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101.
Preparation and characterization of individual peptide-wrapped single-walled carbon nanotubes 总被引:3,自引:0,他引:3
Zorbas V Ortiz-Acevedo A Dalton AB Yoshida MM Dieckmann GR Draper RK Baughman RH Jose-Yacaman M Musselman IH 《Journal of the American Chemical Society》2004,126(23):7222-7227
Two challenges for effectively exploiting the remarkable properties of single-walled carbon nanotubes (SWNTs) are the isolation of intact individual nanotubes from the raw material and the assembly of these isolated SWNTs into useful structures. In this study, we present atomic force microscopy (AFM) evidence that we can isolate individual peptide-wrapped SWNTs, possibly connected end-to-end into long fibrillar structures, using an amphiphilic alpha-helical peptide, termed nano-1. Transmission electron microscopy (TEM) and well-resolved absorption spectral features further corroborate nano-1's ability to debundle SWNTs in aqueous solution. Peptide-assisted assembly of SWNT structures, specifically in the form of Y-, X-, and intraloop junctions, was observed in the AFM and TEM images. 相似文献
102.
Shuichi Hirata Kouichi Tanaka Katsuya Matsui Fernando Arteaga Arteaga Yasushi Yoshida Shinobu Takizawa Hiroaki Sasai 《Tetrahedron: Asymmetry》2013,24(19):1189-1192
The introduction of a 1,3-propanediamine unit at the 3-position of (S)-BINOL using a methylene spacer led to the formation of a chiral bifunctional organocatalyst for the aza-Morita–Baylis–Hillman (aza-MBH) reaction. The organocatalyst 1k mediated aza-MBH transformations with high chemical yields and with up to 82% ee. 相似文献
103.
S. Nezu S. Walsh V. Meille M. Yoshida J. B. Lando 《Journal of polymer science. Part A, Polymer chemistry》1995,33(6):973-977
The dimer, trimer, and tetramer of 1,11-dodecadiyne, HC?C? (CH2)8? C?CH, were synthesized. The solid-state polymerization of the dimer was investigated by infrared (IR) spectroscopy. IR bands due to the diacetylene moiety were identified through the comparison of the IR spectra of the dimer, trimer, and tetramer. The dimer was found to have two polymorphs, melt-crystallized and solution-crystallized. Both of the polymorphs undergo solid-state polymerization by exposure to γ-ray or UV irradiation. The former has higher polymerizability for the diacetylene moiety than the latter. The solid-state polymerization of the terminal acetylene group was not observed. It is shown that the previously reported dimer structure in which both the diacetylene and terminal acetylene groups are polymerized to form an inherently electrically conducting polymer is incorrect. © 1995 John Wiley & Sons, Inc. 相似文献
104.
Kunihisa Yoshida Yoshimasa Toyo-Oka Kazusada Takeda 《Journal of heterocyclic chemistry》1995,32(2):701-702
The electrooxidation of 1-methylpyrazole in methanol containing sodium cyanide produced 1-methyl-pyrazole-4-carbonitrile 2 and ?5-carbonitrile 3 in yields of 23 and 8%, respectively (2e-oxidation products), together with 4-methoxy-1-methylpyrazole-5-carbonitrile 4 (4e-oxidation product, 4%). 相似文献
105.
Dr. Emi Uchida Dr. Kouji Sakaki Dr. Yumiko Nakamura Dr. Reiko Azumi Dr. Yuki Hirai Dr. Haruhisa Akiyama Dr. Masaru Yoshida Dr. Yasuo Norikane 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(51):17391-17397
Photoinduced phase transitions caused by photochromic reactions bring about a change in the state of matter at constant temperature. Herein, we report the photoinduced phase transitions of crystals of a photoresponsive macrocyclic compound bearing two azobenzene groups ( 1 ) at room temperature on irradiation with UV (365 nm) and visible (436 nm) light. The trans/trans isomer undergoes photoinduced phase transitions (crystal–isotropic phase–crystal) on UV light irradiation. The photochemically generated crystal exhibited reversible phase transitions between the crystal and the mesophase on UV and visible light irradiation. The molecular order of the randomly oriented crystals could be increased by irradiating with linearly polarized visible light, and the value of the order parameter was determined to be ?0.84. Heating enhances the thermal cis‐to‐trans isomerization and subsequent cooling returned crystals of the trans/trans isomer. 相似文献
106.
Tetsushi Kijima Masakazu Nishida Haruhiko Fukaya Masato Yoshida Hideo Sawada 《Journal of polymer science. Part A, Polymer chemistry》2013,51(12):2555-2564
A reddish‐brown fluoroalkyl end‐capped 2‐acrylamido‐2‐methylpropanesulfonic acid (AMPS) oligomer/acetone composite was prepared by heating the white oligomer powder with acetone at 80 °C for 3 h. The color was not observed in the corresponding non‐fluorinated AMPS oligomer/acetone composite, which was prepared under similar conditions. The coloring was probably caused by the formation of acetone polyaldol condensation products in the fluorinated oligomeric gel network cores. The colored RF‐(AMPS)n‐RF/acetone composite powders were stable and did not exhibit any color change after 2 years in natural light at room temperature. The colored composite powders dissolved in methanol to give a reddish‐brown solution at room temperature. However, the retro‐polyaldol condensation decolored the solution after 1 day at room temperature. This is the first example of the retro‐aldol polycondensation of acetone under mild conditions. The decoloration increased by between 38‐ and 70‐fold under UV irradiation, compared with that in dark conditions. The coloring–decoloring behavior was consistent and repeatable; therefore our fluorinated oligomer/acetone composites are promising candidates for new fluorinated coloring materials. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 2555–2564 相似文献
107.
In order to assess the levels and behavior of129I (half-life: 1.6×107 y) and127I (stable) in the environment, we have developed analytical procedures involving neutron activation analysis (NAA). Environmental samples collected around Tokaimura, Ibaraki Prefecture, Japan, have been analyzed using this method. Ranges of129I and127I concentrations in surface soil were 0.9–180 mBq kg–1 and 1–60 mg kg–1, respectively. Higher129I concentrations were found in soil samples collected from coniferous forests, suggesting a contribution from tree canopies in the deposition of this nuclide. Most of the129I in soil, was found to be retained in the first 10 cm. The129I/127I ratios in wheat fields were lower than those in rice paddy fields.A soil sample collected by IAEA from an area contaminated by the Chemobyl accident was also determined. The129I concentration and the129I/127I ratio were 1.6 mBq kg–1 and 1.7×10–7, respectively. The129I level in this sample was higher than the values obtained in areas far from nuclear facilities in Japan. It was suggested that the analysis of129I in soils in the Chernobyl area may be useful in evaluating the131I levels at the time of the accident.Analyses of129I and127I by ICP-MS in water samples were also made. The analytical speed of this method was very high, i.e., 3 minutes for a sample. However, there is a sensitivity limitation for129I detection due to interference from129Xe with the129I peak. The detection limits for129I and127I in water samples were about 0.5 mBq ml–1 and 0.1 ng ml–1, respectively. 相似文献
108.
Transport phenomenon of three sulfonated azo dyes, C.I. Acid Red 88, C.I. Direct Yellow 12, and C.I. Direct Blue 15 into water-swollen cellulose membranes has been analyzed on the basis of parallel transport theory by surface and pore diffusion. Langmuir equation was applied into the mass balance equation to estimate dye concentration in the pores. The results were compared with the results obtained by applying Freundlich equation in our previous papers. The surface diffusivity (D
s) and the pore diffusivity (D
p) for the parallel diffusion model obtained by applying Langmuir equation agreed with those obtained by applying Freudlich equation. The theoretical concentration profiles for parallel diffusion calculated usingD
s andD
p coincided accurately with the experimental data when we applied either Langmuir or Freundlich equations. 相似文献
109.
110.
Yoshitomo Kashiwagi Yumiko Takamori Kentaro Yoshida Tetsuya Ono 《Electroanalysis》2013,25(12):2575-2577
This paper describes the electrocatalytic oxidation of amines on TEMPO (2,2,6,6‐tetramethylpiperidine‐1‐oxyl)‐modified electrodes prepared by electrochemical copolymerization of TEMPO precursor containing pyrrole side chain and 2,2′‐bithiophene. The modified electrode exhibits electrocatalytic activity for the oxidation of primary and secondary amines. Cyclic voltammetric studies showed that the peak current of the cyclic voltammogram increased linearly with increasing concentration of amine in the sample solution. 相似文献