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431.
432.
Kambe N Inoue T Takeda T Fujiwara S Sonoda N 《Journal of the American Chemical Society》2006,128(39):12650-12651
Dimetalated amides 1 (Y = O) were generated as the synthons of carbamoyllithiums 2 (Y = O) by the reaction of isocyanates with iBu2AlTenBu and a subsequent tellurium-lithium exchange reaction. A series of amide derivatives 3 (Y = O) were obtained by the trapping of dianion 1 with electrophiles. This transformation can be successfully applied to the generation and trapping of thiocarbamoyllithium synthons 1 (Y = S) as well as to the nucleophilic introduction of the parent carbamoyl moiety H2NC(O). 相似文献
433.
Satoshi Kubota Hiromasa Nishikiori Nobuaki Tanaka Morinobu Endo Tsuneo Fujii 《Journal of photochemistry and photobiology. A, Chemistry》2009,206(2-3):148-154
Pyrene crystals were grown on carbon nanofibers (CNFs) by dispersing pyrene polycrystals and CNFs in water during ultrasonic irradiation, and they were characterized by scanning electron microscopy, X-ray diffractometry (XRD) and spectroscopy. The XRD measurements indicated that the orientation and size of the pyrene crystals on the CNF aggregates were different from that of the added pyrene polycrystals. Based on the spectroscopic properties of the pyrene crystals on the CNFs, the pyrene crystals on the CNF aggregates and on the individual CNFs were determined to be polycrystals and single crystals, respectively. These results indicate that pyrene crystals are produced on the CNFs by recrystallization of the added pyrene polycrystals and their crystal states depend on the aggregation state of the CNFs. 相似文献
434.
Ninomiya K Ogino C Oshima S Sonoke S Kuroda S Shimizu N 《Ultrasonics sonochemistry》2012,19(3):607-614
Our previous study suggested new sonodynamic therapy for cancer cells based on the delivery of titanium dioxide (TiO2) nanoparticles (NPs) modified with a protein specifically recognizing target cells and subsequent generation of hydroxyl radicals from TiO2 NPs activated by external ultrasound irradiation (called TiO2/US treatment). The present study first examined the uptake behavior of TiO2 NPs modified with pre-S1/S2 (model protein-recognizing hepatocytes) by HepG2 cells for 24 h. It took 6 h for sufficient uptake of the TiO2 NPs by the cells. Next, the effect of the TiO2/US treatment on HepG2 cell growth was examined for 96 h after the 1 MHz ultrasound was irradiated (0.1 W/cm2, 30 s) to the cells which incorporated the TiO2 NPs. Apoptosis was observed at 6 h after the TiO2/US treatment. Although no apparent cell-injury was observed until 24 h after the treatment, the viable cell concentration had deteriorated to 46% of the control at 96 h. Finally, the TiO2/US treatment was applied to a mouse xenograft model. The pre-S1/S2-immobilized TiO2 (0.1 mg) was directly injected into tumors, followed by 1 MHz ultrasound irradiation at 1.0 W/cm2 for 60 s. As a result of the treatment repeated five times within 13 days, tumor growth could be hampered up to 28 days compared with the control conditions. 相似文献
435.
Poly(vinylidene fluoride) (PVDF) was incorporated in situ with silica by a sol-gel process involving tetraethoxysilane. The mechanical properties of these in situ hybrids were compared with those of PVDF composites mechanically blended with 14-nm diameter fumed silica particles. The ultimate strength of the in situ hybrids was higher than that of the blend composites, since fumed silica particles aggregate and act as mechanically weak points. The thermal analysis, dynamic viscoelastic properties, and dielectric properties were compared. The β-relaxation of PVDF caused by the glass transition was observed at around −40°C in the differential scanning calorimetry (DSC) and the mechanical tan δ curves and at −30°C in the dielectric loss factor (ϵ”) curve. The αc-relaxation due to the molecular motion in the crystalline phase occurred at 61°C in DSC curve, at 100°C in the tan δ curve, and at 80°C in the ϵ” curve. The peak positions of these relaxations did not change, but the peak intensities were decreased with the increase in silica content for both the in situ hybrids and blend composites. The activation energies for PVDF were calculated as 136 kJ/mol for the β-relaxation and 96 kJ/mol for the αc-relaxation. The result that these activation energies did not depend on silica content may indicate the weak interaction between PVDF and silica. 相似文献
436.