全文获取类型
收费全文 | 867篇 |
免费 | 14篇 |
国内免费 | 4篇 |
专业分类
化学 | 698篇 |
晶体学 | 3篇 |
力学 | 10篇 |
数学 | 51篇 |
物理学 | 123篇 |
出版年
2020年 | 7篇 |
2019年 | 10篇 |
2018年 | 5篇 |
2017年 | 3篇 |
2016年 | 9篇 |
2015年 | 7篇 |
2014年 | 10篇 |
2013年 | 45篇 |
2012年 | 38篇 |
2011年 | 30篇 |
2010年 | 20篇 |
2009年 | 14篇 |
2008年 | 29篇 |
2007年 | 45篇 |
2006年 | 56篇 |
2005年 | 41篇 |
2004年 | 48篇 |
2003年 | 40篇 |
2002年 | 50篇 |
2001年 | 19篇 |
2000年 | 11篇 |
1999年 | 8篇 |
1998年 | 13篇 |
1997年 | 9篇 |
1996年 | 49篇 |
1995年 | 11篇 |
1994年 | 10篇 |
1993年 | 10篇 |
1992年 | 7篇 |
1991年 | 10篇 |
1990年 | 12篇 |
1989年 | 6篇 |
1988年 | 10篇 |
1987年 | 7篇 |
1986年 | 10篇 |
1985年 | 21篇 |
1984年 | 18篇 |
1983年 | 7篇 |
1982年 | 17篇 |
1981年 | 18篇 |
1980年 | 17篇 |
1979年 | 16篇 |
1978年 | 10篇 |
1977年 | 7篇 |
1976年 | 10篇 |
1975年 | 8篇 |
1974年 | 5篇 |
1973年 | 4篇 |
1971年 | 3篇 |
1969年 | 6篇 |
排序方式: 共有885条查询结果,搜索用时 31 毫秒
101.
102.
Dr. Shintaro Ishida Dr. Takashi Abe Dr. Fumiya Hirakawa Tomoyuki Kosai Katsuhiro Sato Prof. Dr. Mitsuo Kira Prof. Dr. Takeaki Iwamoto 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(43):15100-15103
A persistent dialkylsilanone was synthesized by the dehydrobromination of a dialkylbromosilanol with tris(trimethylsilyl)silyl potassium in solution at ?80 °C: It was characterized by NMR and IR spectroscopy, and was tested in several reactions. In 29Si NMR spectrum in [D8]toluene, the signal due to the unsaturated silicon nuclei was observed at 128.7 ppm. Reactions of the dialkylsilanone with water and mesitonitrile oxide gave a silanediol and a [2+3] cycloadduct, respectively. The silanone remains intact in [D8]toluene below ?80 °C for at least two days, while it undergoes unprecedented isomerization to give a siloxysilene by means of 1,3‐silyl migration at higher temperatures. 相似文献
103.
Kana Nishimori Makoto Ouchi Mitsuo Sawamoto 《Macromolecular rapid communications》2016,37(17):1414-1420
A special initiator for metal‐catalyzed living radical polymerization facilitates sequence analyses by matrix‐assisted laser desorption/ionization time of flight mass spectrometry (MALDI‐TOF‐MS) of alternating copolymers from styrene and maleimide derivatives. The initiator is a malonate‐based alkyl halide (DEMM‐Br), in which two ester groups are attached on the carbon neighboring to bromide, and poor electron density of the radical species allows determination of next unit to the initiator in resultant alternating copolymers due to the selective initiation to styrene derivative. Thanks to the well‐defined α‐end group, sequence of the oligomeric products via radical copolymerization of PMS and EMI with DEMM‐Br can be more simply analyzed by MALDI‐TOF‐MS, and indeed the following are clarified: the crossover propagation is almost perfectly controlled regardless of the injection ratio; a minor error event of the disordered alternating sequence containing St–St sequential unit could take place; the minor error can be suppressed with an excess amount of maleimide.
104.
Toshio Aihara Wu-Shung Fu Mitsuo Hongoh Toshiyuki Shimoyama 《Experimental Thermal and Fluid Science》1990,3(6):623-631
An experimental study was made on convective heat and mass transfer from a horizontal heated cylinder in a downward flow of air-water mist at a blockage ratio of 0.4. The measured local heat transfer coefficients agree fairly well with the authors' numerical solutions obtained previously for the front surface of a cylinder over the ranges mass flow ratio 0–4.5×10−2, a temperature difference between the cylinder and air 10–43 K, gas Reynolds number (7.9–23)×103, Rosin-Rammler size parameter 105–168 μm, and dispersion parameter 3.4–3.7. Heat transfer augmentation, two-pahse to single-phase of greater than 19 was attained at the forward stagnation point. For heat transfer in the rear part of the cylinder, an empirical formula is derived by taking into account the dimensionless governing variables, that is, coolant-feed and evaporation parameters. 相似文献
105.
Toshiyuki Fujii Genki Okude Akihiro Uehara Shun Sekimoto Hirokazu Hayashi Mitsuo Akabori Kazuo Minato Hajimu Yamana 《Journal of Radioanalytical and Nuclear Chemistry》2011,288(1):181-187
Distribution behavior of Ce(III), Am(III), and Cm(III) between tri-n-butyl phosphate solution and molten calcium nitrate hydrate Ca(NO3)2·RH2O or molten calcium chloride hydrate CaCl2·RH2O was studied radiochemically. In Ca(NO3)2·RH2O systems, maximum separation factors of Ce and Cm to Am were observed to be 12 (Ce/Am) and 1.7 (Cm/Am). The distribution
ratios of these elements increased with the decrease of water activity in the hydrates, and the extractabilities at the water
deficient region was less sensitive compared to those at the water abundant region. This trend was similar to the coordination
circumstance change observed in electronic absorption spectra of Nd(III) in the hydrates. 相似文献
106.
Paulovich FV Moraes ML Maki RM Ferreira M Oliveira ON de Oliveira MC 《The Analyst》2011,136(7):1344-1350
The development of new methods and concepts to visualize massive amounts of data holds the promise to revolutionize the way scientific results are analyzed, especially when tasks such as classification and clustering are involved, as in the case of sensing and biosensing. In this paper we employ a suite of software tools, referred to as PEx-Sensors, through which projection techniques are used to analyze electrical impedance spectroscopy data in electronic tongues and related sensors. The possibility of treating high dimension datasets with PEx-Sensors is advantageous because the whole impedance vs. frequency curves obtained with various sensing units and for a variety of samples can be analyzed at once. It will be shown that non-linear projection techniques such as Sammon's Mapping or IDMAP provide higher distinction ability than linear methods for sensor arrays containing units capable of molecular recognition, apparently because these techniques are able to capture the cooperative response owing to specific interactions between the sensing unit material and the analyte. In addition to allowing for a higher sensitivity and selectivity, the use of PEx-Sensors permits the identification of the major contributors for the distinguishing ability of sensing units and of the optimized frequency range. The latter will be illustrated with sensing units made with layer-by-layer (LbL) films to detect phytic acid, whose capacitance data were visualized with Parallel Coordinates. Significantly, the implementation of PEx-Sensors was conceived so as to handle any type of sensor based on any type of principle of detection, representing therefore a generic platform for treating large amounts of data for sensors and biosensors. 相似文献
107.
Makoto Obata Yurie Tanaka Naoko Araki Shiho Hirohara Shigenobu Yano Kazunori Mitsuo Keisuke Asai Masafumi Harada Toyoji Kakuchi Chikara Ohtsuki 《Journal of polymer science. Part A, Polymer chemistry》2005,43(14):2997-3006
Pressure‐sensitive paint (PSP), which consists of luminescent molecules embedded in an oxygen‐permeable polymer, has been developed for use in wind‐tunnel experiments. To improve the PSP technique, a novel luminescent methacrylate monomer, 5‐[4‐(2‐methacryloyloxyethoxycarbonyl)phenyl]‐10,15,20‐triphenylporphinato platinum(II), was synthesized and copolymerized with isobutyl methacrylate and 2,2,2‐trifluoroethyl methacrylate to produce a dye‐pendant copolymer ( 2 ). The introduction of 5,10,15,20‐tetraphenylporphinato platinum(II) (PtTPP) dye into 2 was confirmed by ultraviolet–visible spectroscopy and extended X‐ray absorption fine structure measurements. The extent of PtTPP dye incorporation in 2 was proportional to the molar fraction of the PtTPP‐pendant methacrylate monomer in the feed. The oxygen‐sensing property of 2 was compared with that of a PSP consisting of PtTPP dye embedded in poly(isobutyl‐co‐2,2,2‐trifluoroethyl methacrylate). Although the simple mixture of PtTPP and poly(isobutyl‐co‐2,2,2‐trifluoroethyl methacrylate) showed a marked deviation from a single Stern–Volmer relation, novel copolymer 2 gave a highly linear Stern–Volmer plot. This was unequivocal evidence of dye conjugation on the oxygen‐sensing polymer film. © 2005Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2997–3006, 2005 相似文献
108.
Masami Kamigaito Mitsuo Sawamoto Toshinobu Higashimura 《Journal of polymer science. Part A, Polymer chemistry》1993,31(12):2987-2994
Phosphoric and phosphinic acid derivatives (R1R2PO2H; R1, R2 = OPh, OPh; OnBu, OnBu; Ph, Ph; Ph, H) in conjunction with zinc chloride (ZnCl2) led to living cationic polymerization of isobutyl vinyl ether (IBVE) in toluene below 0°C. The number-average molecular weights (M?n) of the polymers (M?n > 2 × 104) were directly proportional to monomer conversion and in excellent agreement with the calculated values assuming that one polymer chain forms per R1R2PO2H molecule. Throughout the reaction, the molecular weight distributions (MWDs) stayed narrow (M?w/M?n ? 1.1). A dibasic acid, PhOP (O) (OH)2, coupled with ZnCl2, also induced living cationic polymerization of IBVE where one molecule of the acid generated two living polymer chains. The polymerization by (PhO)2PO2H/ZnCl2 and its model reactions were directly analyzed by 31P and 1H-NMR spectroscopy. The analysis showed that the acid initially forms the adduct [CH3CH(OiBu)OP(O)(OPh)2], the phosphate linkage of which is in turn activated by ZnCl2 so as to initiate living propagation. The finding thus indicates that (PhO)2PO2H indeed acts as an initiator in the living polymerization. The NMR analysis also suggested that an exchange reaction occurs between the phosphate group at the polymer terminal and the chlorine in ZnCl2. The occurrence of living IBVE polymerization with these various R1R2PO2H/ZnCl2 systems shows that phosphoric and phosphinic acids are another general class of protonic acids which are effective initiators for the living cationic polymerization assisted by Lewis acids. © 1993 John Wiley & Sons, Inc. 相似文献
109.
110.