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排序方式: 共有1177条查询结果,搜索用时 46 毫秒
41.
Takahito Itoh Hiroki Saitoh Shouji Iwatsuki 《Journal of polymer science. Part A, Polymer chemistry》1995,33(10):1589-1596
1,1′-Dialkylferrocene-3,3′-dicarbaldehydes ( 1a–c ) with long alkyl chains such as ethyl, hexyl, and dodecyl groups were prepared in 13–25% yield via three-step reactions. The titanium-induced dicarbonyl-coupling reaction of 1a–c gave poly(1,1′-dialkyl-3,3′-ferrocenylenevi-nylene)s ( 2a–c ) in quantitative yields, which were the molecular weights of 3000–10,000 and highly soluble in chloroform, benzene, and hexane. The electrical conductivity and the third-order nonlinear optical susceptibility for poly(1,1′-dihexyl-3,3′-ferrocenylenevinylene) ( 2b ) were estimated to be 1 × 10?2 S/cm on doping with iodine and 1–4 × 10?12 esu at a wavelength of 1–2.4 μm, respectively. © 1995 John Wiley & Sons, Inc. 相似文献
42.
Oku K Watanabe H Kubota M Fukuda S Kurimoto M Tsujisaka Y Komori M Inoue Y Sakurai M 《Journal of the American Chemical Society》2003,125(42):12739-12748
Trehalose is a disaccharide that attracts much attention as a stress protectant. In this study, we investigated the mechanism of the antioxidant function of trehalose. The spin-lattice relaxation times (T(1)) of (1)H and (13)C NMR spectra were measured to investigate the interaction between trehalose and unsaturated fatty acid (UFA). We selected several kinds of UFA that differ in the number of double bonds and in their configurations (cis or trans). Several other disaccharides (sucrose, maltose, neotrehalose, maltitol, and sorbitol) were also analyzed by NMR. The T(1) values for the (1)H and (13)C signals assigned to the olefin double bonds in UFA decrease with increasing concentration of trehalose and the changes reaches plateaus at integer ratios of trehalose to UFA. The characteristic T(1) change is observed only for the combination of trehalose and UFA with cis double bond(s). On the other hand, from the (13)C-T(1) measurements for trehalose, the T(1) values of the C-3 (C-3') and C-6' (C-6) are found to change remarkably by addition of UFA. (1)H[bond](1)H NOESY measurements provide direct evidence for complexation of trehalose with linoleic acid. These results indicate that one trehalose molecule stoichiometrically interacts with one cis-olefin double bond of UFA. Computer modeling study indicates that trehalose forms a stable complex with an olefin double bond through OH...pi and CH...O types of hydrogen bonding. Furthermore, a significant increase in the activation energy is found for hydrogen abstraction reaction from the methylene group located between the double bonds that are both interacting with the trehalose molecules. Therefore, trehalose has a significant depression effect on the oxidation of UFA through the weak interaction with the double bond(s). This is the first study to elucidate the antioxidant function of trehalose. 相似文献
43.
Iwao Hashimoto Takatoshi Kawaji Florin D. Badea Tsuyoshi Sawada Shuntaro Mataka Masashi Tashiro Gouki Fukata 《Research on Chemical Intermediates》1996,22(9):855-869
The Friedel-Crafts acylations of various aromatic compounds with cyclic anhydrides such as 2-(p-substituted phenyl)butanedioic, 3-phenylpentanedioic and homophathlic anhydrides were carried out under various conditions in order to obtain informations about the regioselectivity of the ring opening of the cyclic anhydrides and about the possible reaction pathways in the acylations. 相似文献
44.
The stereoselective total synthesis of (+)-(Z)-laureatin is described. The 3,8-dioxabicyclo[5.1.1]nonane skeleton possessing trans-orientated alkyl substituents at the α,α′-positions to the ether linkage was stereoselectively constructed via formation of the oxetane arising from 4-exo cyclization of hydroxy epoxide existing on the oxocene core. 相似文献
45.
Wataru Sugimoto Masashi Omoto Katsunori Yokoshima Yasushi Murakami Yoshio Takasu 《Journal of solid state chemistry》2004,177(12):4542-4545
An ion-exchangeable ruthenate with a layered structure, K0.2RuO2.1, was prepared by solid-state reactions. The interlayer cation was exchanged with H+, C2H5NH3+, and ((C4H9)4N+) through proton-exchange, ion-exchange, and guest-exchange reactions. The electrical and magnetic properties of the products were characterized by DC resistivity and susceptibility measurements. Layered K0.2RuO2.1 exhibited metallic conduction between 300 and 13 K. The products exhibited similar magnetic behavior despite the differences in the type of interlayer cation, suggesting that the ruthenate sheet in the protonated form and the intercalation compounds possesses metallic nature. 相似文献
46.
R.V. Denys V.A. Yartys Masashi Sato R.G. Delaplane 《Journal of solid state chemistry》2007,180(9):2566-2576
A new intermetallic deuteride Ce2Ni7D4.7 with an anomalous volume expansion has been studied. Its structure was solved on the basis of in situ neutron diffraction data. Expansion proceeds along the c-axis and within the CeNi2 slabs only. All D atoms are located inside these slabs and on the border between CeNi2 and CeNi5. Ordering of D atoms in the bulk of CeNi2 is accompanied by substantial deformation of these slabs thus lowering the hexagonal symmetry to orthorhombic [space group Pmcn (No. 62); a=4.9251(3) Å, b=8.4933(4) Å, c=29.773(1) Å]. Inside the CeNi2 layer the hydrogen sublattice is completely ordered; all D-D distances exceed 2.0 Å. Local coordination of Ni by D inside the CeNi2 blocks is of “open”, saddle-like type. Hydrogen ordering is mainly determined by Ce-H and H-H interactions. The pressure-composition-temperature measurements yielded the following thermodynamic parameters of the formation of the hydride: ΔH=−22.4 kJ/molH, ΔS=−59.9 J/(K molH). 相似文献
47.
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49.
Abstract The reaction of aluminum alkoxide in straight-chain primary alcohols at elevated temperatures yielded the alkyl derivatives of boehmite [AlO(OH)1-x (OR) x ], a class of intercalation compound where the guest moieties are covalently bonded to the host boehmite layers. The addition of small amounts of water to the reaction system yielded another phase having a larger basal spacing. XRD, IR, and elemental analysis showed that the products had the boehmite layer structure with the alkyl moieties incorporated between the boehmite layers. IR spectra of the products also exhibited bands due to hydrogen bonding between the boehmite layers. These results suggest that the products are the alkyl derivatives of boehmite having the second stage structure. Because water in the reaction medium facilitated the hydrolysis of intermediate aluminum alkoxides, the product with the second stage structure had smaller alkyl/Al ratio and therefore had smaller basal spacing than that expected from the corresponding first stage product. 相似文献
50.
Tetsuo Kusumoto Ken-Ichi Sato Kumiko Ogino Tamejiro Hiyama Sadao Takehara Masashi Osawa 《Liquid crystals》2013,40(3):727-732
Abstract New chiral dopants β-hydroxy ketones 1, 1,3-diols 2, 1,3-dioxanes 3 and 1,3-dioxan-2-ones 4 were designed and synthesized. Reaction of (R)-1,2-epoxyoctane with carbanions derived from 2-(4-substituted phenyl)-1,3-dithianes followed by hydrolysis of the resulting hydroxy dithianes afforded 1. Reduction of 1 gave the diols 2, which yielded 3 upon acetalization and 4 upon carbonation. The syn isomers of 2, 3, and 4 exhibited larger spontaneous polarizations, when applied as chiral dopants, than the anti isomers or hydroxy ketones 1. 相似文献