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1.
Satoshi Ito Kazuya Koizumi Katsuhiko Fukuda Naohiro Kameta Tsukasa Ikeda Toru Oba Kazuhisa Hiratani 《Tetrahedron letters》2006,47(48):8563-8566
A new series of BINOL-based macrocycles with two phenolic protons have been synthesized via oxidative coupling reaction using CuCl(OH)-TMEDA. 相似文献
2.
Kazuhisha Hiratani Shamsun Naher Michinori Karikomi Kazuo Haga 《Journal of heterocyclic chemistry》2005,42(4):575-582
Novel crownophanes with 27‐ and 28‐membered rings having two hydroxyl groups, two amide groups, and aromatic moieties such as naphthalene, pyridine, and phenyl rings were successfully synthesized by a one‐step reaction from the corresponding macrocyclic polyethers via “tandem Claisen rearrengement” in moderate yields. They can solubilize urea and its derivatives into chloroform solution, while the corresponding macrocyclic polyethers do not solubilize them. According to NMR studies, crownophanes 1 and 2 interact with urea and its derivatives forming 1:1 complexes. 相似文献
3.
The reaction of titanium isopropoxide with a Schiff base ligand containing an isobutenyl linker leads to double stranded dinuclear titanium(IV)-Schiff base complexes through self-assembly with concomitant formation of intramolecular mu-oxo bridges upon hydrolysis. 相似文献
4.
Houjou H Kanesato M Hiratani K Mandon D 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(18):4576-4583
Novel diiron complexes with an Fe2(mu-OMe)2 core were studied as models of the active site of nonheme iron-containing enzymes. X-ray crystal structures of the complexes showed the existence of two types of ligand folding-parallel and twisted-both of which have four virtually equivalent phenolato groups sticking out from the Fe2O2 rhombic plane. Cyclic voltammetry measurements revealed two or more distinct redox waves in a region of relatively high potential, in addition to known Fe(II)/Fe(III) redox waves in a region of lower potential. These new peaks were assigned to the high-valence state of iron atoms, that is, Fe(III)Fe(IV) and Fe(IV)Fe(IV), resonating with the phenoxyl radical(s). The split width of the redox waves ranged from 0.14 to 0.20 eV, which may be a measure of the electronic interaction of the phenolate groups through the Fe2(mu-OMe)2 core. 相似文献
5.
Kazuhisa Hiratani Isao Nozawa Tsutomu Nakagawa Sumio Yamada 《Journal of membrane science》1982,12(2):207-215
The effects of acid and cation concentration on the uphill transport rates of cations and selectivities through chloroform liquid membrane by noncyclic polyether ionophores, which are pentaethylene glycol derivatives containing both 8-quinolyt and o-carboxylphenyl terminal groups, have been demonstrated. Using sulfuric, oxalic, or polyphosphoric acid in aqueous solution, the initial transport rates and the amount of cation transported by the ionophores after two days were larger than those using hydrochloric or nitric acid. Using picric acid, the amount of cation transported decreased greatly. It was confirmed that it decreased where an acid could easily be counter-transported by the ionophore through liquid membranes. On the other hand, it was found that the rates, amounts of cation transported, and selectivities, change with the changing of the cation concentration in the aqueous solutions. When the cation concentration in both aqueous solutions is high enough compared with the pH gradient between the two aqueous solutions, the rate, amount, and selectivity of the ionophore for potassium ion increases compared with when the cation concentration is low. 相似文献
6.
Charge transport properties of β-LiAl were studied in the composition range of 48.0–50.2 at.% Li. Measurements were made on single crystal samples and down to the liquid He temperature. The resistivity changes linearly with temperature above 125 K, with a thermal coefficient of 72–95nΩ cm K?1. The Matthiessen law was obeyed very well. A component dependent on temperature, which was described by the Grüneisen formula, is insensitive to a change of the chemical composition. On the other hand, the residual resistivity depends largely on the composition and contributes up to 58% of the total resistivity in Li0.498. It is chiefly due to the substituted Li atoms on the Al sublattice. 相似文献
7.
Jie Hao Kazuhisa Hiratani Naohiro Kameta Toru Oba 《Journal of inclusion phenomena and macrocyclic chemistry》2009,65(3-4):257-262
A novel tripodand having 3-hydroxy-2-naphthoeic amide groups was prepared by the reaction of 1,3,5-tris(aminomethyl)-2,4,6-trimethylbenzene with 3-allyloxy-2-naphthoeic acid chloride followed by thermal Claisen rearrangement. This tripodand can exhibit the anion binding ability in chloroform solution. In particular, it can bind with acetate, dihydrogen phosphate, and fluoride ions to form 1:1 complexes. 相似文献
8.
Amidecrownophane-type macrocycles with different number of hydroxy groups were prepared in quantitative yields by control of the conditions of thermal reaction with the aim to examine the role of hydroxy groups in anion recognition. It was proved that the hydroxy group played a critical role in anion binding for this type of macrocycles and the anion binding affinity could be tuned by different number of hydroxy groups. Further exploration clarified the presence of intramolecular hydrogen-bonding and exhibited the major effect on their anion binding potential. 相似文献
9.
Crown ether-type macrocycles consisting of an enantiopure biarenol derivative and an oligoethylene glycol were synthesized by the Lewis acid-mediated tandem Claisen rearrangement. This is the first example of the successful application of the tandem Claisen rearrangement to the synthesis of enantiopure macrocyclic biarenol derivatives. The enantiopure macrocyclic biarenols were found to form 1:1 complexes with amino acid salts and to discriminate their chirality. 相似文献
10.
Michinori Karikomi Mari Yamada Hirohiko Houjou Kazuhisa Hiratani Tadao Uyehara 《Tetrahedron letters》2005,46(35):5867-5869
Oxidative coupling reaction of both 3-hydroxychrysene and 2-hydroxybenzo[c]phenanthrene by using Cu(NO3)2-3H2O under atmospheric air is described. The former gave the aimed coupled biaryl derivative. However, the latter gave a further oxidized helical quinone derivative. The unique helical structure was characterized by X-ray and NMR analysis. 相似文献