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71.
Kensuke Naka Adriana Gelover‐Santiago Takashi Uemura Yoshiki Chujo 《Journal of polymer science. Part A, Polymer chemistry》2003,41(5):708-715
Dithiafulvene oligomers ( 3 ) were prepared by cycloaddition polymerization of aldothioketenes with their alkynethiol tautomers derived from 1,4‐diethynylbenzene ( 2 ) with the addition of 1‐ethynyl‐4‐methylbenzene ( 1 ) as a monofunctionalized compound. Different feed ratios of 2 / 1 were used to control the molecular weights of 3 . The structures of 3 were confirmed by IR and 1H NMR spectroscopies in comparison with those of 2‐(4‐tolylidene)‐4‐tolyl‐1,3‐dithiol ( 4 ) as a model compound, which was obtained by the treatment of lithium 2‐tolylethynethiolate with water in Et2O. The number‐average degree of polymerization (DP) and the number‐average molecular weight were measured by gel permeation chromatographic and 1H NMR analysis. DP increased with an increasing feed ratio of 2 / 1 . The ultraviolet–visible spectra of 3 in diluted acetonitrile showed that the absorption maxima of 3 increased with an increasing DP of 3 . These redshifts are ascribed to an effective expansion of the π‐conjugation system in 3 . The oligomers exhibited a maximum conjugation length of seven repeating units. The redox properties of 3 were examined by cyclic voltammetry. The oxidation half‐peak potentials (Ep/2) of 3 were slightly cathodically shifted with increasing DP. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 708–715, 2003 相似文献
72.
73.
Daisuke Uemura Katsuhiro Ueda Yoshimasa Hirata Hideo Naoki Takashi Iwashita 《Tetrahedron letters》1981,22(29):2781-2784
The full structure of palytoxin, a potent coelenterate toxin, is reported. 相似文献
74.
Akio Toshimitsu Toshiaki Aoai Hiroto Owada Sakae Uemura Masaya Okano 《Tetrahedron》1985,41(22):5301-5306
The reaction of phenylselenenyl chloride with olefins in aqueous acetonitrile affords β-hydroxyalkyl phenyl selenides in excellent yields, providing the most convenient method for hydroxyselenation of olefins so far reported. When the reaction was applied to conjugated dienes, monohydroxyselenated products were obtained in good to excellent yields. From non-conjugated dienes, on the other hand, cyclic ethers containing two phenylseleno groups were produced in good to excellent yields, the first step of this reaction being the hydroxyselenation of one double bond. 相似文献
75.
76.
77.
Yasutomo J. Uemura 《Hyperfine Interactions》1981,8(4-6):739-748
78.
Oxidation of several linear conjugated dienes with tellurium (IV) oxide and lithium bromide in acetic acid affords an isomeric mixture of the corresponding diacetoxyalkenes (1,2- and 1,4-addition products), 1,4-isomer being highly selectively produced when the ratio of LiBr/TeO2, is 5–10. 相似文献
79.
Y.J. Uemura R.S. Hayano J. Imazato N. Nishida T. Yamazaki 《Solid State Communications》1979,31(10):731-734
The zero-field spin relaxation function of μ+ observed in ZrH2 has revealed that the second moment of the nuclear dipolar broadening is five times larger than the high-field value. This experiment clearly demonstrates the recovery of the non-secular part of dipolar interaction between unlike spins. A general expression of zero-field relaxation function is presented to account for a slow modulation of random fields on μ+ found at room temperature. 相似文献
80.
The addition of arylboronic acids 1 to azodicarboxylates 2 in the presence of a catalytic amount of a copper salt under mild reaction conditions gives aryl-substituted hydrazines 3 in high yields. The reaction is tolerant of a wide variety of functional groups. 相似文献