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71.
Kosuke Makiguchi Seiya Kikuchi Toshifumi Satoh Toyoji Kakuchi 《Journal of polymer science. Part A, Polymer chemistry》2013,51(11):2455-2463
The ring‐opening polymerization (ROP) of cyclic esters, such as ε‐caprolactone, 1,5‐dioxepan‐2‐one, and racemic lactide using the combination of 3‐phenyl‐1‐propanol as the initiator and triflimide (HNTf2) as the catalyst at room temperature with the [monomer]0/[initiator]0 ratio of 50/1 was investigated. The polymerizations homogeneously proceeded to afford poly(ε‐caprolactone) (PCL), poly(1,5‐dioxepan‐2‐one) (PDXO), and polylactide (PLA) with controlled molecular weights and narrow polydispersity indices. The molecular weight determined from an 1H NMR analysis (PCL, Mn,NMR = 5380; PDXO, Mn,NMR = 5820; PLA, Mn,NMR = 6490) showed good agreement with the calculated values. The 1H NMR and matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry analyses strongly indicated that the obtained compounds were the desired polyesters. The kinetic measurements confirmed the controlled/living nature for the HNTf2‐catalyzed ROP of cyclic esters. A series of functional alcohols, such as propargyl alcohol, 6‐azido‐1‐hexanol, N‐(2‐hydroxyethyl)maleimide, 5‐hexen‐1‐ol, and 2‐hydroxyethyl methacrylate, successfully produced end‐functionalized polyesters. In addition, poly(ethylene glycol)‐block‐polyester, poly(δ‐valerolactone)‐block‐poly(ε‐caprolactone), and poly(ε‐caprolactone)‐block‐polylactide were synthesized using the HNTf2‐catalyzed ROP. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 2455–2463 相似文献
72.
Itaru Natori Shizue Natori Hiroyuki Sekikawa Kosuke Tsuchiya Kenji Ogino 《Journal of polymer science. Part A, Polymer chemistry》2011,49(7):1655-1663
A poly(p‐phenylene) (PPP)‐poly(4‐diphenylaminostyrene) (PDAS) bipolar block copolymer was synthesized for the first time. A prerequisite prepolymer, poly(1,3‐cyclohexadiene) (PCHD)‐PDAS binary block copolymer, in which the PCHD block consisted solely of 1,4‐cyclohexadiene (1,4‐CHD) units, was synthesized by living anionic block copolymerization of 1,3‐cyclohexadiene and 4‐diphenylaminostyrene. To obtain the PPP‐PDAS bipolar block copolymer, the dehydrogenation of this prepolymer with quinones was examined, and tetrachloro‐1,2‐(o)‐benzoquinone was found to be an appropriate dehydrogenation reagent. This dehydrogenation reaction was remarkably accelerated by ultrasonic irradiation, effectively yielding the target PPP‐PDAS bipolar block copolymer. The hole and electron drift mobilities for PPP‐PDAS bipolar block copolymer were both on the order of 10?3 to 10?4 cm2/V·s, with a negative slope when plotted against the square root of the applied field. Therefore, this bipolar block copolymer was found to act as a bipolar semi‐conducting copolymer. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
73.
Itaru Natori Shizue Natori Anna Kanasashi Kosuke Tsuchiya Kenji Ogino 《Journal of polymer science. Part A, Polymer chemistry》2011,49(24):5322-5329
Tetraphenylporphyrin‐end‐functionalized polycyclohexane (H2TPP‐PCHE) and its metal complexes (MTPP‐PCHE) were synthesized as the first successful example of porphyrin‐end‐functionalized transparent and stable polymers with a well‐controlled and defined polymer chain structure. Chloromethyl‐end‐functionalized poly(1,3‐cyclohexadiene) (CM‐PCHD) was synthesized as prerequisite prepolymer by the postpolymerization reaction of poly(1,3‐cyclohexadienyl)lithium and chloro(chloromethyl)dimethylsilane. CM‐end‐functionalized PCHE (CM‐PCHE) was prepared by the complete hydrogenation of CM‐PCHD with p‐toluenesulfonyl hydrazide. H2TPP was incorporated onto the polymer chain end by the addition of 5‐(4‐hydroxyphenyl)‐10,15,20‐triphenylporphyrin to CM‐PCHE. The complexation of H2TPP‐PCHE and Zn(OAc)2 (or PtCl2) yielded a zinc (or platinum) complex of H2TPP‐PCHE. H2TPP‐PCHE and MTPP‐PCHE were readily soluble in common organic solvents, and PCHE did not inhibit the optical properties of the H2TPP, ZnTPP, and PtTPP end groups. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
74.
Hideko T. Oyama Yoshikazu Tanaka Sakiko Hirai Shigenari Shida Ayako Kadosaka 《Journal of Polymer Science.Polymer Physics》2011,49(5):342-354
In this study, novel biodegradable materials were successfully generated, which have excellent mechanical properties in air during usage and storage, but whose structure easily disintegrates when immersed in water. The materials were prepared by melt blending poly(L ‐lactic acid) (PLLA) and poly(butylene adipate‐co‐terephthalate) (PBAT) with a small amount of oligomeric poly(aspartic acid‐co‐lactide) (PAL) as a degradation accelerator. The degradation behavior of the blends was investigated by immersing the blend films in phosphate‐buffered saline (pH = 7.3) at 40 °C. It was shown that the PAL content and composition significantly affected morphology, mechanical properties, and hydrolysis rate of the blends. It was observed that the blends containing PAL with higher molar ratios of L ‐lactyl [LA]/[Asp] had smaller PBAT domain size, showing better mechanical properties when compared with those containing PAL with lower molar ratios of [LA]/[Asp]. The degradation rates of both PLLA and PBAT components in the ternary blends simultaneously became higher for the blends containing PAL with higher molar ratios of [LA]/[Asp]. It was confirmed that the PLLA component and its decomposed materials efficiently catalyze the hydrolytic degradation of the PBAT component, but by contrast that the PBAT component and its decomposed materials do not catalyze the hydrolytic degradation of the PLLA component in the blends. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2010 相似文献
75.
Kosuke Homma 《Journal of Number Theory》2008,128(3):500-508
In this paper we consider the distribution of fractional parts {ν/p}, where p is a prime less than or equal to x and ν is the root in Z/pZ of a quadratic polynomial with negative discriminant. This set is known to be uniformly distributed as x→∞. Here we apply the Erd?s-Turán inequality to obtain an estimate for the discrepancy. 相似文献
76.
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79.
Tsukiho Hayashi Ayumi Osawa Takehiro Watanabe Yoshiko Murata Atsushi Nakayama Kosuke Namba 《Tetrahedron letters》2017,58(20):1961-1964
1,3a,6a-Triazapentalene (TAP)-labeled enterobactin was developed as an iron ion sensor. 3-Acetylated-TAP was successfully introduced to the catechol ring of enterobactin, a well-recognized siderophore secreted by various Gram-negative bacteria. The fluorescence of TAP-labeled enterobactin decreased gradually as the amount of Fe3+ ion as an additive was increased, and 1.2 equiv of Fe3+ ion completely quenched the fluorescence. In clear contrast, when other metal ions were used, the fluorescence of TAP-labeled enterobactin remained even at 5.0 equiv. 相似文献
80.
Osuga T Murase T Ono K Yamauchi Y Fujita M 《Journal of the American Chemical Society》2010,132(44):15553-15555
Three-dimensional m × n arrays of metal ion clusters can be assembled as aromatic stacks of planar polynuclear metal complexes within columnar coordination cages. The polynuclear complexes and cage height program the final array structures of the metal ion clusters. Cyclic trinuclear Au(I) complexes (m = 3) assembled into trigonal prismatic arrays (n = 1-3) within the cages and the array structures were clearly shown by X-ray crystallographic analysis. A silver-sandwiched hetero-Au(3)-Ag-Au(3) cluster was also prepared by treating a hexanuclear Au(3)-Au(3) cluster with Ag(I) ion. 相似文献