全文获取类型
收费全文 | 1322篇 |
免费 | 29篇 |
国内免费 | 9篇 |
专业分类
化学 | 965篇 |
晶体学 | 11篇 |
力学 | 23篇 |
数学 | 62篇 |
物理学 | 299篇 |
出版年
2021年 | 8篇 |
2020年 | 8篇 |
2019年 | 12篇 |
2018年 | 10篇 |
2016年 | 16篇 |
2015年 | 30篇 |
2014年 | 21篇 |
2013年 | 56篇 |
2012年 | 46篇 |
2011年 | 48篇 |
2010年 | 47篇 |
2009年 | 28篇 |
2008年 | 67篇 |
2007年 | 63篇 |
2006年 | 48篇 |
2005年 | 51篇 |
2004年 | 45篇 |
2003年 | 48篇 |
2002年 | 43篇 |
2001年 | 30篇 |
2000年 | 42篇 |
1999年 | 17篇 |
1998年 | 9篇 |
1997年 | 14篇 |
1996年 | 14篇 |
1995年 | 12篇 |
1994年 | 17篇 |
1993年 | 9篇 |
1992年 | 16篇 |
1991年 | 13篇 |
1990年 | 18篇 |
1989年 | 29篇 |
1988年 | 26篇 |
1987年 | 14篇 |
1986年 | 19篇 |
1985年 | 43篇 |
1984年 | 24篇 |
1983年 | 17篇 |
1982年 | 23篇 |
1981年 | 30篇 |
1980年 | 22篇 |
1979年 | 25篇 |
1978年 | 20篇 |
1977年 | 23篇 |
1976年 | 30篇 |
1975年 | 31篇 |
1974年 | 19篇 |
1973年 | 11篇 |
1969年 | 6篇 |
1967年 | 5篇 |
排序方式: 共有1360条查询结果,搜索用时 93 毫秒
61.
Shinji Ejiri Sinya Aoki Tetsuo Hatsuda Kazuyuki Kanaya Yoshiyuki Nakagawa Hiroshi Ohno Hana Saito Takashi Umeda 《Central European Journal of Physics》2012,10(6):1322-1325
We study the QCD phase structure at high temperature and density adopting a histogram method. Because the quark determinant is complex at finite density, the Monte-Carlo method cannot be applied directly. We use a reweighting method and try to solve the problems which arise in the reweighting method, i.e. the sign problem and the overlap problem. We discuss the chemical potential dependence of the probability distribution function in the heavy quark mass region and examine the applicability of the approach in the light quark region. 相似文献
62.
Makoto Nonomura Fumio Nakagawa Shinya Mizusawa Takashi Ohno Hiroyuki Kobayashi Toshiyuki Hobo 《International journal of environmental analytical chemistry》2013,93(4):371-379
Abstract Although cyanide compounds are not incorporated in photographic processing solutions, false detection of cyanide ion is often encountered during the determination of total cyanide by various standardized methods such as ISO, ANSI and JIS. Various organic compounds and nitrogen compounds in the processing solutions were examined because of this false detection. The results suggest that hydrogen cyanide is formed by a reaction between these compounds during the distillation process for the separation of total cyanide, even though ISO, ANSI and JIS were used. The results support the following three mechanisms of cyanide formation involved in the process: (1) Hydroxylammonium salts reacts with another ingredient, formaldehyde, to form formaldoxime, which then decomposes to HCN. (2) Hydroxylammonium is oxidized by air to form nitrite ion, which subsequently reacts with organic compounds such as aminocarboxylic acids and aromatic amines (the colour-developing agent) to form HCN. (3) Potassium permanganate oxidizes aromatic amines to form HCN. 相似文献
63.
64.
Abstract Color centers in rutile-structured MgF2 single crystals irradiated at 20K/360K by reactor neutrons are investigated spectroscopically at LNT. Four different types of the F-F vacancy bond in MgF2 are possibly identified to the observed absorption bands as due to the F2 centers; instead of previous assignments, the 300nm band to the F2(D2h), the 325nm band to the F2(C1), the 355nm band to the F2(C2v), and the 400nm band to the F2(C2h) centers. 相似文献
65.
Manabu Ishifune Ryuhei Suzuki Mikio Yamane Hiroyuki Tanabe Yuki Nakagawa Kumao Uchida 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(7):523-528
Acrylamide (AAm) was found to polymerize in a solution of poly(N‐isopropylacrylamide) (PNIPAAm) in water at around its lower critical solution temperature (LCST) (32°C) without any initiators. This phenomenon was specifically observed in aqueous solutions of the polymers having LCST such as PNIPAAm and poly(methylvinylether) (PMVE). AAm polymerized only when PNIPAAm and AAm were dissolved in water below LCST of PNIPAAm and then the solution was warmed up to the polymerization temperature (40°C). On the other hand, the polymerization of AAm did not proceed when AAm was added into aqueous PNIPAAm solution during and after the phase separation above 32°C. Furthermore the polymerizability of AAm was remarkably affected by the concentration and molecular weight of the PNIPAAm additives. Under the condition of lower PNIPAAm concentration (0.30 mol/L), the increase in the molecular weight of PNIPAAm considerably increased the molecular weight of the resulting PAAm but decreased the yield of PAAm. Under the condition of higher PNIPAAm concentration (0.60 mol/L) the polymerizability was not so affected by the molecular weight of PNIPAAm, while the molecular weight of PAAm formed by using higher molecular weight PNIPAAm was higher than those of PAAm formed by using lower molecular weight PNIPAAm. Moreover, the molecular weight of PAAm formed by the PNIPAAm induced polymerization of AAm was much higher than that of the polymer obtained by the radical polymerization using AIBN in THF or VA‐ 061 in water. 相似文献
66.
Atsushi Kubono Kazuki Yoshino Toshiro Ninomiya Ryuichi Akiyama Katsufumi Tanaka 《Liquid crystals》2013,40(8):1089-1095
The visco-elastic properties for binary mixtures of 4-n -hexyloxy-4′-cyanobiphenyl (6OCB) and 4-n-octyloxy-4′-cyanobiphenyl (8OCB) are investigated in detail by a light scattering technique. The mixtures exhibit a reentrant nematic (RN) phase between the smectic A (SmA) and crystal phases in the range 22.0–29.5 wt % of 6OCB. The viscosity and the elastic constant increase with cooling in both the nematic and reentrant nematic phases. It is also found that the mixtures exhibit anomalously large values of viscosity and elastic constant near the phase transition, i.e. a pretransitional phenomenon can be observed. The activation energy for viscosity is smaller in the RN phase than in the ordinary nematic phase appearing at higher temperatures, while the normalized elastic constant (defined as the ratio of the elastic constant to the square of the dielectric anisotropy) is larger. Moreover, the visco-elastic behaviour depends on the specific time during which the sample has been kept in the SmA phase. These results confirm that the SmA phase has a strong influence on the formation of molecular aggregates, which plays an important role in the reentrant phenomenon of these systems. 相似文献
67.
Dr. Yu Nakagawa Takashi Doi Takara Taketani Prof. K. Takegoshi Prof. Yasuhiro Igarashi Dr. Yukishige Ito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(32):10516-10525
Pradimicins (PRMs) and benanomicins are the only family of non‐peptidic natural products with lectin‐like properties, that is, they recognize D ‐mannopyranoside (Man) in the presence of Ca2+ ions. Coupled with their unique Man binding ability, they exhibit antifungal and anti‐HIV activities through binding to Man‐containing glycans of pathogens. Notwithstanding the great potential of PRMs as the lectin mimics and therapeutic leads, their molecular basis of Man recognition has yet to be established. Their aggregate‐forming propensity has impeded conventional interaction analysis in solution, and the analytical difficulty is exacerbated by the existence of two Man binding sites in PRMs. In this work, we investigated the geometry of the primary Man binding of PRM‐A, an original member of PRMs, by the recently developed analytical strategy using the solid aggregate composed of the 1:1 complex of PRM‐A and Man. Evaluation of intermolecular distances by solid‐state NMR spectroscopy revealed that the C2–C4 region of Man is in close contact with the primary binding site of PRM‐A, while the C1 and C6 positions of Man are relatively distant. The binding geometry was further validated by co‐precipitation experiments using deoxy‐Man derivatives, leading to the proposal that PRM‐A binds not only to terminal Man residues at the non‐reducing end of glycans, but also to internal 6‐substituted Man residues. The present study provides new insights into the molecular basis of Man recognition and glycan specificity of PRM‐A. 相似文献
68.
Dr. Ryu Yamasaki Dr. Masato Ohashi Kyotaro Maeda Takuya Kitamura Minami Nakagawa Korehito Kato Tetsushi Fujita Ryohei Kamura Kazuto Kinoshita Dr. Hyuma Masu Prof. Dr. Isao Azumaya Prof. Dr. Sensuke Ogoshi Prof. Dr. Shinichi Saito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(10):3415-3425
A detailed study of the Ni‐catalyzed [4+3+2] cycloaddition reaction between ethyl cyclopropylideneacetate and dienynes has been conducted, resulting in the development of a new method for the synthesis of compounds containing nine‐membered rings. We studied the reactivity of various dienynes, together with their substituent and conformational effects. The mechanism of the reaction was probed by examining the stoichiometric reactions of the Ni complexes and dienynes. 相似文献
69.
Miho Kusakari Yurie OhtaHideaki Nakagawa Hiroshi KatagiriTatsuro Kijima Satoshi MurakamiShigeru Matsuba Bunpei Hatano 《Tetrahedron letters》2014
An enantioresolution of 2-methoxy-2-(1-naphtyl)propionic acid (MαNP acid) using the diastereomeric salt with chiral (R)-phenylethylamine was achieved to give enantiopure (R)-MαNP acid in 29% yield with >99% ee based on rac-MαNP acid. X-ray crystallographic analysis of diastereomeric salt revealed that (R)-MαNP acid was tightly arranged by four independent hydrogen bonds and one CH–π interaction with (R)-phenylethylamine. 相似文献
70.
H. Kuboki H. Okuno A. Hershcovitch T. Dantsuka H. Hasebe K. Ikegami H. Imao O. Kamigaito M. Kase T. Maie T. Nakagawa Y. Yano 《Journal of Radioanalytical and Nuclear Chemistry》2014,299(2):1029-1034
A differential pumping system with a Plasma Window (PW) has been developed for an application to a window-less He gas charge stripper. A PW with Southern Methodist University design was newly fabricated and tested off-line for evaluation of differential pumping efficiency. Switching gases for plasma seed from Ar to He was tested. It was found that the PW reduced the pressure at the first differential pumping section to 1/13 for Ar and to 1/17 for He, comparing with differential pumping without PW. At the second pumping section, the pressures were drastically reduced to 1/160 and to 1/4,520 for Ar and He, respectively. These pressure reduction factors indicate that one differentially pumped stage could be removed from a conventional differential pumping system. 相似文献