全文获取类型
收费全文 | 73篇 |
免费 | 1篇 |
专业分类
化学 | 64篇 |
力学 | 2篇 |
数学 | 2篇 |
物理学 | 6篇 |
出版年
2014年 | 1篇 |
2013年 | 6篇 |
2011年 | 1篇 |
2010年 | 2篇 |
2008年 | 1篇 |
2007年 | 2篇 |
2006年 | 1篇 |
2003年 | 1篇 |
2002年 | 3篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1997年 | 1篇 |
1996年 | 1篇 |
1995年 | 1篇 |
1992年 | 2篇 |
1991年 | 1篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 4篇 |
1986年 | 1篇 |
1985年 | 3篇 |
1984年 | 7篇 |
1982年 | 5篇 |
1981年 | 6篇 |
1980年 | 5篇 |
1979年 | 4篇 |
1976年 | 2篇 |
1974年 | 2篇 |
1973年 | 2篇 |
1972年 | 2篇 |
1969年 | 1篇 |
排序方式: 共有74条查询结果,搜索用时 31 毫秒
1.
This paper presents a simplified optical method for measuring the residual stresses by rapid cooling in thermosetting resin
strips. First, the fundamental equations for calculating the residual stress from the residual birefringence were obtained
by the linear photoviscoelastic theory. The specimens were then subjected to rapid cooling. After rapid cooling, the residual
stress was measured by two methods, the simplified optical method mentioned above and the well-known layer-removal method.
The effectiveness of the simplified optical method was discussed by comparing results of the two methods. 相似文献
2.
It is demonstrated that the first-order relativistic correction term to the Schrödinger hamiltonian for the hydrogen-like atom, cannot be used safely even for small values of atomic number, Z, in the variational calculation. A modified form of the operator R is proposed so that one may incorporate it into the variational treatment of molecular systems. 相似文献
3.
Minimal contracted Gaussian basis sets are presented for Ga through Cd. Characteristically these Gaussian-based minimal sets give far better d orbital energies than those by minimal STO basis sets. These new basis sets were tested on Br2 for which a new benchmark calculation was also performed. The test result is satisfactory in that these basis sets produce good general agreement with the near Hartree–Fock calculation with respect to the molecular spectroscopic constants. 相似文献
4.
Treatment of 3-acetonyl-5-cyano-1,2,4-thiadiazole (1) with 4-methyl or 4-methoxyphenylhydrazine hydrochloride provided 5-cyano-3-(2,5-dimethylindol-3-yl)-1,2,4-thiadiazole (2) or 5-cyano-3-(5-methoxy-2-methylindol-3-yl)-1,2,4-thiadiazole (3) as the sole product, respectively. In contrast, treatment of 1 with phenylhydrazine hydrochloride resulted in the formation of 5-cyano-3-(2-methylindol-3-yl)-1,2,4-thiadiazole (4) and the unexpected 5-cyano-3-(3,5-dimethyl-1-phenylpyrazol-4-yl)-1,2,4-thiadiazole (5). In a similar manner, when 1 was treated with 4-chlorophenylhydrazine hydrochloride, indolization was suppressed by phenylpyrazolation giving rise to 5-cyano-3-(5-chloro-2-methylindol-3-yl)-1,2,4-thiadiazole (6) and 5-cyano-3-[1-(4-chlorophenyl)-3,5-dimethylpyrazol-4-yl]-1,2,4-thia diazole (7). The reaction mechanism is discussed. Compounds 4, 5 and 6 exhibited weak antimicrobial activity against Helicobacter pylori. 相似文献
5.
A novel α-phenylselenenylation of carbonyl compounds has been performed by electrolysis of a solution of ketones, diphenyl diselenide, tetraethylammonium bromide, and magnesium bromide in polar solvents (MeOH, AcOH, MeCN). The electrolysis enables us to prepare the desired seleno-carbonyl compounds without employing strong bases and the activated selenenyl reagents PhSeX. 相似文献
6.
d1-Theaspirane (1) was prepared by the selenium-mediated electrochemical oxidation of α-dihydroionol (3), via a novel selenium-mediated spiroannelation. 相似文献
7.
Fukuji Higashi Shigeru Sugimori Toshio Mashimo 《Journal of polymer science. Part A, Polymer chemistry》1988,26(4):1003-1009
The direct polyesterification with thionyl chloride (SOCl2) in pyridine was further investigated. Copolycondensations of dicarboxylic acids, bisphenols, and hydroxybenzoic acids were significantly affected by the reaction temperatures and combinations of monomers which could change relative rates of alcoholyses of the activated dicarboxylic acids and the hydroxyacids consequently to vary monomer sequences in the copolymers resulted. The sequences were tried to be varied more directly by stepwise reactions of monomers in copolycondensations of dicarboxylic acids, bisphenols, and p-hydroxybenzoic acid (PHB), as well as PHB and m-hydroxybenzoic acid (MHB). The reactions proceeded smoothly and satisfactorily when carried out by initial reaction of dicarboxylic acids and PHB followed by bisphenols likely to favor sequential to random distributions of monomers. Reverse addition of PHB and bisphenols, and then dicarboxylic acids resulted in rapid precipitation due to some oligomerization of PHB at an earlier stage of reaction, and largely retarded the reaction. This was also the case for the copolycondensation of PHB and MHB. Copolymers of high inherent viscosities with up to 65 mol% PHB could be obtained by initial reaction of MHB followed by PHB. 相似文献
8.
New ring-opening reaction of thiazoline-azetidinones 1 to dithioazetidinones 2 was achieved with 2-benzothiazolyl disulfide in aqueous acidic media and its potentiality for the preparation of a variety of cephalosporins 3 from various thiazoline-azetidinones 1 is demonstrated. 相似文献
9.
57Fe Mössbauer spectra were measured of reaction products formed during an incubation experiment with sulfate-reducing bacteria, which were isolated from estuarine sediments of the Tama River in Tokyo. The spectrum of the product incubated for several days showed some overlapping sextets. This product had a different chemical form from amorphous iron monosulfide produced by inorganic reaction between ferrous and sulfide ions. It was estimated that the structure of nearest neighbor of iron in this product was similar to that of pyrrhotite (Fe1?x S). After several months of incubation, other singlet and doublet appeared successively on the spectrum, corresponding to mackinawite (FeS1?x ) and new sulfide, respectively. Both values of isomer shift and quadrupole splitting of new sulfide increased with increasing incubation time and approached those of pyrite (FeS2). Extended X-ray absorption fine structure (EXAFS) showed that iron atoms were coordinated by sulfur in the incubation product. 相似文献
10.
Takeshi Miyakawa Ryota Morikawa Masako Takasu Kimikazu Sugimori Kazutomo Kawaguchi Hiroaki Saito 《Molecular physics》2014,112(3-4):526-532
We investigate the structures of the Hras-GTP and the Hras-GDP complexes in water solvents in order to understand the mechanism of GTP hydrolysis in the Hras-GTP complex. We performed MD simulations of these complexes in order to study the positions and the orientations of water molecules around the guanosine nucleotides. Using trajectories we calculated the angular distribution of water molecules around the most distant phosphorus from guanosine in our previous work. It was shown that water molecules are distributed evenly in GTP, although unevenly in GDP. This suggests that the trigger of GTP hydrolysis is possibly the attack of water molecule to γ?phosphate from the appropriate direction. In this paper, in order to investigate the role of water molecules in GTP hydrolysis in detail, we calculate the orientation of water molecules. The distribution of the orientation is different between GTP and GDP. In order to investigate the cause of this difference, we examine the hydrogen bonds between water molecules and oxygen atom of the most distant phosphate from guanosine. We find that these hydrogen bonds are formed. We also find that the oxygen atom of hydrogen bond is determined by the position of the water molecule of hydrogen bond. 相似文献