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141.
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Tsuneyuki Sato Masahiko Hashimoto Makiko Seno Tomohiro Hirano 《Journal of polymer science. Part A, Polymer chemistry》2003,41(12):1819-1830
The polymerizations of α‐ethyl β‐N‐(α′‐methylbenzyl)itaconamates carrying (RS)‐ and (S)‐α‐methylbenzylaminocarbonyl groups (RS‐EMBI and S‐EMBI) with dimethyl 2,2′‐azobisisobutyrate (MAIB) were studied in methanol (MeOH) and in benzene kinetically and with electron spin resonance (ESR) spectroscopy. The initial polymerization rate (Rp) at 60 °C was given by Rp = k[MAIB]0.58 ± 0.05[RS‐EMBI]2.4 ± 0.l and Rp = k[MAIB]0.61 ± 0.05[S‐EMBI]2.3 ± 0.l in MeOH and Rp = k[MAIB]0.54 ± 0.05[RS‐EMBI]1.7 ± 0.l in benzene. The rate constants of initiation (kdf), propagation (kp), and termination (kt) as elementary reactions were estimated by ESR, where kd is the rate constant of MAIB decomposition and f is the initiator efficiency. The kp values of RS‐EMBI (0.50–1.27 L/mol s) and S‐EMBI (0.42–1.32 L/mol s) in MeOH increased with increasing monomer concentrations, whereas the kt values (0.20?7.78 × 105 L/mol s for RS‐EMBI and 0.18?6.27 × 105 L/mol s for S‐EMBI) decreased with increasing monomer concentrations. Such relations of Rp with kp and kt were responsible for the unusually high dependence of Rp on the monomer concentration. The activation energies of the elementary reactions were also determined from the values of kdf, kp, and kt at different temperatures. Rp and kp of RS‐EMBI and S‐EMBI in benzene were considerably higher than those in MeOH. Rp of RS‐EMBI was somewhat higher than that of S‐EMBI in both MeOH and benzene. Such effects of the kinds of solvents and monomers on Rp were explicable in terms of the different monomer associations, as analyzed by 1H NMR. The copolymerization of RS‐EMBI with styrene was examined at 60 °C in benzene. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1819–1830, 2003 相似文献
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[Structure: see text] A Pd/C-catalyzed chemoselective hydrogenation using diphenylsulfide as a catalyst poison has been developed. This methodology selectively hydrogenates olefin and acetylene functionalities without hydrogenolysis of aromatic carbonyls and halogens, benzyl esters, and N-Cbz protective groups. 相似文献
147.
Tomohiro Sato Katsuyoshi Ito Tsutomu Tamada Akihiko Kanki Shigeru Watanabe Hirotake Nishimura Daigo Tanimoto Hiroki Higashi Akira Yamamoto 《Magnetic resonance imaging》2013,31(8):1412-1417
ObjectivesTo quantify tissue gadolinium (Gd) deposition in renally impaired rats exposed to Gd-EOB-DTPA and other Gd-based MRI contrast agents by means of inductively coupled plasma mass spectrometry (ICP-MS), and to compare the differences in distribution among major organs as possible triggers for nephrogenic systemic fibrosis (NSF).MethodsA total of 15 renally impaired rats were injected with Gd-EOB-DTPA, Gd-DTPA-BMA and Gd-HP-DO3A. Gd contents of skin, liver, kidney, lung, heart, spleen, diaphragm and femoral muscle were measured by inductively coupled plasma mass spectrometry (ICP-MS). Histological assessment was also conducted.ResultsTissue Gd deposition in all organs was significantly higher (P = 0.005 ~ 0.009) in the Gd-DTPA-BMA group than in the Gd-HP-DO3A and Gd-EOB-DTPA groups. In the Gd-DTPA-BMA group, Gd was predominantly deposited in kidney (1306 ± 605.7 μg/g), followed by skin, liver, lung, spleen, femoral muscle, diaphragm and heart. Comparing Gd-HP-DO3A and Gd-EOB-DTPA groups, Gd depositions in the kidney, liver and lung were significantly lower (P = 0.009 ~ 0.011) in the Gd-EOB-DTPA group than in the Gd-HP-DO3A group although no significant differences were seen for any other organs.ConclusionsGd-EOB-DTPA is a stable and safe Gd-based contrast agent (GBCA) showing lower Gd deposition in major organs in renally impaired rats, compared with other GBCAs. This fact suggests that the risk of NSF onset would be low in the use of Gd-EOB-DTPA. 相似文献
148.
The effect of magnetic fields on out-of-plane orientations of liquid crystalline polymers (LCPs) under simple shear flows is numerically analyzed using the Doi–Hess equation. The evolution equation for the probability distribution function of the LCP molecules is directly solved without any approximation closure. The initial director is parallel to the vorticity direction. Two cases of the magnetic fields are considered (1) the magnetic field parallel to the flow direction, and (2) the magnetic field parallel to the velocity gradient direction. For both cases a log-rolling orientation state is detected at low shear rates. However, the director is quickly aligned along the direction of magnetic fields because of the deformation of molecules. The field affects on the scalar order parameter rather than the major orientation direction for the magnetic field parallel to the flow direction. On the other hand regarding the magnetic field along the vorticity gradient direction, the effect of the magnetic field is more remarkable on the major orientation in comparison with the effect on the scalar order parameter. Also it is be found that the order parameter is increased obviously with increasing the magnetic fields. It is an efficient way to improve the performance of LCP materials. 相似文献
149.
Tomohiro Itagaki 《代数通讯》2013,41(8):3472-3497
In this article, we compute the Hochschild homology group of A = KΓ/(f(X s )), where KΓ is the path algebra of the cyclic quiver Γ with s vertices and s arrows over a commutative ring K, f(x) is a monic polynomial over K, and X is the sum of all arrows in KΓ. Moreover, we compute the cyclic homology group of A in the case f(x) = (x ? a) m , where a ∈ K, so that we can determine the cyclic homology of A in general when K is an algebraically closed field. 相似文献
150.
Tomohiro Umeno Atsushi Ueda Mitsunobu Doi Takuma Kato Makoto Oba Masakazu Tanaka 《Tetrahedron letters》2019,60(49):151301
The introduction of a five-membered ring α,α-disubstituted α-amino acid into l-Leu-based heptapeptides preferentially induced right-handed (P) helical structures. Using 5 ~ 20 mol% of a single helical foldamers-catalyst, enantioselective 1,4-addition reactions of dialkyl malonates to cycloalk-2-enones (5 ~ 7 rings) proceeded to give chiral 3-substituted cycloalkanones with 94 ~ 99% ee in moderate chemical yields, regardless of the ring size of substrates. 相似文献