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Akane Suzuki Daisuke Nagai Bungo Ochiai Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2004,42(23):5983-5989
The trifunctional five‐membered cyclic carbonate 2 and dithiocarbonate 3 were successfully synthesized by the reaction of trifunctional epoxide 1 with carbon dioxide and carbon disulfide, respectively. The crosslinking reactions of 2 with p‐xylylenediamine or hexamethylenediamine were carried out in dimethyl sulfoxide at 100 °C for 48 h to produce the corresponding crosslinked poly(hydroxyurethane)s quantitatively. The crosslinking reactions of 3 with both p‐xylylenediamine and hexamethylenediamine, followed by acetylation of thiol moiety, produced the corresponding crosslinked poly(thioester–thiourethane)s quantitatively. The obtained crosslinked poly(hydroxyurethane)s were thermally more stable than the analogous crosslinked poly(thioester–thiourethane)s, probably because of less thermal stability of thiourethane moiety than hydroxyurethane moiety. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5983–5989, 2004 相似文献
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Bungo Ochiai Jun‐ichi Nakayama Masayuki Mashiko Yoshiro Kaneko Tomomi Nagasawa Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2005,43(23):5899-5905
This article describes the polyaddition of bifunctional five‐membered cyclic carbonates and diethylenetriamine. The polyaddition proceeded via the selective addition of the primary amino group to the cyclic carbonates to give poly(hydroxyurethane)s bearing a secondary amine structure in the main chain. The resulting poly (hydroxyurethane) having a secondary amine structure was crosslinked by a reaction with a bifunctional dithiocarbonate to give a networked poly(hydroxyurethane–mercaptothiourethane). © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5899–5905, 2005 相似文献
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Kazuya Uenishi Atsushi Sudo Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2005,43(19):4422-4430
A novel 5‐membered cyclic dithiocarbonate (DTC) having a siloxane moiety, 5‐(3‐trimethoxysilylpropyloxymethyl)‐1,3‐oxathiolane‐2‐thione, was synthesized from the corresponding epoxide precursor by its cycloaddition with carbon disulfide. The siloxane group underwent condensation reaction by the treatment with water and a basic or acidic catalyst, to afford the corresponding oligomer having siloxane main chain and DTC pendant. The resulting oligomer was liquid and soluble in organic solvents such as THF and chloroform. Treatment of the oligomer with amines resulted in selective ring‐opening reaction of the DTC group, generating a thiol group, which underwent oxidative coupling reaction to make the oligomer successfully cured. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4422–4430, 2005 相似文献
216.
Ki Chul Park Masatsugu Fujishige Susumu Arai Morinobu Endo 《Journal of Physics and Chemistry of Solids》2008,69(10):2481-2486
High-speed agitation by a mixing blade has efficiently achieved the cutting of a large diameter (100-150 nm) of multi-walled carbon nanotubes. The cutting process is caused by an inter-collision of the nanotubes with high transfer energy. The collision-induced cutting allows for the shortening of the nanotubes without serious damage of the original graphitic layers due to the cutting effect being limited to the collision points. Furthermore, the operation under ambient atmosphere introduces oxygen-containing functional groups to the cut nanotubes. The estimated length distribution has indicated that high-speed agitation achieves a large cutting effect during a short duration of several minutes. 相似文献
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Jun Hosoi Tetsuo Oikawa Masao Inoue Yoshio Matsui Tadashi Endo 《Journal of Electron Spectroscopy and Related Phenomena》1982,27(3):243-254
An interband π plasmon and π* edge have been observed in the spectrum of hexagonal boron nitride (h-BN). This result is in good agreement with that 相似文献