全文获取类型
收费全文 | 207篇 |
免费 | 0篇 |
国内免费 | 1篇 |
专业分类
化学 | 148篇 |
晶体学 | 2篇 |
力学 | 4篇 |
物理学 | 54篇 |
出版年
2022年 | 3篇 |
2021年 | 4篇 |
2020年 | 2篇 |
2019年 | 2篇 |
2018年 | 2篇 |
2017年 | 2篇 |
2016年 | 1篇 |
2014年 | 1篇 |
2013年 | 6篇 |
2012年 | 4篇 |
2011年 | 10篇 |
2010年 | 5篇 |
2009年 | 9篇 |
2008年 | 13篇 |
2007年 | 6篇 |
2006年 | 6篇 |
2005年 | 14篇 |
2004年 | 19篇 |
2003年 | 10篇 |
2002年 | 12篇 |
2001年 | 6篇 |
2000年 | 8篇 |
1999年 | 4篇 |
1998年 | 4篇 |
1997年 | 1篇 |
1996年 | 3篇 |
1994年 | 1篇 |
1990年 | 2篇 |
1989年 | 2篇 |
1988年 | 3篇 |
1987年 | 2篇 |
1986年 | 2篇 |
1985年 | 7篇 |
1984年 | 4篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1981年 | 4篇 |
1980年 | 1篇 |
1979年 | 4篇 |
1978年 | 3篇 |
1977年 | 3篇 |
1976年 | 2篇 |
1975年 | 3篇 |
1974年 | 3篇 |
1973年 | 3篇 |
排序方式: 共有208条查询结果,搜索用时 15 毫秒
81.
82.
83.
Determination of the oxidation states of bismuth and copper in superconductor Bi-Ca-Sr-Cu-O by oxidation-reduction titration 总被引:1,自引:0,他引:1
Masaoki Oku Jin Kimura Mamoru Omori Kichinosuke Hirokawa 《Fresenius' Journal of Analytical Chemistry》1989,335(4):382-385
Summary The oxidation state of the superconductor Bi-Ca-Sr-Cu-O was determined by two procedures. One was ferrous-chromate titration after dissolution of the sample in manganous nitrate solution. The other was the titration after dissolution in ferrous ion solution. The former procedure gives the concentration of a state like pentavalent bismuth and the latter gives the sum of concentrations of a state like pentavalent bismuth and a state like trivalent copper or peroxide. The result of the titration shows that the superconductor oxide has the state like pentavalent bismuth but not like that of trivalent copper. This is a striking contrast to YBa2Cu3O7–y having a high concentration of the latter state. Although the result was compared with X-ray photoelectron spectra, a clear relationship between them was not obtained.
Bestimmung der Oxidationsstufen von Bismut und Kupfer im Supraleiter Bi-Ca-Sr-Cu-O durch Redoxtitration相似文献
84.
Abstract— Quenching of excited state of Ru(bpy)2 (poly-4-methyl-4'-vinyl-2,2'-bipyridine)Cl2 by sodium anthraquinone-2-sulfonate was found to be a static process. The quenching was interpreted by application of a modified Perrin model. Radius of the quenching sphere was estimated to correspond to 6.65 monomer units and was unchanged on varying the Ru2 + content of the polymer. Energy migration along the polymer chain was denied. 相似文献
85.
Abstract— Changes in the UV absorption spectrum with the photoconversion of Chenopodium chlorophyll protein, CP668 ⇆ CP743, and with the pH change of the CP668 and CP743 solutions, were measured. The change in the absorption spectrum of the apoprotein caused by the pH change was reversible, whereas that caused by the photoconversion was irreversible. The apoprotein may undergo a proton dissociation or association of the phenolic group in tyrosine residues upon pH change. A photooxidation in CP668 (loss of electron) caused by irradiation of CP668 solution may induce a change in the ionization state of some amino acid residues. The isoelectric points of CP668 and CP743 were determined to be 9.3 and 7.2, respectively. 相似文献
86.
Harada T Egusa T Igarashi Y Kinugasa M Oku A 《The Journal of organic chemistry》2002,67(20):7080-7090
Acetals derived from racemic 1,3-alkanediols undergo kinetic resolution in chiral oxazaborolidinone-mediated ring-cleavage reaction with nucleophiles such as enol silanes and allylic silanes. Enantioselectivity of the reaction is affected by nucleophiles, the N-sulfonyl groups of oxazaborolidinones, and the substituents attached to the acetal carbon. For disubstituted acetals rac-1 and for trisubstituted acetal rac-2, derived from syn-2,4-dimethyl-1,3-pentanediol, satisfactory enantioselectivity is obtained by using methallylsilane 7b,c as a nucleophile in combination with N-mesyloxazaborolidinone 4a. On the other hand, enantioselective reaction of trisubstituted acetal rac-3b, derived from anti-2,4-dimethyl-1,3-pentanediol, is realized by using silyl ketene acetal 5e in combination with N-tosyloxazaborolidinone 4b. The reaction conditions optimized for the kinetic resolution, or enantiomer differentiating reaction, of the racemic acetals are successfully applied to asymmetric desymmetrization of meso-1,3-polyols through intramolecular differentiation of the enantiotopic acetal moieties of the bis-acetal derivatives. The utility of the ring-cleavage reaction as a method for enantioselective terminal differentiation of prochiral polyols is demonstrated in convergent asymmetric synthesis of pentol derivative 35 corresponding to the C(19)[bond]C(27) ansa-chain of rifamycin S. 相似文献
87.
Kaoru Iwai Yoshihiro Itoh Masaoki Furue Shun-Ichi Nozakura 《Journal of polymer science. Part A, Polymer chemistry》1983,21(8):2439-2449
The exciplex formation in 9-vinylphenanthrene-p-N,N-dimethylaminostyrene copolymers, its characteristics, and the electron transfer process in polar solvents were studied. The copolymer exhibited a more intense intramolecular exciplex fluorescence than the low-molecular-weight model system, phenanthrene-N,N-dimethylaniline, in which the intermolecular exciplex formation occurred. Intensities of the exciplex fluorescence, which were unchanged regardless of the copolymer composition, led us to speculate that the efficient energy migration takes place from an excited phenanthrene unit to an exciplex forming site on the polymer chain. The electron transfer in the copolymer-p-dicyanobenzene system was studied in polar media. The formation of p-dicyanobenzene anion radical was measured by flash photolysis and electron spin resonance (ESR). p-Dicyanobenzene anion radical was generated by the electron transfer process via exciplex and the direct electron transfer process from the excited phenanthrene unit in the copolymer. 相似文献
88.
Toshiro Harada Shin-ichiro Matsui Tran Mai Thi Tuyet Masanori Hatsuda Shinji Ueda Akira Oku Motoo Shiro 《Tetrahedron: Asymmetry》2003,14(24):3879-3884
Asymmetric synthesis of 24- and 26-membered macrocyclic binaphthol dimers was achieved by assembling a 3,3′-diethynyl-1,1′-bi-2-naphthol unit and 1,2- and 1,3-phenylene units with Sonogashira coupling reaction. 相似文献
89.
Ketone dilithio α,β- and α,β′-dianions can be generated by a tin-lithium exchange reaction of the lithium enolate of β-tributyltin substituted ketones. A chelation-aided approach, which employs β-dichlorobutyltin substituted ketones and n-BuLi, is also useful for the generation of ketone α,β-dianions having the Z-geometry at the alkene. The generated dianions can be transformed into substituted ketones by reaction with various carbon electrophiles. 相似文献
90.
A series of cross-linking agents of varying rigidity and length were designed to stabilize helical structures in short peptides and were then synthesized. The sequences of the short peptides employed in this study each include two X residues (X=Dap, Dab, Orn, and Lys) at the i/i+4, i/i+7, or i/i+11 positions to provide the sites for cross-linking. These peptides were subjected to reaction with the synthesized cross-linking agents, and the helical content of the resulting cross-linked peptides were analyzed in detail by circular dichroism. For each of the peptide classes we found combinations with the cross-linking agents suitable for the construction of stable helical structures up to >95 % helicity at 5 degrees C. Our method could also be applied to biologically related sequences seen in native proteins such as Rev. 相似文献