全文获取类型
收费全文 | 82篇 |
免费 | 1篇 |
国内免费 | 17篇 |
专业分类
化学 | 95篇 |
物理学 | 5篇 |
出版年
2023年 | 3篇 |
2022年 | 1篇 |
2021年 | 1篇 |
2020年 | 1篇 |
2019年 | 1篇 |
2016年 | 1篇 |
2015年 | 2篇 |
2014年 | 2篇 |
2013年 | 10篇 |
2012年 | 2篇 |
2011年 | 6篇 |
2010年 | 6篇 |
2009年 | 6篇 |
2008年 | 5篇 |
2007年 | 4篇 |
2006年 | 5篇 |
2005年 | 10篇 |
2004年 | 4篇 |
2003年 | 1篇 |
2002年 | 1篇 |
2000年 | 1篇 |
1998年 | 1篇 |
1997年 | 6篇 |
1996年 | 4篇 |
1995年 | 2篇 |
1994年 | 3篇 |
1993年 | 2篇 |
1992年 | 4篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1989年 | 2篇 |
1986年 | 1篇 |
排序方式: 共有100条查询结果,搜索用时 0 毫秒
61.
62.
Metalation of (RSiMe2)3CH (1a R = H, 1b R = Me, 1c R = Ph) with lithium diisopropylamide (LDA) or methyllithium in THF gave organolithium reagents (RSiMe2)3CLi, which reacted with the formylated calixarene (2), to give the corresponding 5,17-bis[2,2-bis(organosilyl)-1-ethenyl]-25,26,27,28-tetrapropoxycalix[4]arenes (3a, 3b and 3c) via the Peterson olefination. The compounds (RSiMe2)3CLi were treated with 25,26,27,28-tetrakis(4-bromobutoxy)calix[4]arene (4) to give 25,26,27,28-tetrakis[4-(tris(dimethylsilyl)methyl)butoxy] calix[4]arene (5a) and 25,26,27,28-tetrakis[4-(tris(trimethylsilyl)methyl)butoxy] calix[4]arene (5b) via nucleophilic substitution reactions. However the compound 25,26,27,28-tetrakis[4-(tris(dimethylphenylsilyl)methyl)butoxy] calix[4]arene (5c) was not obtained, presumably because (PhSiMe2)3C- is highly sterically hindered and the reactivity of its derivatives is low. The compound 5a has potential as a core for dendrimers. 相似文献
63.
Dengxu Wang 《Journal of organometallic chemistry》2010,695(21):2329-2337
A series of novel tetrahedral silicon-centered imidazolyl derivatives, Bis(4-(imidazol-1-yl)phenyl)dimethylsilane (1), Tri(4-(imidazol-1-yl)phenyl)methyl silane (2), Bis(4-(imidazol-1-yl)phenyl)diphenylsilane (3), Tri(4-(imidazol-1-yl)phenyl)phenylsilane (4), [Bis(4-(imidazol-1-yl)phenyl)](4-bromophenyl)phenylsilane (5) and [Tri(4-(imidazol-1-yl)phenyl)](4-bromophenyl)silane (6) have been synthesized and characterized by FTIR, 1H NMR, 13C NMR and mass spectroscopy. They all display high thermal stability, are fluorescent with emission in the region of violet to blue, and possess large HOMO-LUMO energy gaps ranging from 4.9585 to 5.1879 eV, which could be potentially used as blue emitters or hole blocking materials in OLEDs. Moreover, the metal ion titrations based on Ag (I) and compounds 1-4 reveal that these ligands show distinguishable fluorescence response with increasing of Ag (I) ions. 相似文献
64.
Shinobu Tsutsui Hiromasa Tanaka Shigeki Matsumoto 《Journal of organometallic chemistry》2006,691(7):1341-1346
A lattice-framework silanone, a racemate of (4R,6R)- and (4S,6S)-2,3,4,6,7,8-hexa-tert-butyl-1,5-disilatricyclo[4.2.0.01,4]octa-2,7-dien-5-one (4), was generated by the photoreaction of the corresponding lattice-framework disilene, a racemate of (4R,6R,4′R,6′R)- and (4S,6S,4′S,6′S)-2,3,4,6,7,8,2′,3′,4′,6′,7′,8′-dodeca-tert-butyl-[5,5′]bi{1,5-disilatricyclo[4.2.0.01,4]octylidene}-2,7,2′,7′-tetraene (dl-1), with mesitonitrile oxide. The silanone 4 was dimerized to produce a mixture of the corresponding dl- and meso-1,3-dioxa-2,4-disiletane derivatives 2. DFT calculations suggested that the non-selective dimerization of 4 to 2 is attributed to the irreversibility of the reaction. 相似文献
65.
Zhonghua Li Xiuyan Song 《Phosphorus, sulfur, and silicon and the related elements》2013,188(7):1411-1416
Ten 1-(O,O-dialkyl phosphorylamido)propyl-5-aza-2,8,9-trioxa-1-silatricyclo [3,3,3,01,5] undecanes were synthesized by the reaction of dialkoxy phosphoryl chlorides with aminopropyl silatrane and their structures were established by elemental analysis, IR, 1HNMR, and MS measurement. The suitable reaction conditions are discussed based on the related reaction mechanism. 相似文献
66.
Norio Tsubokawa Kazuhisa Kobayashi Yasuo Sone Masato Shimomura 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1475-1486
Abstract A cation-exchange resin (a crosslinked polymer carrying carboxyl groups) was used as a model compound for carbon black, and the grafting of several polymers to the resin was investigated. Reaction of acyl chloride groups that had been placed on the ion-exchange resin with polymers having hydroxyl or amino groups, such as polypropylene glycol, polyethylene glycol, polybutadiene glycol, polyvinyl alcohol, silicone diol, silicone diamine, and polyethyleneimine, resulted in grafting to the ion-exchange resin. In further experiments, primary amino groups were placed on the cation-exchange resin by reaction of acyl chloride groups with ethylenediamine. It was found that ring-opening polymerization of γmethyl L-glutamate N-carboxyanhydride is initiated by the amino groups on the resin, and polypeptide was grafted from the cation-exchange resin. Therefore, the reactivity of carboxyl groups on the resin was found to be similar to that on carbon black. However, carboxyl groups on the resin failed to initiate the cationic polymerization of vinyl monomers, in contrast to those on carbon black. This suggested that the acidity of carboxyl groups on carbon black is greater than on the cation-exchange resin. 相似文献
67.
Vijayendra Kumar Bhavna Gupta Pramod K. Sharma Ravi Mosurkal Virinder S. Parmar Jayant Kumar 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1199-1204
The great synthetic flexibility of organosilicone polymers, their ease of processing, low cost, and nontoxic nature present an attractive alternative solution over current flame retardant materials. Novozyme-435 catalyzed amidation reaction with silicone-based oligomer was carried out to scale up the synthesis of co-polymer which was fully characterized from its detailed spectroscopic studies. Synthesized co-polymer was compounded in polyolefins for flame retardant applications. Nanoclay [Cloisite 20A, 2C18 MMT (dimethylditallowammonium-/dimethyldioctadecylammonium-modified montmorillonite)] was used as a potential additive in co-polymer, which was then blended with polyolefins to improve their thermal as well as flame retardant properties. The present work provides an initial exciting basis for the enzymatic synthesis of silicon based co-polymers in bulk and their flame retardant applications. 相似文献
68.
Decamethylcyclopentasiloxane (D5), a high production volume chemical used in personal care products, has been designated for regulation in Canada and is under review in the EU because of concerns about its persistence and potential for bioaccumulation in the environment. D5 is a volatile compound expected to be found primarily in air, but there is little information on atmospheric concentrations due to the lack of sensitive analytical methods. Here a simple and sensitive method to determine D5 in ambient air is presented. The challenge in the environmental analysis of D5 is avoiding contamination. Our method is based on the high trapping efficiency of the sorbent Isolute ENV+, combined with a comparably high sampling rate. A small amount of sorbent (10 mg) is eluted in a small volume of n-hexane (0.1–0.6 mL), which is injected onto a GC/MS system without further processing. The simplicity of the method enables the use of a field blank for every sample to trace contamination. The method provides low limits of quantification (∼0.3 ng/m3), good repeatability and limited breakthrough (∼1%). By lowering the limit of quantification compared to published work by almost two orders of magnitude, it became possible to quantify D5 in ambient air at locations remote from strong point sources. The concentrations at a rural Swedish site ranged from 0.7 to 8 ng/m3 over a period of 4 months. 相似文献
69.
Seventeen derivatives of mixed trialkyltin carboxylates with the formula (PhMe2SiCH2)Cy2SnO2CR have been synthesised.The results of IR NMR(1H,13C,119Sn) and MS showed that this kind of compounds is four-coordinated and that there are two good linear relationships between the δ 119Sn and Hammett constants of para-substitutent of the corresponding aryloxy-acetates and arylcarboxylates.These compounds have a good acaricidal activity in the preliminary bioassay tests. 相似文献
70.
设计合成了一种新型有机硅室温离子液体(SiN1IL), 并对其化学结构和电化学窗口进行表征, 通过与具有高介电常数的丙烯碳酸酯(PC)/低粘度的乙腈(AN)匹配组成电解液, 其离子电导率达到商业实际应用的要求(19.6 mS·cm-1). 对以活性炭(AC)为对称电极的超级电容器的电化学性能测试表明, SiN1IL 基电解液与活性炭有很好的界面相容性, 其高倍率充放电、阻抗性能优于商用四乙基四氟硼酸铵(Et4NBF4)/PC 电解液, 在电流密度为1000 mA·g-1的条件下, 工作电压为2.7 V, 其比电容为108 F·g-1. 相似文献