全文获取类型
收费全文 | 529篇 |
免费 | 34篇 |
国内免费 | 4篇 |
专业分类
化学 | 448篇 |
晶体学 | 4篇 |
力学 | 3篇 |
数学 | 33篇 |
物理学 | 79篇 |
出版年
2023年 | 4篇 |
2022年 | 5篇 |
2021年 | 8篇 |
2020年 | 11篇 |
2019年 | 11篇 |
2018年 | 8篇 |
2017年 | 8篇 |
2016年 | 14篇 |
2015年 | 14篇 |
2014年 | 18篇 |
2013年 | 19篇 |
2012年 | 35篇 |
2011年 | 22篇 |
2010年 | 16篇 |
2009年 | 16篇 |
2008年 | 29篇 |
2007年 | 29篇 |
2006年 | 38篇 |
2005年 | 41篇 |
2004年 | 33篇 |
2003年 | 27篇 |
2002年 | 22篇 |
2001年 | 12篇 |
2000年 | 6篇 |
1999年 | 4篇 |
1998年 | 9篇 |
1997年 | 5篇 |
1996年 | 15篇 |
1995年 | 6篇 |
1994年 | 3篇 |
1993年 | 4篇 |
1992年 | 10篇 |
1991年 | 10篇 |
1990年 | 4篇 |
1988年 | 3篇 |
1987年 | 3篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1982年 | 3篇 |
1979年 | 2篇 |
1978年 | 5篇 |
1977年 | 5篇 |
1976年 | 4篇 |
1975年 | 2篇 |
1974年 | 7篇 |
1972年 | 2篇 |
1971年 | 3篇 |
1968年 | 1篇 |
1967年 | 1篇 |
1936年 | 1篇 |
排序方式: 共有567条查询结果,搜索用时 15 毫秒
91.
A Pd-catalyzed asymmetric synthesis of Si-stereogenic dibenzosiloles is developed through enantioselective C-H bond functionalization of prochiral 2-(arylsilyl)aryl triflates. High chemo- and enantioselectivities are achieved by employing a Josiphos-type ligand under mild conditions. 相似文献
92.
S Murayama B Su K Okabe A Kishimura K Osada M Miura T Funatsu K Kataoka M Kato 《Chemical communications (Cambridge, England)》2012,48(67):8380-8382
We developed a simple preparation procedure for the protein encapsulated nanoparticle and used the nanoparticle for spatiotemporal activity control of various proteins. We succeeded in the local protein activation within cells by light using the nanoparticle. 相似文献
93.
Enantioselective direct aldol reaction of α-substituted nitroacetates with aqueous formaldehyde for the synthesis of α-alkyl serines has been achieved under base-free neutral phase-transfer conditions with a bifunctional chiral phase-transfer catalyst. 相似文献
94.
Murashima K Watanabe T Kanegawa S Yoshihara D Inagaki Y Karasawa S Koga N 《Inorganic chemistry》2012,51(9):4982-4993
N,N-Dipyridilaminoxyl, NOpy(2), having a stable aminoxyl, was prepared as a new magnetic coupler for heterospin systems. Solutions of NOpy(2) were mixed with those of bis{1,1,1,5,5,5, hexafluoro-4-(phenylimino)-2-pentanonate}cobalt derivatives, Co(hfpip-X)(2), at a 1:1 ratio to afford the polymeric cobalt(II) complexes, [Co(hfpip-X)(2)(NOpy(2))](n); X = H (1), F (2), F(3) (3), F(5) (4), Cl (5), Cl(3) (6), Br (7), and I (8) as single crystals. In all complexes, the local structures of the cobalt-complex units were compressed octahedra and the pyridine ligands in NOpy(2) units coordinated to the cobalt ions in trans configuration to form linear chains for 1-4 and in cis configuration to form helical chains for 5-8. In the chains, the aminoxyl in NOpy(2) ferromagnetically interacted with the cobalt ions to produce the ferromagnetic chains with J(intra)/k(B) = 9-14 K. In the magnetic susceptibility experiments of aligned sample of 6, the magnetic easy axis was determined to be the a* axis, which was the direction perpendicular to the b axis of the chain axis. The resulting chains, all except 4, interacted antiferromagnetically among each other, and especially in 1, 5, 7, and 8, the magnetic behaviors characteristic to canted two-dimensional (2D) antiferromagnets with T(c) = 5.6, 4.0, 4.0, and 6.2 K, respectively, were observed. All complexes showed slow magnetic relaxations affected by the interchain antiferromagnetic interaction. The effective activation barriers, Δ(eff)/k(B), for the reorientation of the magnetism for all complexes except 4 were estimated to be 25-39 K in the presence of a direct current (dc) field. 相似文献
95.
A nonporous crystalline solid consisting of an organoarsenic platinum(II) complex, i.e., a mononuclear diiodoplatinum(II) complex trans-PtI(2)(cis-DHDAtBu)(2) (1) with cis-1,4-dihydro-1,4-dimethyl-2,3,5,6-tetrakis(tert-butoxycarbonyl)-1,4-diarsinine (cis-DHDAtBu), shows on-off solid-state luminescence switching through reversible solvent vapor uptake and escape. The on-off switching of solid-state luminescence was achieved without changing the structure or electronic state of the organoarsenic platinum(II) complex. 相似文献
96.
The reactions of N‐([1]benzofuro[3,2‐d]pyrimidin‐4‐yl)formamidines with hydroxylamine hydrochloride gave rearranged cyclization products via ring cleavage of the pyrimidine component accompanied by a ring closure of the 1,2,4‐oxadiazole to give N‐[2‐([1,2,4]oxadiazol‐5‐yl)[1]benzofuran‐3‐yl)formamide oximes. N‐([1]Benzothieno[3,2‐d]pyrimidin‐4‐yl)formamidines and N‐(pyrido[2,3‐d]pyrimidin‐4‐yl)formamidines with hydroxylamine hydrochloride gave similar results. 相似文献
97.
Takayuki Motoyama Toshiaki Hayashi Hiroshi Hirota Masashi Ueki Hiroyuki Osada 《Chemistry & biology》2012,19(12):1611-1619
Highlights? The terpendole biosynthetic gene cluster was isolated ? Terpendole E is a key biosynthetic intermediate of indole-diterpenes ? Terpendole E was overproduced by gene knockout of the bispecific enzyme TerP ? Indole-diterpene biosynthetic pathways can be classified into two groups 相似文献
98.
Kensuke Naka Shinsuke Inagi Yoshiki Chujo 《Macromolecular rapid communications》2006,27(24):2113-2117
Summary: The first π‐conjugated poly(thioketene dimer) was synthesized via the homopolymerization of a silylthioketene dimer by a chemical oxidation‐reduction process. The polymerization of trimethylsilylthioketene dimer in the presence of FeCl3 (in CHCl3 at 70 °C for 24 h) gave the corresponding doped poly(thioketene dimer). After treatment of the doped polymer with an aqueous solution of ammonia, the neutral poly(thioketene dimer) was obtained with an incidental desilylation. The polymer obtained was soluble in DMF and DMSO. From gel permeation chromatographic analysis (DMF, polystyrene standards), the number‐average molecular weight of the polymer was found to be 7 460. The polymer showed low oxidation potentials derived from the thioketene dimer unit. An effective extension of the π‐conjugation was observed in the polymer.
99.
Yoshiharu Kagami Jian Ping Gong Yoshihito Osada 《Macromolecular rapid communications》1996,17(8):539-543
Shape memory polymers were prepared by copolymerizing stearyl acrylate and methyl acrylate. The principle of this shape memory effect is based on reversible order-disorder transition of crystalline aggregates of stearyl moieties. A specific feature of this type of shape memory copolymer is that the transition temperature at which the polymer abruptly becomes soft and deforms can be controlled by changing the monomer composition, which enables one to adjust the shape memory effect at a desired temperature. Mechanism and process of the shape memory behaviors were discussed. 相似文献
100.
Tolerance bioaccumulation and biotransformation of arsenic compounds by a freshwater prawn (Macrobrachium rosenbergii) were investigated. M. rosenbergii was exposed to 10, 20, 30 and 35 μg As cm−3 of disodium arsenate [abbreviated as As(V)], 25, 50, 100 and 120 μg As cm−3 of methylarsonic acid (MMAA), or 100,200, 300 and 350 μg As cm−3 of dimethylarsinic acid (DMAA). Tolerances (50% lethal concentration: LC50) of the prawn against As(V), MMAA, and DMAA were 30, 100, and 300 μg As cm−3, respectively. The prawn accumulated arsenic compounds directly from aqueous phase and biotransformed them in part. Both methylation and demethylation of the arsenicals were observed in vivo. Highly methylated and less toxic arsenicals were less accumulated in M. rosenbergii. 相似文献