全文获取类型
收费全文 | 343篇 |
免费 | 15篇 |
国内免费 | 1篇 |
专业分类
化学 | 238篇 |
晶体学 | 8篇 |
力学 | 5篇 |
数学 | 26篇 |
物理学 | 82篇 |
出版年
2023年 | 1篇 |
2021年 | 5篇 |
2020年 | 9篇 |
2019年 | 7篇 |
2018年 | 2篇 |
2017年 | 2篇 |
2016年 | 13篇 |
2015年 | 4篇 |
2014年 | 9篇 |
2013年 | 14篇 |
2012年 | 20篇 |
2011年 | 23篇 |
2010年 | 13篇 |
2009年 | 14篇 |
2008年 | 23篇 |
2007年 | 27篇 |
2006年 | 28篇 |
2005年 | 15篇 |
2004年 | 16篇 |
2003年 | 12篇 |
2002年 | 9篇 |
2001年 | 7篇 |
2000年 | 6篇 |
1999年 | 7篇 |
1998年 | 3篇 |
1997年 | 6篇 |
1996年 | 7篇 |
1995年 | 4篇 |
1994年 | 10篇 |
1993年 | 5篇 |
1992年 | 9篇 |
1991年 | 3篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 2篇 |
1985年 | 4篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1980年 | 1篇 |
1979年 | 2篇 |
1978年 | 1篇 |
1976年 | 1篇 |
1975年 | 2篇 |
1974年 | 1篇 |
1973年 | 1篇 |
1970年 | 1篇 |
1968年 | 1篇 |
1959年 | 1篇 |
排序方式: 共有359条查询结果,搜索用时 31 毫秒
101.
Although three dimensional (3D) solvation structure is much more informative than one dimensional structure, its evaluation is difficult experimentally and theoretically. In our previous Communication [Yokogawa et al., J. Chem. Phys. 123, 211102 (2005)], we proposed a new method to present reconstructed spatial distribution function (RC-SDF) from a set of radial distribution functions (RDFs). In this article, we successfully extended the method more accurately with new basis sets. This new method was applied to two liquid solvation structures, methanol and dimethyl sulfoxide, as examples. Their RC-SDFs evaluated here clearly show that the former solvation structure is well defined while the latter one is broad, which agrees well with the SDFs calculated directly from molecular dynamics simulations. These results indicate that the method can reproduce well these 3D solvation structures in reasonable computational cost. 相似文献
102.
Mitsushiro Nomura Souichi Sakaki Yoshimasa Hoshino 《Journal of organometallic chemistry》2006,691(15):3274-3284
The one-pot reaction of [Cp∗Mo(NO)(CO)2] with elemental sulfur and dimethyl acetylenedicarboxylate (C2Z2 (Z = COOMe)) gave the [2+2] cycloadduct of the mononuclear molybdenum dithiolene complex [Cp∗Mo(NO)(S2C2Z2)(C2Z2)] (1), and some binuclear complexes:[Cp∗Mo(NO)(S2C2Z2)]2 (2), [Cp∗2Mo2(NO)2S2(S2C2Z2)] (3) and [Cp∗Mo(NO)S2]2 (4).The reaction of [Cp∗Mo(NO)(Cl)(μ-Cl)]2 with OC{S2C2(COOMe)2} in the presence of sodium methoxide also produced complex 2 and the paramagnetic Cp∗Mo bisdithiolene complex [Cp∗Mo(S2C2Z2)2] (5, Z = COOMe).The structures of complexes 1-5 were determined by X-ray crystal structure analysis.The nitrosyl ligands of complexes 1-4 showed a linear coordination to the molybdenum center (the Mo-N-O bond angles = 169-174°), and their N-O bond lengths were 1.17-1.20 Å.In the binuclear complexes 2-4, two nitrosyl ligands were placed at cis-position.Complexes 1 and 2 were characterized by cyclic voltammetry and spectroelectrochemistry (visible and IR). The electrochemical reduction of the dimeric complex 2 formed the monomeric dithiolene complex[Cp∗Mo(NO)(S2C2Z2)]− (X−) whose lifetime was several minutes. When the anion X− was electrochemically oxidized, the coordinatively unsaturated species X was generated, but it was immediately dimerized to afford the original dimeric complex 2. The reduction of the complex 1 included the elimination of the bridged DMAD moiety (C2Z2) to give the anion X−. 相似文献
103.
Higuchi R Inoue S Inagaki K Sakai M Miyamoto T Komori T Inagaki M Isobe R 《Chemical & pharmaceutical bulletin》2006,54(3):287-291
A ganglioside molecular species GP-3 (1) has been obtained from the water-soluble lipid fraction of the chloroform/methanol extract of the starfish Asterina pectinifera. The structure of the ganglioside has been determined on the basis of chemical and spectroscopic evidence. Compound 1 represents new ganglioside molecular species possessing two moles of sialic acids at the inner part of the sugar moiety. Partial hydrolysis by hot water and an enzymatic hydrolysis by means of endoglycoceramidase (EGCase) have proved useful for structure elucidation of the complex oligosaccharide moiety. Moreover, 1 exhibits neuritogenic activity toward the rat pheochromocytoma cell line, PC-12 cells, in the presence of nerve growth factor (NGF). 相似文献
104.
[Structure: see text] A total synthesis of PD 113,271, an antitumor fostriecin analogue isolated from Streptomyces pulveraceus, was achieved by the chiral pool approach starting with D-galactose and L-tartaric acid. The synthesis of PD 113,271 led to unambiguous assignment of the relative and absolute stereochemistry of its stereocenters. 相似文献
105.
Let R = K[x
1, x
2, x
3, x
4] be the polynomial ring over a field of characteristic zero. For the ideal (x1a, x2b, x3c, x4d) ì R{(x_1^a, x_2^b, x_3^c, x_4^d) \subset R}, where at least one of a, b, c and d is equal to two, we prove that its generic initial ideal with respect to the reverse lexicographic order is the almost revlex
ideal corresponding to the same Hilbert function. 相似文献
106.
In this paper, we discuss with guaranteed a priori and a posteriori error estimates of finite element approximations for not necessarily coercive linear second order Dirichlet problems. Here, ‘guaranteed’ means we can get the error bounds in which all constants included are explicitly given or represented as a numerically computable form. Using the invertibility condition of concerning elliptic operator, guaranteed a priori and a posteriori error estimates are formulated. This kind of estimates plays essential and important roles in the numerical verification of solutions for nonlinear elliptic problems. Several numerical examples that confirm the actual effectiveness of the method are presented. 相似文献
107.
108.
Jyunichi Koyanagi Katsumi Yamamoto Kouji Nakayama Akira Tanaka 《Journal of heterocyclic chemistry》1994,31(4):1093-1095
4-endo-5-exo-Dibromo-3-methyl-3,6-endo-oxyperhydrophthalic anhydride 3b and 4-exo-5-endo-dibro-mo-3-methyl-3,6-endo-oxyperhydrophtbalic anhydride 3c were isolated from the bromo-adducts of 3-methyl-3,6-endo-oxy-1,2,3,6-tetrahydrophthalic anhydride 2. When 3b or 3c was heated in quinoline, only 3-bromo-2-methylfuran 4 was obtained from 3b and only 4-bromo-2-methylfuran 5 from 3c. 相似文献
109.
Momoko Kumemura Dominique Collard Christophe Yamahata Naoyoshi Sakaki Gen Hashiguchi Hiroyuki Fujita 《Chemphyschem》2007,8(12):1875-1880
This paper presents a systematic method to isolate and trap long single DNA segments between integrated electrodes in a microfluidic environment. Double stranded lambda-DNA molecules are introduced in a microchip and are isolated by electrophoretic force through microfluidic channels. Downstream, each individual molecule is extended and oriented by ac dielectrophoresis (900 kHz, 1 MV m(-1)) and anchored between aluminium electrodes. With a proper design, a long DNA segment (up to 10 microm) can be instantly captured in stretched conformation, opening way for further assays. 相似文献
110.
Toru Sakaki Takaaki Harada Gang Deng Hirosuke Kawabata Yohko Kawahara Seiji Shinkai 《Journal of inclusion phenomena and macrocyclic chemistry》1992,14(3-4):285-302
In order to obtain insights into relationships between the calix[4]arene structure and the ion selectivity in the electrode system, 20 ionophoric calix[4]arenes were synthesized and their ion selectivity (with Na+ as a standard) estimated. Among these ionophoric calix[4]arenes, 25,26,27,28-tetrakis[(ethoxycarbonyl)methoxy]-p-t-octylcalix[4]arene afforded the highest logK
NA,M
pot
value (–3.1) in the presence of 2-fluorophenyl-2-nitrophenylether (10) as the best of 13 plasticizers. This is the first example in which the Na+/K+ selectivity exceeds a factor of 103 in the electrode system based on the neutral carrier. The high Na+ selectivity is attributed to modification of the upper rim which ostensibly has no relation with the component of the cavity. This paper demonstrates the potential relationships between the unique structure of the calix[4]arene-based ligands and selectivity performance for the design of ion-selective electrodes. 相似文献