全文获取类型
收费全文 | 2390篇 |
免费 | 128篇 |
国内免费 | 5篇 |
专业分类
化学 | 2043篇 |
晶体学 | 21篇 |
力学 | 24篇 |
数学 | 68篇 |
物理学 | 367篇 |
出版年
2023年 | 18篇 |
2022年 | 20篇 |
2021年 | 32篇 |
2020年 | 58篇 |
2019年 | 43篇 |
2018年 | 31篇 |
2017年 | 24篇 |
2016年 | 56篇 |
2015年 | 76篇 |
2014年 | 88篇 |
2013年 | 119篇 |
2012年 | 178篇 |
2011年 | 179篇 |
2010年 | 97篇 |
2009年 | 99篇 |
2008年 | 191篇 |
2007年 | 173篇 |
2006年 | 169篇 |
2005年 | 157篇 |
2004年 | 120篇 |
2003年 | 74篇 |
2002年 | 67篇 |
2001年 | 42篇 |
2000年 | 32篇 |
1999年 | 20篇 |
1998年 | 17篇 |
1997年 | 20篇 |
1996年 | 16篇 |
1995年 | 12篇 |
1994年 | 12篇 |
1992年 | 16篇 |
1991年 | 11篇 |
1990年 | 8篇 |
1988年 | 8篇 |
1986年 | 8篇 |
1985年 | 21篇 |
1984年 | 8篇 |
1982年 | 11篇 |
1981年 | 11篇 |
1980年 | 11篇 |
1979年 | 8篇 |
1978年 | 15篇 |
1977年 | 10篇 |
1976年 | 16篇 |
1975年 | 11篇 |
1974年 | 16篇 |
1973年 | 17篇 |
1971年 | 11篇 |
1969年 | 8篇 |
1967年 | 8篇 |
排序方式: 共有2523条查询结果,搜索用时 15 毫秒
11.
Fumie Takei Daisuke Kodama Sugiko Nakamura Kiyotaka Onitsuka Shigetoshi Takahashi 《Journal of polymer science. Part A, Polymer chemistry》2006,44(1):585-595
Aryl isocyanides bearing free‐base and metallo‐porphyrins were prepared and polymerized with a Pd–Pt μ‐ethynediyl complex as the initiator to give polymers with narrow polydispersity indices. The molecular weights of the resulting polymers were precisely controlled by the initial feed ratio of the porphyrin monomer to the initiator. The UV–VIS spectra suggested that the porphyrin pendants are regularly arranged to form stacked columns. Metallo‐porphyrin polymers were also prepared by reacting free‐base porphyrin polymers with metal salts. The successive reactions of free‐base and zinc‐porphyrin monomers resulted in the formation of diblock polymers. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 585–595, 2006 相似文献
12.
Akikazu Matsumoto Daisuke Furukawa Hideyuki Nakazawa 《Journal of polymer science. Part A, Polymer chemistry》2006,44(17):4952-4965
We report the stereocontrol of diene polymers by the topochemical polymerization of alkoxy-substituted benzyl muconates in the solid state. A monomer stacking structure is controlled by the weak intermolecular interactions in the monomer crystals, depending on the structure and position of the alkoxy-substituent. The translational and alternating types of molecular stacking structures in a column provide diisotactic and disyndiotactic polymers, respectively, by the solid-state polymerization under UV and γ-ray irradiation. On the other hand, the meso and racemo structures of the resulting polymers are determined by the molecular symmetry of the used muconate monomers. The various substituted benzyl ester polymers are transformed into the same ethyl ester polymers with the four types of tacticities. The structure and crystallization behavior of the substituted benzyl ester polymers as well as the ethyl ester polymers have been revealed in detail. We clarify the effects of the tacticity on the crystallization property of the stereoregular polymuconates. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4952–4965, 2006 相似文献
13.
Hiroshi Aoki Ken Hosoya Tomohisa Norisuye Nobuo Tanaka Daisuke Tokuda Norio Ishizuka Kazuki Nakanishi 《Journal of polymer science. Part A, Polymer chemistry》2006,44(2):949-958
An investigation was made of the gelation of dimethacrylate‐type crosslinking agents in view of an application for separation media. The study mainly centered on a crosslinking agent, glycerol dimethacrylate (GDMA), which is relatively hydrophilic because of a hydroxyl group in the middle of its structure. The gelation of GDMA was compared with that of other hydrophobic crosslinking agents such as ethylene glycol dimethacrylate and 1,6‐hexanediol dimethacrylate. The diluents used in the study were toluene, toluene with methanol, and cyclohexanol. The gelation was observed in real time with a charge coupled device camera and dynamic light scattering (DLS). Also, the separated dry gels were extensively characterized with scanning electron microscopy, BET (N2 absorption and desorption isotherm), and Fourier transform infrared. DLS analysis showed a stronger molecular interaction of GDMA gelation in toluene, whereas this interaction was much weaker in an alcoholic solvent such as toluene with methanol or cyclohexanol. This indicated that GDMA gelation might proceed through hydrogen bonding as well as a crosslinking reaction of vinyl groups. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 949–958, 2006 相似文献
14.
15.
Tasuku Nakajima Takayuki Kurokawa Hidemitsu Furukawa Qiu Ming Yu Yoshimi Tanaka Yoshihito Osada Jian Ping Gong 《高分子科学》1996,(1):1-9
Living tissues work with fantastic functions in soft and wet gel-like state. Thus, hydrogels have attracted much attention as excellent soft & wet materials, suitable for making artificial organs for medical treatments.However, conventional hydrogels are mechanically too weak for practical uses. We have created double network (DN) hydrogels with extremely high mechanical strength in order to overcome this problem. DN gels are interpenetrating network (IPN) hydrogels consisting of rigid polyelectrolyte and soft neutral polymer. Their excellent mechanical properties cannot be explained by the standard fracture theories. In this paper, we discuss about the toughening mechanism of DN gels in accordance with their characteristic behavior, such as large hysteresis and necking phenomenon. We also describe the results on tissue engineering application of DN gels. 相似文献
16.
I. Kunugiyama N. Ito T. Ishida S. Suzuki Y. Katoh Y. Furukawa 《Journal of Radioanalytical and Nuclear Chemistry》1992,165(5):309-317
Bromine and chlorine concentrations in some tissues (liver, spleen, thymus) of healthy mice (normal group) and lymphomatous mice (lymphoma group) were determined by neutron activation analysis. There were significant differences in the Br concentrations of the tissues between the normal and lymphomatous group, while the Cl concentrations were found relatively constant in all the tissues. As a result, the Br/Cl ratios in the tissues of the lymphomatous group were significantly higher than those of the normal group. It was difficult to conclude that Br was absorbed into the bodies of lymphomatous mice more easily than was Cl. It is suggested that Br excretion from the body is suppressed. 相似文献
17.
18.
Junji Furukawa Eiichi Kobayashi Morio Nakamura 《Journal of polymer science. Part A, Polymer chemistry》1974,12(12):2789-2799
The effect of ultraviolet irradiation on the terpolymerization was investigated. In the terpolymerizations of sulfur dioxide–butene-1–acrylonitrile, sulfur dioxide–butene-1–n-butyl acrylate, and maleic anhydride–allyl chloride–acrylonitrile systems, the composition of the terpolymers prepared under ultraviolet irradiation was different from those prepared in the dark. The unit content of sulfur dioxide and butene-1 or of maleic anhydride and allyl chloride in the terpolymer increased under ultraviolet irradiation. The nature of the growing end under ultraviolet irradiation is supposed to be the same as that of the dark polymerization on the basis of the same solvent effect on the terpolymer composition, the rate of polymerization and the molecular weight of polymer. The experimental results suggest that the complex between sulfur dioxide and butene-1 or maleic anhydride and allyl chloride might be excited by ultraviolet light and the excited complex may participate in the terpolymerization. 相似文献
19.
Tomonari Wakabayashi Daisuke Kasuya Haruo Shiromaru Shinzo Suzuki Koichi Kikuchi Yohji Achiba 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1997,40(1):414-417
Systematic fractional change in the yield of various isomers of fullerenes was revealed to strongly depend on temperature of a buffer gas. A new kinetic consideration is proposed for understanding the observed temperature- and pressure-dependence of yield of fullerenes. The model consists of three competitive reactions in consideration of plausible behaviors of a precursor, (1) decomposition into smaller fragments, (2) isomerization leading to formation of a stable fullerene cage, and (3) growth into a larger carbon cluster. Arrhenius activation energy of formation of stable fullerenes was determined to be 0.8 eV for both C60 and C70, while a higher energy of 2.0?3.3 eV for seven different isomers of higher fullerenes ranging from C76 to C84. Correlation in the activation energy is noted for a series of higher fullerenes with different sizes, suggesting the existence of a specific precursor in their formation processes. 相似文献
20.
Functional poly(ethylene oxide) star polymers possessing a tertiary amino group at each arm end were prepared by free-radical copolymerization of poly(ethylene oxide) macromonomers with divinylbenzene (DVB) in water or ethanol. The poly(ethylene oxide) arm was prepared by anionic polymerization using 2-[2-(N,N-dimethylamino)ethoxy]ethanol potassium alkoxide as the initiator. The star polymers had narrow molecular weight distribution. The arm number was controlled by varying the feed ratio [DVB]/[M], the initial concentration of macromonomer [M], and solvent media. The branching factor g' in methanol ([eta]S/[eta]L are the intrinsic viscosities of the star and linear molecules, respectively) exhibited a power-law dependence on the arm number, f, with a negative exponent. This means that the dimensions of a star were in agreement with the Daoud-Cotton scaling model. 相似文献