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91.
Tatsuro Ouchi Hiroshi Sakamoto Yoshifumi Hosaka Minoru Imoto Tsutomu Iwamoto 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(8):1025-1038
Abstract The polymerization of some kinds of vinyl monomer was found to occur without an ordinary initiator in aqueous solutions of AB-type block or random copolymers of sodium methacrylate with styrene as a so-called “uncatalyzed polymerization.” Although the spin trapping technique showed that the initiation mechanism by the block copolymer was the same as that by the random copolymer, the initiating ability of the block copolymer was lower than that of the random copolymer. Such results are attributable to the difference in the incorporating ability of monomer into the micelles formed by the block copolymer and into the hydrophobic areas formed by the random copolymer. 相似文献
92.
Copolymerization of an optically active N-(1-menthyl carboxylatomethyl)citraconimide (MCMCI) was carried out with methyl methacrylate (MMA) with azobisisobutyronitrile as the initiator in benzene at 50°C. All the copolymers obtained were optically active. After the removal of the optically active menthyl group, the hydrolyzed poly(MCMCI-co-MMA)'s still showed optical activity. The asymmetric induction to the copolymer main chain and the mechanism are discussed based on the measurements of optical rotatory dispersion and circular dichroism of the original and hydrolyzed copolymers. 相似文献
93.
Tatsuro Ouchi Kazuo Hagita Hiroshi Sakamoto Minoru Imoto Tsutomu Iwamoto 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1651-1665
Abstract The polymerization of some kinds of vinyl monomer was found to occur in aqueous solutions of poly(ethylene glycol) diglycolic acid (PEG Acid) or sodium poly(ethylene glycol) diglycolate (PEG Acid Na) through radical mechanisms without any further initiator, as a so-called “uncatalyzed polymerization.” Although the initiating radical species for PEG Acid was determined to be the same as that for PEG Acid Na by means of the spin-trapping technique, the initiating ability of PEG Acid was higher than that of PEG Acid Na. These results are assumed to be attributable to the difference in the initiation mechanisms of the two systems and in the incorporating abilities of monomer into the hydrophobic areas formed by PEG Acid and PEG Acid Na. 相似文献
94.
Atsunori Morigaki Kazuki Tsukade Satoru Arimitsu Tsutomu Konno Toshio Kubota 《Tetrahedron》2013,69(5):1521-1525
The reaction of β-fluoroalkylated α,β-unsaturated ketones with various enamines gave 4-fluoroalkylated 3,4-dihydro-2H-pyrans as a major product in good yields by a one-pot operation, and these products display the high diastereoselection just after single recrystallization. This unexpected result is rationalized by the unique reactivity of β-fluoroalkylated α,β-unsaturated ketones. As the synthetic application, 4-trifluoromethyl tetrahydropyran was synthesized in moderate isolated yield with high diastereoselectivity. 相似文献
95.
In this paper, we report the preparation and red-light-emitting behavior of benzothiadiazole–tris(alkyloxy)phenylethene dyes. In solution, we observed an efficient red light emission with high fluorescence quantum yields (up to 0.78). With increase in solvent polarity, the emission bands shifted to longer wavelengths accompanied by a large Stokes shift of up to 152 nm. A moderate fluorescence quantum yield of 0.52 could be achieved even in the polar solvent dimethylformamide. Red light emission with good fluorescence quantum yields (up to 0.50) was also observed in the bulk solid, liquid, and film state. 相似文献
96.
Little is known of the biosynthesis of sesquarterpenes and the synthesis of unnatural terpenoids by sesquarterpene biosynthetic enzymes has not yet been reported. In this study, the enzymatic cyclization of head-to-tail acyclic triterpene β-hexaprene—a natural product isolated from Bacillus clausii—using tetraprenyl-β-curcumene cyclase (TC) from Bacillus subtilis resulted in the formation of two unnatural pentacyclic triterpenes. It was revealed that B. subtilis TC, which forms tetracyclic terpenoid scaffold from tetraprenyl-β-curcumene in vivo, could be used to construct the 6/6/6/6/6-fused pentacyclic scaffold in vitro, suggesting that the active site cavity of TC has sufficient space to accommodate this unnatural pentacyclic scaffold. This is the first report demonstrating the utility of a sesquarterpene cyclase toward the synthesis of unnatural terpenoids. 相似文献
97.
98.
Masami Sakamoto Kazuya Yoshiwara Fumitoshi Yagishita Wataru Yoshida Takashi Mino Tsutomu Fujita 《Research on Chemical Intermediates》2013,39(1):385-395
The irradiation of methyl 2- and 3-chromonecarboxylate in the presence of various alkenes afforded cyclobutane type adducts, whose structures were established by X-ray structural analysis. Methyl 2-chromonecarboxylate showed higher photochemical reactivity than methyl 3-chromonecarboxylate, in which endo adducts were yielded as major products. 相似文献
99.
Prof. Dr. Tsutomu Ishi-i Honoka Tanaka Rihoko Kichise Christopher Davin Takaaki Matsuda Dr. Naoya Aizawa Dr. In Seob Park Prof. Dr. Takuma Yasuda Taisuke Matsumoto 《化学:亚洲杂志》2021,16(15):2136-2145
The regulation of multicolor fluorescence changes in mechanochromic fluorescence (MCF) remains a challenging task. Herein, we report the regulation of MCF using a donor-acceptor structure. Two crystal polymorphs, BTD-pCHO(O) and BTD-pCHO(R) produced by the introduction of formyl groups to an MCF dye, respond to a mechanical stimulus, allowing a three-color fluorescence change. Specifically, the orange-colored fluorescence of the metastable BTD-pCHO(O) polymorph changed to a deep-red color in the amorphous-like state to finally give a red color in the stable BTD-pCHO(R) polymorph. This change occurred by mechanical grinding followed by vapor fuming. The two different crystal packing patterns were selectively regulated by the electronic effect of the introduced functional groups. The two types of selectively formed crystals in BTD(F)-pCHO bearing fluorine atoms, and BTD(OMe)-pCHO bearing methoxy groups, respond to mechanical grinding, allowing for the regulation of multicolor MCL from a three-color change to two different types of two-color changes. 相似文献
100.
Yoshiki K Kanamaru R Ryosuke K Hashimoto M Hashimoto N Araki T 《Optics letters》2007,32(12):1680-1682
We developed a compact polarization-mode converter for microscopy to control three-dimensional polarization at the focus. The converter consisted of two homogeneously aligned liquid-crystal spatial light modulators with eight independently controllable electrodes (segments), and a quarter-waveplate. The converter converted a linearly polarized beam to three polarization modes: two orthogonal linear polarizations and a pseudo-radial polarization. We applied the converter to second-harmonic-generation microscopy and demonstrated the detection of three-dimensional molecular orientation. 相似文献