全文获取类型
收费全文 | 224篇 |
免费 | 8篇 |
国内免费 | 3篇 |
专业分类
化学 | 183篇 |
晶体学 | 2篇 |
力学 | 2篇 |
数学 | 19篇 |
物理学 | 29篇 |
出版年
2023年 | 2篇 |
2022年 | 3篇 |
2021年 | 3篇 |
2020年 | 3篇 |
2016年 | 1篇 |
2015年 | 6篇 |
2014年 | 11篇 |
2013年 | 11篇 |
2012年 | 16篇 |
2011年 | 16篇 |
2010年 | 8篇 |
2009年 | 7篇 |
2008年 | 10篇 |
2007年 | 12篇 |
2006年 | 13篇 |
2005年 | 16篇 |
2004年 | 9篇 |
2003年 | 12篇 |
2002年 | 5篇 |
2001年 | 5篇 |
2000年 | 1篇 |
1999年 | 3篇 |
1998年 | 1篇 |
1997年 | 4篇 |
1996年 | 1篇 |
1995年 | 4篇 |
1994年 | 1篇 |
1993年 | 4篇 |
1992年 | 3篇 |
1991年 | 2篇 |
1990年 | 3篇 |
1989年 | 3篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 1篇 |
1984年 | 1篇 |
1983年 | 2篇 |
1982年 | 1篇 |
1981年 | 2篇 |
1980年 | 4篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1977年 | 4篇 |
1976年 | 1篇 |
1975年 | 4篇 |
1974年 | 1篇 |
1973年 | 2篇 |
1969年 | 1篇 |
1967年 | 2篇 |
1966年 | 1篇 |
排序方式: 共有235条查询结果,搜索用时 15 毫秒
71.
Shigeyuki Yagi Ryuhei Yamada Norihiro Tsuji Shinji Murakami Toru Takagishi 《Supramolecular chemistry》2013,25(3):293-297
Abstract A porphyrin dimer with a polyether linkage was newly synthesized and its conformational change triggered by complexation with an sodium cation was examined. It was confirmed by 1H NMR titration experiments that the dimer bearing a pentaoxyehtylene linkage (1b) was effectively formed a 1:1 complex with a sodium perchlorate. A detailed investigation of the CIS values for the protons confirmed that the complex of 1b?Na+ adopts a slipped face-to-face conformation. 相似文献
72.
Ever since the raft model for biomembranes has been proposed, the traditional view of biomembranes based on the fluid-mosaic model has been altered. In the raft model, dynamical heterogeneities in multi-component lipid bilayers play an essential role. Focusing on the lateral phase separation of biomembranes and vesicles, we review some of the most relevant research conducted over the last decade. We mainly refer to those experimental works that are based on physical chemistry approach, and to theoretical explanations given in terms of soft matter physics. In the first part, we describe the phase behavior and the conformation of multi-component lipid bilayers. After formulating the hydrodynamics of fluid membranes in the presence of the surrounding solvent, we discuss the domain growth-law and decay rate of concentration fluctuations. Finally, we review several attempts to describe membrane rafts as two-dimensional microemulsion. 相似文献
73.
High‐Throughput Development of a Hybrid‐Type Fluorescent Glutamate Sensor for Analysis of Synaptic Transmission 下载免费PDF全文
Dr. Kenji Takikawa Dr. Daisuke Asanuma Dr. Shigeyuki Namiki Hirokazu Sakamoto Tetsuro Ariyoshi Naoya Kimpara Prof. Kenzo Hirose 《Angewandte Chemie (International ed. in English)》2014,53(49):13439-13443
Fluorescent sensors are powerful tools for visualizing cellular molecular dynamics. We present a high‐throughput screening system, designated hybrid‐type fluorescence indicator development (HyFInD), to identify optimal position‐specific fluorophore labeling in hybrid‐type sensors consisting of combinations of ligand‐binding protein mutants with small molecular fluorophores. We screened sensors for glutamate among hybrid molecules obtained by the reaction of four cysteine‐reactive fluorescence probes with a set of cysteine‐scanning mutants of the 274 amino acid S1S2 domain of AMPA‐type glutamate receptor GluA2 subunit. HyFInD identified a glutamate‐responsive probe (enhanced glutamate optical sensor: eEOS) with a dynamic range >2400 %, good photostability, and high selectivity. When eEOS was specifically tethered to neuronal surfaces, it reliably visualized the spatiotemporal dynamics of glutamate release at single synapses, revealing synapse‐to‐synapse heterogeneity of short‐term plasticity. 相似文献
74.
Shigeyuki Hanaoka Eiko Nagasawa Koji Nomura Masaru Yamazawa Mutsuo Ishizaki 《应用有机金属化学》2005,19(2):265-275
To elucidate the current extent of pollution of the environment with diphenylarsine chloride (DA, Clark I) and diphenylarsine cyanide (DC, Clark II), we have developed analytical procedures using gas and liquid chromatography and employed them to analyze water and soil samples. DA, DC, and their degradation products were extracted with water or organic solvents. Derivatization with n‐propanethiol was adopted to achieve higher analytical reproducibility. DA and DC were unstable and decomposed into bis(diphenylarsine)oxide (BDPAO) in water, but only negligibly into diphenylarsinic acid (DPAA) during the 30 days of a stability test. Diphenylarsenic compounds afforded the same product by this derivatization, but their reaction rates varied depending on the starting materials. DPAA had to be treated under acidic conditions at 60 °C to achieve the desired conversion efficiency. Recovery of the thiol derivatives of the diphenylarsenic compounds tested was almost quantitative from water, but only about 50% from soil, reflecting the low extraction efficiency. We applied the method to the analysis of organoarsenic compounds sampled from the water of the drinking well in Kamisu‐cho, Ibaraki Prefecture, where the water was thought to have had deleterious effects on the inhabitants. The high level of DPAA was identified as the causative agent. Our analyses of soil samples from Samukawa‐cho and Hiratsuka City, Kanagawa Prefecture, where a naval arsenal had previously stood, succeeded in identifying intact DA, BDPAO and triphenylarsine, diphenylarsenic thiol‐derivatives, as well as other substances (mustard gas, lewisite). The true magnitude of contamination became evident after these measurements. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
75.
Norio Ichinose Shigeyuki Yamada Nobuo Sakurai Toraya Fujiyama Naoko Masuda 《Fresenius' Journal of Analytical Chemistry》1978,293(1):23-24
Summary A new type of separation of phosphate ion, along with its spectrophotometric determination, was established by liquid-liquid extraction, where the yellow heteropoly acid formed by the reaction with ammonium molybdate in acid solution is quantitatively extracted into molten benzophenone at a temperature of about 60° C. When cooled down to room temperature, the benzophenone extract converts from the liquid state to the solid state. The resulting solidified extract is dissolved in methyl propionate, and the phosphate ion in the solvent is determined spectrophotometrically by the blue heteropoly acid method. Possible interference by Si, As and Ge is eliminated by the separation procedure.The authors wish to thank President Dr. Yawara Yoshitoshi and Prof. Yoshisaburo Ota of University School of Medicine, for their hospitality and encouragement. 相似文献
76.
Benzyl alpha,beta,beta-trifluoroacrylate (1) was prepared in good yield via the reductive Br-F elimination of benzyl 2-bromo-2,3,3,3-tetrafluoropropanoate or the palladium-catalyzed cross-coupling reaction of 1,2,2-trifluorovinylstannane with benzyl chloroformate. On treating 1 with various Grignard reagents or dialkylzinc reagents in the presence of copper(I) salt, the corresponding beta-substituted alpha,beta-difluoroacrylates were obtained in high yields with high Z-selectivity. Additionally, trialkylaluminum reagents were also found to be good nucleophiles, the corresponding addition-elimination products being afforded in good yields but with low stereoselectivity. 相似文献
77.
Nozawa D Okubo T Ishii T Chaki S Okuyama S Nakazato A 《Chemical & pharmaceutical bulletin》2007,55(7):1044-1050
While examining antagonists of the melanocortin-4 receptor (MC4 receptor), we found that compound 12b, containing a diphenylmethyl moiety, had a relatively high affinity for the MC4 receptor. When diphenylmethyl analogues were further examined, compounds 12c and 18 were also found to exhibit a high affinity for the MC4 receptor (IC(50)=46.7 nM and 33.2 nM, respectively). Furthermore, compound 12c was also found to show a high affinity for the serotonin transporter (IC(50)=10.7 nM). Here, we describe the synthesis and biological evaluation of various diphenylmethyl analogues in relation to their actions on the MC4 receptor and the serotonin transporter. 相似文献
78.
This paper presents a new method for making frit using soft-ferrite-based micro-magnetic particles (MMPs) in a micro-space, such as in a capillary tube. The MMPs-frit was made by injecting an aliquot of 10 microm (outer diameter; o.d.)-MMPs-suspension in methanol (ca. 1mg/ml) into a capillary tube (75 microm inner diameter (i.d.) x 375 microm o.d. x ca. 35 cm length) that was already sandwiched between a pair of cylindrical Neodium (Nd-Fe-B) magnets (1.5 mm o.d. x 1.5 mm height, 280 mT) at a position where the frit was made. The MMPs were trapped in the capillary tube as a frit due to the attraction of the magnets placed at surface on the capillary tube. With regard to durability, the frit was stable for methanol flow with a flow rate of 400 microl/min at room temperature. Using such a frit, a capillary column (20 cm long) was prepared by injecting a 5 microm (o.d.)-ODS-particle suspension in methanol (ca. 0.4 mg/microl) into the capillary tube. The MMPs-frits-ODS-packed column was stable for methanol for a flow pressure less than 20MPa. When comparing the present column with a conventional sintered-frits-ODS-packed column for the purposes of separating five kinds of biogenic amines by means of an on-column derivatization capillary electrochromatography (CEC), the performance of the MMPs-frits capillary column was almost equivalent to that of the sintered-frits-ODS-packed column. 相似文献
79.
Yamada S Takahashi T Konno T Ishihara T 《Chemical communications (Cambridge, England)》2007,(35):3679-3681
Fluorine-metal exchange reaction of 2,3,4,4,4-pentafluorocrotonates with organocuprate derived from Grignard reagent and CuCN takes place efficiently to generate the beta-metallated tetrafluorocrotonate intermediate, which reacts with various electrophiles to give beta-substituted 2,4,4,4-tetrafluorocrotonates. 相似文献
80.
Dr. Masaki Yoshida Dr. Mio Kondo Sena Torii Prof. Ken Sakai Prof. Shigeyuki Masaoka 《Angewandte Chemie (International ed. in English)》2015,54(27):7981-7984
Rational molecular design of catalytic systems capable of smooth O? O bond formation is critical to the development of efficient catalysts for water oxidation. A new ruthenium complex was developed, which bears pendant SO3? groups in the secondary coordination sphere: [Ru(terpy)(bpyms)(OH2)] (terpy=2,2′:6′,2′′‐terpyridine, bpyms=2,2′‐bipyridine‐5,5′‐bis(methanesulfonate)). Water oxidation driven by a Ce4+ oxidant is distinctly accelerated upon introduction of the pendant SO3? groups in comparisons to the parent catalyst, [Ru(terpy)(bpy)(OH2)]2+ (bpy=2,2′‐bipyridine). Spectroscopic, electrochemical, and crystallographic investigations concluded that the pendant SO3? groups promote the formation of an O? O bond via the secondary coordination sphere on the catalyst, whereas the influence of the pendant SO3? groups on the electronic structure of the [Ru(terpy)(bpy)(OH2)]2+ core is negligible. The results of this work indicate that modification of the secondary coordination sphere is a valuable strategy for the design of water oxidation catalysts. 相似文献