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11.
12.
Yasushi Mizobe Reiko Ono Yasuzo Uchida Masanobu Hidai Meguru Tezuka Suehiro Moue Atsuhiko Tsuchiya 《Journal of organometallic chemistry》1980,204(3):377-385
Diazoalkane complexes of type [MF(NNCRR′)(dpe)2][BF4] (M = Mo or W; dpe = Ph2PCH2CH2PPh2), which are easily derived from bis(dinitrogen) complexes [M(N2)2(dpe)2], undergo consecutive one- and two-electron oxidations and reductions under voltammetric conditions at a platinum electrode. The ESR spectra of the species generated by the controlled potential electrolysis show that primary oxidation occurred on the metal atom (M = Mo) and reduction on the two nitrogen atoms in the diazoalkane ligands (M = Mo or W). 相似文献
13.
Zanka A 《Chemical & pharmaceutical bulletin》2003,51(7):888-889
Primary alcohols were quantitatively oxidized in one-pot to acids via 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) mediated oxidation. The reported method is simple and suitable for large scale synthesis. 相似文献
14.
An introduction of nonlamellar-forming lipids into planar bilayers generates packing stress, which is important for the biological functions of plasma membranes and is a driving force for the lamellar-nonlamellar phase transition. We have investigated the phase behavior of a binary system consisting of egg yolk phosphatidylcholine and monoolein (MO) and the changes in the local orientation order of lipids in a lamellar-bicontinuous cubic phase transition. Small-angle X-ray scattering has revealed that the lamellar-bicontinuous cubic phase transition occurs at an MO molar fraction (X(MO)) between 0.6 and 0.7. These phases were dispersed to form liposomes and cubosomes to monitor the anisotropy of the incorporated fluorescence probe, in which Pluronic F127, used as a dispersion stabilizer of the cubic phase, has been proven not to alter the cubic structure and the location of the probes. Time-resolved fluorescence anisotropy measurements on these dispersions have revealed that the order parameter of the probe in the lamellar phase increases with increasing X(MO), and that it decreases during the transition to the cubic phase. This observation suggests that packing stress generated by the addition of the nonlamellar-forming lipid is released by the phase transition. 相似文献
15.
Tsutomu Konno Jungha Chae Tomoo Tanaka Takashi Ishihara Hiroki Yamanaka 《Journal of fluorine chemistry》2006,127(1):36-43
Hydroalumination, hydrocupration, and hydroboration reactions of various fluorine-containing alkynes were investigated. The alkyne reacted smoothly with 2.0 equiv. of Red-Al at −78 °C to give the hydroaluminated adduct in a highly regio- and stereoselective manner, which was treated with iodine, the corresponding vinyliodide being produced in moderate yield. Hydrocupration of the alkynes also took place, but the resulting vinylmetal reacted with various electrophiles sluggishly. In sharp contrast, the reaction with dicyclohexylborane proceeded smoothly to afford the cis-addition products preferentially, which were subjected to Suzuki-Miyaura cross-coupling reaction, leading to trisubstituted alkenes in high yields. 相似文献
16.
Hitoshi?MatsukiEmail author Michio?Yamanaka Hiroshi?Kamaya Shoji?Kaneshina Issaku?Ueda 《Colloid and polymer science》2005,283(5):512-520
The dissociation equilibrium between uncharged local anesthetic lidocaine (LC) and charged local anesthetic LC (LCH+) in a surface-adsorbed film was investigated by measuring the surface tension and pH of aqueous solutions of a mixture of hydrochloric acid and LC. The surface tension values decreased slightly with increasing total molality mt at 0X20.5, where X2 is the mole fraction of LC in the mixture, while they decreased rapidly with increasing mt at 0.5<X21. It was shown from the pH measurements that almost all LC molecules were changed into LCH+ ions by protonation at 0X20.5 and both forms coexisted only at 0.5<X21. The quantities of the respective LC and LCH+ transferred from the aqueous solution to the adsorbed film, i.e., their surface densities, were calculated by applying the thermodynamic equations derived to the surface tension and pH data. A greater quantity of LC than LCH+ existed in the adsorbed film at the coexisting composition. The partitioning behavior of LC and LCH+ in the adsorbed film was characterized by three composition regions: (1) slight partitioning of low surface-active LCH+ in the region at 0X20.5, (2) preferential partitioning of LC at 0.5<X2<around 0.7, and (3) negative partitioning of LCH+ at around 0.7X21. The present results clearly indicate that uncharged local anesthetics transfer into hydrophobic environments such as cell membranes more than charged ones. 相似文献
17.
Mantani T Shiomi K Konno T Ishihara T Yamanaka H 《The Journal of organic chemistry》2001,66(10):3442-3448
N,N-Dialkyl(3,3,3-trifluoro-1-propynyl)amines were readily prepared by a three-step procedure starting from commercially available 2,2,3,3,3-pentafluoropropanol. These fluorinated alkynylamines reacted smoothly with a variety of aldehydes or ketones in the presence of a catalytic amount of Lewis acid and molecular sieves 4A at ambient temperature to produce the corresponding alpha-(trifluoromethyl)-alpha,beta-unsaturated amides in good to excellent yields with high Z-stereoselectivity. 相似文献
18.
Paramagnetic centers of NH 3 + , Al, and HO2 · have been observed in alkali feldspars from Aichi prefecture, Japan. The quartet signal has been tentatively ascribed to NH 3 + rather than to ·CH3, although the hyperfine splitting by14N (I=1) was not observed. The averageg- andA-valuesg av=2.0033 andA av H =2.45 mT, respectively, were attributed to hydrogen. The powder spectra of Al centers stable up to 400 K were simulated by the anisotropicg factors ofg zz =2.060,g xx =2.0014,g yy=2.0021 andA=0.9 mT. Newly discovered HO2 · is stable up to 570 K. The intensities of the spectra from NH 3 + and Al centers were enhanced by gamma-ray irradiation, while that of HO2 · was not enhanced. Production efficiency,G-value (radical/100 eV) of NH 3 + has been obtained to beG=0.01. These results suggest that ESR dating of feldspars is possible. 相似文献
19.
Weaver M Arisaka K Roberts D Slater W Briere RA Cheu E Harris DA Roodman A Schwingenheuer B Wah YW Winstein B Winston R Barker AR Swallow EC Bock GJ Coleman R Crisler M Enagonia J Ford R Hsiung YB Jensen DA McFarland KS Ramberg E Tschirhart R Collins EM Gollin GD Nakaya T Yamanaka T Gu P Haas P Hogan WP Kim SK Matthews JN Myung SS Schnetzer S Somalwar SV Thomson GB Zou Y 《Physical review letters》1994,72(24):3758-3761
20.
Gu P Haas P Hogan WP Kim SK Matthews JN Myung SS Schnetzer S Thomson GB Zou Y Arisaka K Roberts D Slater W Spencer MB Weaver M Briere RA Cheu E Harris DA Krolak P McFarland KS Roodman A Schwingenheuer B Somalwar SV Wah YW Winstein B Winston R Barker AR Swallow EC Bock GJ Coleman R Crisler M Enagonio J Ford R Hsiung YB Jensen DA O'Dell VR Ramberg E Tschirhart R Collins EM Gollin GD Nakaya T Yamanaka T 《Physical review letters》1996,76(23):4312-4315