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排序方式: 共有135条查询结果,搜索用时 15 毫秒
1.
K. Niume K. Toyofuku F. Toda K. Uno M. Hasegawa Y. Iwakura 《Journal of polymer science. Part A, Polymer chemistry》1982,20(3):663-673
Polybenzimidazoles that contained anthracene photodimer were prepared. The molecular weights of the polymers prepared by the photopolymerization of bis-anthrylbenzimidazoles were limited by the precipitation of the resulting polymers from the reaction organic solvents. Higher molecular weight polymers were obtained by the photopolymerization of bis-anthryl-Schiff's bases, followed by the oxidation of the resulting polymers. These polymers were soluble in acidic solvents such as formic and sulfuric acids but were insoluble in organic solvents. 相似文献
2.
Yoshio Iwakura Kohji Noguchi 《Journal of polymer science. Part A, Polymer chemistry》1969,7(3):801-812
A series of polyguanidines was prepared by the polyaddition reaction of biscarbodiimides with diamines. The polyaddition reaction was carried out in solution. The polymers thus obtained had intrinsic viscosities up to 0.84 and molecular weights up to 15000. The structure of the polymers was identified by comparison of their infrared spectra with those of model compounds, elementary analysis, and a study of the reaction conditions. Thermogravimetric study indicated that the polyguanidines decomposed over 170°C under nitrogen. The polyguanidines were highly resistant to hydrolytic degradation by strong acid or alkali. The polyguanidines had basic groups and formed stable hydrochloric salts when they were treated with hydrochloric acid. 相似文献
3.
K. Uno M. Makita S. Ooi Y. Iwakura 《Journal of polymer science. Part A, Polymer chemistry》1968,6(2):257-267
Copolymerization of methacrylic esters derived from glycidyl methacrylate and nucleophiles with styrene was carried out. The monomer reactivity ratios of these methacrylic esters were varied with the alkoxy groups of the esters and the solvent used. 相似文献
4.
Masanao Oya Keikichi Uno Yoshio Iwakura 《Journal of polymer science. Part A, Polymer chemistry》1972,10(2):613-623
Copolymerization of NCA's was undertaken in a heterogeneous system in acetonitrile, which is not a solvent of the polypeptides. The reactivity ratio was calculated by using the Lewis-Mayo equation. Further, the conversion rate in the copolymerization and the configuration of the copolymer produced were compared with those of the copolymerization in the homogeneous system in nitrobenzene, in which the copolypeptides are swollen. The rate of copolymerization in acetonitrile was between the rates of polymerization of the individual monomers. It has been reported that the configuration of the copolymer obtained in dimethylformamide, in which the copolypeptides are swollen, is of the block type. On the other hand, many polypeptides obtained in acetonitrile, which is not a solvent of the copolypeptides, had a random configuration near to an alternating configuration. 相似文献
5.
Yoshinori Kadoma Takashi Toida Kenji Takeda Keikichi Uno Yoshio Iwakura 《Journal of polymer science. Part A, Polymer chemistry》1975,13(3):707-716
The polymerization of picryl (PMA), 2,4-dinitrophenyl (2,4-DNMA),2,6-dinitrophenyl (2,6-DNMA), 2-methyl-4,6-dinitrophenyl (MDNMA), and 2,6-dimethylphenyl methacrylates (DMMA) was carried out in benzene at 60°C. PMA, 2,6-DNMA, and MDNMA did not undergo radical homopolymerization, while 2,4-DNMA and DMMA did. The results suggest that the growing radical readily attacks the oxygen atom of the nitro group at the 2 position of the terminal phenyl group due to the steric effect of the substituent at the 6 position, resulting in chain termination. PMA formed a charge-transfer complex with 2-naphthyl methacrylate (NMA). The stoichiometric composition of this complex was shown to be 1:1 molar complex. PMA was readily copolymerized with NMA. The amount of solvent affected the composition of the copolymer obtained at a given same mole fraction in feed. The results suggest that charge-transfer interaction between the ester groups affects the copolymerization mechanism. 相似文献
6.
Yasuo Saegusa Sakayu Iida Shigeo Nakamura Nguyen Chau Yoshio Iwakura 《Journal of polymer science. Part A, Polymer chemistry》1984,22(5):1017-1023
Aromatic polythioamide-oxothioxoquinazolines were synthesized by the polycondensation of 2,2′-(m-phenylene)bis-1,3,4-thiadiazoline-5-thione with aromatic bis-o-amino esters. The polymerizations were carried out at 160°C in acidic media such as m-cresol, sulfolane, and polyphosphoric acid to produce polymers with reduced viscosities up to 0.5 dL/g. These polymers were soluble in polar aprotic solvents like N-methyl-2-pyrrolidone and some acidic media including m-cresol. The polythioamide-oxothioxoquinazolines showed relatively good thermal stability with 10% weight loss at 344–394°C in air. 相似文献
7.
Yoshio Iwakura Fujio Toda Kenjiro Hattori 《Journal of polymer science. Part A, Polymer chemistry》1968,6(6):1633-1642
New vinylsilanes (M2), i. e. phenylvinylsilane (I), allylmethylsilane (II), allylphenylsilane (III), and p-vinylphenylmethylsilane (IV), were prepared and copolymerized with styrene (M1). The monomer reactivity ratios were r1 = 5.7 and r2 = 0, r1 = 36 and r2 = 0, r1 = 29 and r2 = 01, and r1 = 0.91 and r2 = 1.1, respectively. From the results of infrared and NMR spectra it was indicated that the vinylsilanes participated in copolymerization in the form of a vinyl type of polymerization and not in the form of a hydrogen-transfer type of polymerization. The reaction of copolymer with alcohols and methyl methacrylate and appropriate catalysts was investigated. 相似文献
8.
Yoshio Iwakura Fusakazu Hayano 《Journal of polymer science. Part A, Polymer chemistry》1969,7(2):597-607
Polyimides having pendant hydroxy groups were prepared by addition of pyromellitimide with bisepoxides. Tertiary amines and quaternary ammonium halides were effective as a catalyst. The polyimides were soluble in dichloroacetic acid and had inherent viscosities in the range 0.16–0.19 dl/g. Thermogravimetric analysis showed that a rapid weight loss of the polymers occurred at about 400°C. The pendant hydroxy groups were easily acetylated by treating the polymers with a mixture of acetic anhydride and pyridine. The acetylated polyimides were soluble in dimethylformamide, dimethylacetamide, and dioxane and melted at 120–150°C. 相似文献
9.
Masao Matsuoka Tsuyoshi Matsuda June Tamaki Yoshifumi Yamamoto Chiaki Iwakura 《Research on Chemical Intermediates》2006,32(5):389-402
Laves-phase hydrogen storage alloy has a high potential for use as negative electrode material as alternative for the misch-metal-based
material. In order to improve the energy density and the rate capability of negative electrode, chemical and mechanical modification
of Lavesphase alloy with different stoichiometric ratios was carried out. Discharge capacity and high-rate dischargeabilty
was evaluated by electrochemical methods and the characterization of Laves-phase alloy was made by X-ray diffraction, SEM
observation and PCT measurement. The best result in discharge capacity could be obtained for stoichiometric Laves-phase alloy
with a composition of Zr0.9Ti0.1Ni1.1Co0.1Mn0.5V0.2Cr0.1 by boiling in 10 M KOH solution. On the other hand, the high-rate dischargeability was increased remarkably by introducing
mechanical grinding before alkali treatment. The cause for improved performance was discussed on the basis of thermodynamic
stability of metal hydride and changes in crystal structure and surface morphology influencing on diffusion coefficient and
diffusion path length of hydrogen. 相似文献
10.
Yoshio Iwakura Keikichi Uno Shigeyoshi Hara Shigeru Kurosawa 《Journal of polymer science. Part A, Polymer chemistry》1968,6(12):3381-3393
A new ring-opening reaction of 1,3,4-oxadiazole by methylating reagents was developed in fuming sulfuric acid or polyphosphoric acid and then, by applying this reaction to poly-p-phenylene-1,3,4-oxadiazole, a high molecular weight poly-N-methylterephthalylhydrazide was obtained. Various methylating reagents were investigated as ring-opening reagents. The degrees of ring-opening in polymers were estimated and related to the properties of the polymers. 相似文献