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81.
Masakazu Yoshikawa Katsunori Koso Kyoichi Yonetani Satoshi Kitamura Satoshi Kimura 《Journal of polymer science. Part A, Polymer chemistry》2005,43(2):385-396
Molecularly imprinted polymeric membranes were prepared from various oligopeptide tweezers by the adoption of N‐α‐tert‐butoxycarbonyl‐D ‐tryptophan (Boc‐D ‐Trp) or N‐α‐tert‐butoxycarbonyl‐L ‐tryptophan (Boc‐L ‐Trp) as a print molecule. The chiral recognition ability of the formed molecular recognition sites was dependent on the absolute configuration of the print molecule adopted in the membrane preparation (molecular imprinting) process, whereas the candidate oligopeptide tweezers consisted of the L ‐amino acid residues. In other words, the membranes imprinted by the D ‐isomer recognized the D ‐isomer in preference to the corresponding L ‐isomer, and vice versa. The affinity constant between the target molecule and the chiral recognition site from the oligopeptide tweezers was higher than that from a single‐strand oligopeptide derivative. Those membranes selectively transported the enantiomer, which was preferentially incorporated into the membrane by dialysis. The permselectivities for these membranes exceeded their adsorption selectivities. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 385–396, 2005 相似文献
82.
Katsunori Watabe Hisashi Kanda Katsuya Sato Toshiyuki Hobo 《Journal of chromatography. A》1992,590(2):289-296
In continuous counter-current gas-liquid chromatography, which has a high resolving power and is suitable for the large-scale purification of organic solvents, it is very important that the samples that can be applied extend from easily separable to more difficult to separate, such as azeotropes, low-volatility compounds and stereoisomers. A system was designed and constructed for high-temperature operation up to 200°C, and was applied to the separation of dimethyl and diethyl phthalate, trans- and cis-decahydronaphthalene and cis-decahydronaphthalene and tetrahydronaphthalene. It was confirmed that over 99% of purity could be achieved for dimethyl and diethyl phthalate, trans-decahydronaphthalene, and tetrahydronaphthalene. 相似文献
83.
84.
Carbazole Dendrimers as Solution‐Processable Thermally Activated Delayed‐Fluorescence Materials
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Assist. Prof. Ken Albrecht Assist. Prof. Kenichi Matsuoka Assoc. Prof. Katsuhiko Fujita Prof. Kimihisa Yamamoto 《Angewandte Chemie (International ed. in English)》2015,54(19):5677-5682
Recently, thermally activated delayed fluorescence (TADF) materials have received increasing attention as effective emitters for organic light‐emitting diodes (OLEDs). However, most of them are usually employed as dopants in a host material. In this report, carbazole dendrimers with a triphenyl‐s‐triazine core are reported, which are the first solution‐processable, non‐doped, high‐molecular‐weight TADF materials. The dendrimers were obtained by a new and facile synthetic route using the tert‐butyldimethylsilyl moiety as a protecting group. All dendrimers showed TADF in toluene. Measurements of the temperature‐dependent luminescence lifetime revealed that spin‐coated neat films also showed TADF with moderate quantum yields. OLED devices incorporating these dendrimers as spin‐coated emitting layers gave external quantum efficiencies of up to a 3.4 %, which suggests that this device is harvesting triplet excitons. This result indicates that carbazole dendrimers with attached acceptors are potential TADF materials owing to their polarized electronic structure (with HOMO–LUMO separation). 相似文献
85.
We consider parabolic operators of fractional order and their iterates on the upper half space of the euclidean space. We deal with Hilbert spaces of solutions of those parabolic equations. We shall show, in this note, the existence of reproducing kernels and give a formula by using their fundamental solutions. As an application, we also discuss the polyharmonic Bergman spaces and give their reproducing kernels by using the Poisson kernel on the upper half space. 相似文献
86.
Ghosh A Yusa S Matsuoka H Saruwatari Y 《Langmuir : the ACS journal of surfaces and colloids》2011,27(15):9237-9244
Cationic amphiphilic diblock copolymers of poly(n-butylacrylate)-b-poly(3-(methacryloylamino)propyl)trimethylammonium chloride) (PBA-b-PMAPTAC) with various hydrophobic and hydrophilic chain lengths were synthesized by a reversible addition-fragmentation chain transfer (RAFT) process. Their molecular characteristics such as surface activity/nonactivity were investigated by surface tension measurements and foam formation observation. Their micelle formation behavior and micelle structure were investigated by fluorescence probe technique, static and dynamic light scattering (SLS and DLS), etc., as a function of hydrophilic and hydrophobic chain lengths. The block copolymers were found to be non-surface active because the surface tension of the aqueous solutions did not change with increasing polymer concentration. Critical micelle concentration (cmc) of the polymers could be determined by fluorescence and SLS measurements, which means that these polymers form micelles in bulk solution, although they were non-surface active. Above the cmc, the large blue shift of the emission maximum of N-phenyl-1-naphthylamine (NPN) probe and the low micropolarity value of the pyrene probe in polymer solution indicate the core of the micelle is nonpolar in nature. Also, the high value of the relative intensity of the NPN probe and the fluorescence anisotropy of the 1,6-diphenyl-1,3,5-hexatriene (DPH) probe indicated that the core of the micelle is highly viscous in nature. DLS was used to measure the average hydrodynamic radii and size distribution of the copolymer micelles. The copolymer with the longest PBA block had the poorest water solubility and consequently formed micelles with larger size while having a lower cmc. The "non-surface activity" was confirmed for cationic amphiphilic diblock copolymers in addition to anionic ones studied previously, indicating the universality of non-surface activity nature. 相似文献
87.
Saya Nakabayashi Katsunori Nagano Makoto Nakamura Junya Togawa Asami Kurokawa 《Adsorption》2011,17(4):675-686
The aim of this study is the development of a new adsorbent for the desiccant material which can be regenerated by the domestic
exhaust heat by using natural mesoporous material, Wakkanai siliceous shale. To improve this shale’s performance to adsorb/desorb
the water vapor, lithium chloride, calcium chloride or sodium chloride was supported into the mesopores by impregnating with
each chloride solution. Especially sodium chloride was effective to increase the water vapor adsorption amount 5–7 times of
that of natural shale in the relative humidity range from 50 to 70%. Moreover, the appropriate impregnating concentrations
were determined as 5wt% from the relationship between the maximum water vapor adsorption amount and the mesopore volume. Based
on these results, a new desiccant filter has been developed by impregnated original paper with lithium chloride and sodium
chloride. This paper contained shale powder in the synthetic fibers. The dehumidification performance of this filter was evaluated
under the simulated summer condition in Tokyo. From the cyclic adsorption/regeneration test, this shale and chlorides filter
could adsorb and desorb 60 g/h water vapor repeatedly at the regeneration temperature of 40°C. On the other hand, a silica
gel filter and a zeolite filter adsorbed and desorbed only 10 g/h and 25 g/h, respectively. These results suggested that the
shale impregnated with the chlorides has the best dehumidification ability as a new desiccant material. Further, the desiccant
filter made from the shale will achieve the effective use of the low temperature exhaust heat. 相似文献
88.
89.
Matsuoka H Shen JR Kawamori A Nishiyama K Ohba Y Yamauchi S 《Journal of the American Chemical Society》2011,133(12):4655-4660
The oxidation of a redox-active tyrosine residue Y(Z) in photosystem II (PSII) is coupled with proton transfer to a hydrogen-bonded D1-His190 residue. Because of the apparent proximity of Y(Z) to the water-oxidizing complex and its redox activity, it is believed that Y(Z) plays a significant role in water oxidation in PSII. We investigated the g-anisotropy of the tyrosine radical Y(Z)(?) to provide insight into the mechanism of Y(Z)(?) proton-coupled electron transfer in Mn-depleted PSII. The anisotropy was highly resolved by electron paramagnetic resonance spectroscopy at the W-band (94.9 GHz) using PSII single crystals. The g(X)-component along the phenolic C-O bond of Y(Z)(?) was calculated by density functional theory (DFT). It was concluded from the highly resolved g-anisotropy that Y(Z) loses a phenol proton to D1-His190 upon tyrosine oxidation, and D1-His190 redonates the same proton back to Y(Z)(?) upon reduction. 相似文献
90.