全文获取类型
收费全文 | 1789篇 |
免费 | 71篇 |
国内免费 | 19篇 |
专业分类
化学 | 1405篇 |
晶体学 | 28篇 |
力学 | 15篇 |
数学 | 86篇 |
物理学 | 345篇 |
出版年
2023年 | 10篇 |
2022年 | 8篇 |
2021年 | 21篇 |
2020年 | 23篇 |
2019年 | 32篇 |
2018年 | 26篇 |
2017年 | 19篇 |
2016年 | 40篇 |
2015年 | 41篇 |
2014年 | 43篇 |
2013年 | 68篇 |
2012年 | 117篇 |
2011年 | 127篇 |
2010年 | 77篇 |
2009年 | 66篇 |
2008年 | 83篇 |
2007年 | 109篇 |
2006年 | 108篇 |
2005年 | 90篇 |
2004年 | 75篇 |
2003年 | 98篇 |
2002年 | 87篇 |
2001年 | 47篇 |
2000年 | 39篇 |
1999年 | 31篇 |
1998年 | 16篇 |
1997年 | 20篇 |
1996年 | 24篇 |
1995年 | 17篇 |
1994年 | 24篇 |
1993年 | 15篇 |
1992年 | 19篇 |
1991年 | 15篇 |
1990年 | 14篇 |
1989年 | 10篇 |
1987年 | 14篇 |
1986年 | 16篇 |
1985年 | 28篇 |
1984年 | 29篇 |
1983年 | 12篇 |
1982年 | 16篇 |
1981年 | 12篇 |
1980年 | 10篇 |
1978年 | 14篇 |
1977年 | 14篇 |
1976年 | 6篇 |
1974年 | 5篇 |
1973年 | 6篇 |
1972年 | 9篇 |
1967年 | 5篇 |
排序方式: 共有1879条查询结果,搜索用时 15 毫秒
91.
Dr. Yusaku Nomura Dr. Frédéric Thuaud Dr. Daisuke Sekine Prof. Dr. Akihiro Ito Satoko Maeda Dr. Hiroyuki Koshino Dr. Daisuke Hashizume Dr. Atsuya Muranaka Dr. Thomas Cruchter Prof. Dr. Masanobu Uchiyama Prof. Dr. Satoshi Ichikawa Prof. Dr. Akira Matsuda Prof. Dr. Minoru Yoshida Prof. Dr. Go Hirai Prof. Dr. Mikiko Sodeoka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(35):8387-8392
A synthetic methodology to access all possible stereoisomers of spectomycin A1 (SMA1) and A2 (SMA2) has been established through late-stage diversification. The key reaction for the construction of all four diastereomers is an intramolecular cyclization based on the umpolung of π-allyl palladium species with bis(pinacolato)diborane (B2(pin)2). Silyl group assisted direct benzylic oxidation of each isomer enabled construction of the fragile β-hydroxytetralone skeleton to provide the SMAs. The relative and absolute stereochemistry of SMA2 was also determined, and the absolute stereochemistry of SMA1 was extrapolated based on the optical rotation of SMA2. The axial chirality of SMAs is discussed based on circular dichroism spectra and DFT calculations, and it is concluded that the M isomer is predominant in solution. Biochemical assessment of all isomers in vitro revealed that the C9 hydroxyl group and dimeric structure were both important for protein SUMOylation-inhibitory activity. 相似文献
92.
93.
Yoshihiro Ohta Makoto Karasawa Tetsurou Niiyama Akihiro Yokoyama Tsutomu Yokozawa 《Journal of polymer science. Part A, Polymer chemistry》2014,52(3):360-365
Well‐defined poly(3‐alkyl‐4‐benzamide) was synthesized by means of chain‐growth condensation polymerization of phenyl 3‐octyl‐4‐(4‐octyloxybenzyl(OOB)amino)benzoate ( 1c ) from initiator 2 , followed by removal of the OOB groups on amide nitrogen of poly 1c . Polymerization of 1c with phenyl 4‐(trifluoromethyl)benzoate ( 2b ) in the presence of 1,1,1,3,3,3‐hexamethyldisilazide (LiHMDS) and LiCl in THF at ?10 °C gave poly 1c with a narrow molecular weight distribution (Mw/Mn ≤ 1.08) and a well‐defined molecular weight (Mn = 4480–12,700) determined by the feed ratio of monomer to initiator (from 10 to 30). The OOB groups of poly 1c were removed with H2SO4 to give the corresponding N‐unsubstituted poly(p‐benzamide) (poly 1c′ ) with low polydispersity. The solublity of poly 1c′ in polar organic solvents was dramatically higher than that of poly(p‐benzamide), demonstrating that introduction of an alkyl group on the aromatic ring is very effective for improving the solubility of poly(p‐benzamide). © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 360–365 相似文献
94.
Yuki Sato Dr. Shin-ichi Kawaguchi Dr. Akihiro Nomoto Prof. Dr. Akiya Ogawa 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(9):2295-2302
Bis-phosphanated compounds are regarded as the most ubiquitous privileged ligand structures in transition-metal catalysis. The development of highly atom economical reactions is of great importance for their syntheses because less atom economical methods often require complicated purification procedures under inert atmospheres to remove excess starting materials and byproducts. Herein, the photoinduced addition reactions of diphosphane monosulfides bearing PV(S)−PIII single bonds to alkenes is disclosed. These reactions require only equimolar amounts of the diphosphane monosulfide relative to the alkene and facilitate highly selective introduction of two different types of phosphorus-containing groups, such as thiophosphoryl and phosphanyl groups, into a variety of alkenes without any catalyst, base, or additive. 相似文献
95.
Nickolaenko A. P. Galuk Yu. P. Hayakawa M. Kudintseva I. G. 《Radiophysics and Quantum Electronics》2021,64(6):401-411
Radiophysics and Quantum Electronics - We simulate numerically the propagation of slow-tail sferics, which occupy a wide frequency band from 1 Hz to 10 kHz, in the spherical Earth–ionosphere... 相似文献
96.
Dmitri V. Konarev Aleksey V. Kuzmin Salavat S. Khasanov Alexander F. Shestakov Akihiro Otsuka Hideki Yamochi Hiroshi Kitagawa Rimma N. Lyubovskaya 《化学:亚洲杂志》2020,15(17):2689-2695
Two salts of the aromatic hydrocarbon decacyclene, {cryptand[2.2.2](Cs+)} (decacyclene.?) ( 1 ) and {Bu3MeP+}(decacyclene.?) ( 2 ), were obtained. In both salts, decacyclene.? radical anions formed channels occupied by cations. However, corrugated hexagonal decacyclene.? layers could be outlined in the crystal structure of 1 with several side‐by‐side C???C approaches. The decacyclene.? radical anions showed strong distortion in both salts, deviating from the C3 symmetry owing to the repulsion of closely arranged hydrogen atoms and the Jahn‐Teller effect. Radical anions showed intense unusually low energy absorption in the IR‐range, with maxima at 4800 and 6000 cm?1. According to the carculations, these bands can originate from the SOMO‐LUMO+1 and SOMO‐LUMO+2 transitions, respectively. Radical anions exhibited a S=1/2 spin state, with an effective magnetic moment of 1.72 μB at 300 K. The decacyclene.? spin antiferromagnetically coupled with a Weiss temperature of ?11 K. Spin ordering was not observed down to 1.9 K owing to spin frustration in the hexagonal decacyclene.? layers. 相似文献
97.
In order to develop a new synthetic method and to study mechanism of oxidative polymerization of conducting polymers, polymerization of 3-octylthiophene in several organic solvents by γ-irradiation was examined. Polymers bimodal distribution with molecular weights at 500–1000 and 2000–3000 were generated by the irradiation of chloroform solutions. The values of monomer conversion (G(?M)) decreased from 445 to 10 with doses from 0.99 kGy to 594 kGy. The large G(?M) values and dose dependence of G(?M) cannot be explained with widely accepted mechanism for electrochemical polymerization or chemical oxidative polymerization. Another mechanism, which proceeds through chain reactions, is proposed. This mechanism explains the large G(?M) and the dependence on the dose. 相似文献
98.
Abstract The non-linear dielectric relaxation spectroscopy has been recently developed and applied to soft materials such as polymers. We have applied this new method to the S*C phases of some ferroelectric liquid crystals. Under a weak AC electric field, the original and third order harmonic frequency components of electric displacement are proportional to the first and third powers of the applied electric field, respectively. The linear spectrum obtained from the original frequency component shows the relaxation of Debye type and the third order non-linear spectrum shows the relaxation with an extended form of Debye type to the non-linear case. The third order non-linear dielectric increment is found to be negative, which implies that the dielectric non-linearity of the liquid crystal in the S*C phase is due to the saturation of molecular dipole moments induced by the applied electric field. The temperature dependence of the linear and third order non-linear spectra in the S*C phase are also studied. Both spectra do not change their forms much through the whole temperature range of the S*C phase. In the vicinity of the SA–S*C transition temperature, the critical behaviour is more remarkable in the third order spectrum than in the linear one. 相似文献
99.
Inside Back Cover: Carbon Dioxide to Methanol: The Aqueous Catalytic Way at Room Temperature (Chem. Eur. J. 44/2016)
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
100.