 30篇 |
2010年 | 19篇 |
2009年 | 15篇 |
2008年 | 50篇 |
2007年 | 29篇 |
2006年 | 33篇 |
2005年 | 27篇 |
2004年 | 24篇 |
2003年 | 20篇 |
2002年 | 20篇 |
2001年 | 7篇 |
2000年 | 3篇 |
1999年 | 3篇 |
1998年 | 5篇 |
1997年 | 3篇 |
1996年 | 7篇 |
1995年 | 5篇 |
1994年 | 3篇 |
1993年 | 6篇 |
1992年 | 7篇 |
1991年 | 2篇 |
1990年 | 4篇 |
1989年 | 2篇 |
1988年 | 5篇 |
1987年 | 2篇 |
1986年 | 7篇 |
1985年 | 7篇 |
1984年 | 8篇 |
1983年 | 7篇 |
1982年 | 11篇 |
1981年 | 12篇 |
1980年 | 12篇 |
1979年 | 7篇 |
1978年 | 9篇 |
1977年 | 12篇 |
1976年 | 7篇 |
1975年 | 6篇 |
1974年 | 5篇 |
1973年 | 2篇 |
1962年 | 2篇 |
排序方式: 共有570条查询结果,搜索用时 15 毫秒
31.
Shotaro Hayashi Fumitaka Ishiwari Takanori Fukushima Shohei Mikage Yutaka Imamura Motomichi Tashiro Michio Katouda 《Angewandte Chemie (International ed. in English)》2020,59(37):16195-16201
Elastic organic crystals have attracted considerable attention as next‐generation flexible smart materials. However, the detailed information on both molecular packing change and macroscopic mechanical crystal deformations upon applied stress is still insufficient. Herein, we report that fluorescent single crystals of 9,10‐dibromoanthracene are elastically bendable and stretchable, which allows a detailed investigation of the deformation behavior. We clearly observed a Poisson effect for the crystal, where the short axes (b and c‐axes) of the crystal are contracted upon elongation along the long axis (a‐axis). Moreover, we found that the Poisson's ratios along the b‐axis and c‐axis are largely different. Theoretical molecular simulation suggests that the tilting motion of the anthracene may be responsible for the large deformation along the c‐axis. Spatially resolved photoluminescence (PL) measurement of the bent elastic crystals reveals that the PL spectra at the outer (elongated), central (neutral), and inner (contracted) sides are different from each other. 相似文献
32.
Michio Kurosu Katsuhiko Mitachi Junshu Yang Edward V. Pershing Bruce D. Horowitz Eric A. Wachter John W. Lacey III Yinduo Ji Dominic J. Rodrigues 《Molecules (Basel, Switzerland)》2022,27(1)
Rose bengal has been used in the diagnosis of ophthalmic disorders and liver function, and has been studied for the treatment of solid tumor cancers. To date, the antibacterial activity of rose bengal has been sporadically reported; however, these data have been generated with a commercial grade of rose bengal, which contains major uncontrolled impurities generated by the manufacturing process (80–95% dye content). A high-purity form of rose bengal formulation (HP-RBf, >99.5% dye content) kills a battery of Gram-positive bacteria, including drug-resistant strains at low concentrations (0.01–3.13 μg/mL) under fluorescent, LED, and natural light in a few minutes. Significantly, HP-RBf effectively eradicates Gram-positive bacterial biofilms. The frequency that Gram-positive bacteria spontaneously developed resistance to HP-RB is extremely low (less than 1 × 10−13). Toxicity data obtained through our research programs indicate that HP-RB is feasible as an anti-infective drug for the treatment of skin and soft tissue infections (SSTIs) involving multidrug-resistant (MDR) microbial invasion of the skin, and for eradicating biofilms. This article summarizes the antibacterial activity of pharmaceutical-grade rose bengal, HP-RB, against Gram-positive bacteria, its cytotoxicity against skin cells under illumination conditions, and mechanistic insights into rose bengal’s bactericidal activity under dark conditions. 相似文献
33.
Michio Iwaoka Shuji Tomoda 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3-4):755-766
Weak nonbonded interaction between a divalent selenium and an oxygen atom (i.e., Se···O interaction) frequently plays important roles in chemical and biological functions of selenium compounds. To establish that 77 Se NMR is an easy experimental probe to diagnose the strength of an Se···O interaction, 3 series of 2-substituted benzeneselenenyl derivatives, which have an intramolecular Se···O interaction in solution, were employed. By comparing the 77 Se NMR chemical shifts (δ Se ) with those observed for other series of selenium compounds, which have an intramolecular Se···Y (Y = N, O, F, Cl, or Br) interaction, approximate linear correlation was found between the δ Se values and the strengths of the nonbonded Se···Y interactions evaluated by natural bond orbital analysis at the B3LYP level. The correlation will be useful for estimating the strength of an Se···O interaction simply from the 77 Se NMR chemical shift. By extending the chemistry of nonbonded Se···O interactions to structural biology, analogous S···O interactions have been discovered in protein architecture. The directional features were, however, different from those of Se···O and S···O interactions of small organic compounds. 相似文献
34.
[structure: see text] Covalently linked dimers of amphotericin B were prepared by cross-linking its carboxylic acid. Among these, a dimer with a linkage of 1,6-hexanediamine revealed potent hemolytic activity (EC50, 0.25 microM) while its N-acetyl derivative gave rise to large K+ ion flux in phosphatidylcholine liposomes, regardless of the presence or absence of sterols, suggesting that the dimers may serve as a tool for elucidating the structure of the ion channel assemblage formed by amphotericin B. 相似文献
35.
Michio Kimura Stanley H. Simonsen Steven R. Caldwell Gary E. Martin 《Journal of heterocyclic chemistry》1981,18(3):469-473
The single crystal X-ray diffraction structure of 2-(2′-pyridylthio)-3-nitropyridine is reported. A non-bonded interaction was observed between the sulfur atom and one of the oxygen atoms of the nitro group with an interatomic distance of 2.678 A. Examination of the molecule's behavior in solution by 13C-nmr spin-lattice (T1) relaxation measurements showed the non-nitro bearing pyridyl ring to reorient anisotropically about the C2′-C5′ bond axis. In contrast, the nitro substituted pyridine ring did not appear to exhibit anisotropic reorientation about the corresponding C2-C5 bond axis. Rather, approximately equivalent relaxation times were noted for all protonated ring carbons, indicating that the relaxations of this portion of the molecule were governed by the overall isotropic reorientation of the system. Based on these observations, it was concluded that the intramolecular sulfur-nitro interaction also operates in the solution state and is sufficiently strong to prevent free rotation of the substituted portion of the molecule about the C2-S bond axis. 相似文献
36.
Hisashi Odani Masaki Uchikura Yukimasa Ogino Michio Kurata 《Journal of membrane science》1983,14(2):193-208
Diffusion and solution behavior of methanol vapor in two diblock copolymers, poly(2-vinylpyridine)—block—polyisoprene [P(2VPbI)] and poly(2-vinylpyridine)—block—polystyrene [P(2VPbS)], was studied by the weighing method at 25°C. The domain structure of films of both copolymers showed an alternating lamellar arrangement. Methanol is a good solvent for P2VP, but a nonsolvent for PI and PS. Methanol dissolved exclusively in the P2VP phase of the copolymers. For both copolymer systems, absorption and desorption processes of non-Fickian type were observed as characterized by a thickness anomaly. However, the magnitude of the deviations from purely Fickian behavior was small, and the integral diffusion coefficient, D?, was obtainable with reasonable accuracy. At low and medium concentrations, D? for P(2VPbI) was greater, by about one order of magnitude, than that for P2VP, while D? for P(2VPbS) was lower than that for P2VP. A similar trend was observed in plots of the permeability coefficient against the vapor pressure of methanol. The results indicate that the rubbery PI phase may facilitate the transport of penetrant molecules in the P(2VPbI) film. On the other hand, the glassy PS phase in the P(2VPbS) film merely interferes with the transport of methanol molecules. 相似文献
37.
Masanori Yoshikawa Michio Sorai Hiroshi Suga Syŭzŏ Seki 《Journal of Physics and Chemistry of Solids》1983,44(4):311-321
Heat capacity measurements have been made for six kinds of specimens prepared by different methods. Among them, Sample A exhibited a A-type ferromagnetic pahse transition at 1.347 K and a Schottky-type anomaly due to the zero-field splitting around 9K. The total entropy and enthalpy were (11.05 ± 0.04) J K?1mol?1 and (97.0 ± 0.4) J mol?1, respectively. Sample B exhibited a Sehottky-type anomaly around 0.4 K due to the ferro-magnetic dimeric coupling with as well as the Schottky-type anomaly at 9K. The total magnetic entropy and enthalpy were (11.45 ± 0.03) JK?1 mol?1 and (93.8 ± 0.8) J mol?1, respectively. The remaining samples are simple mixtures of the λ-type modification and the dimeric modification. Irrespective of the magnetic behavior at low temperatures, all the samples showed a non-magnetic first-order phase transition around 270 K. The heat capacity and entropy of this phase transition have been accounted for in terms of the Frenkel theory of heterophase fluctuation. Construction of an adiabatic-type calorimeter workable between 1.5 and 393 K has been also presented. 相似文献
38.
39.
The 3.51 μm HeXe laser is magnetically tuned over a wavenumber of 0.2 cm?1 and used for infrared absorption and double resonance spectroscopy. Eight rotation-vibration lines of propynal in the ν2 band are assigned by the Stark effect. Eleven microwave transitions in the v2 = 1 vibrational state are observed by the method of infrared-microwave double resonance. The rotational constants of the excited state and the band origin of the vibration ν2 are determined from the observed spectra. 相似文献
40.