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71.
[reaction: see text] Smooth and selective Payne rearrangement was achieved for the above types of epoxyalcohols with a CF(3) group so as to form thermodynamically more stable alkoxides, where the strongly electron-withdrawing nature of this moiety played a significantly important role and was proved to overcome increased steric instability of epoxides from syn-E to anti-Z isomers. 相似文献
72.
[structure: see text] Synthesis and fluorescence properties of pi-conjugated compounds having alternately an aromatic ring such as benzene, pyridine, and thiophene and an enediyne unit in the backbone are described. 相似文献
73.
Ultraviolet second-harmonic generation in first-order periodically poled MgO:LiNbO3 is presented. Using a high-voltage multipulse application method, we fabricated a first-order nonlinear grating with a period of 1.8 microm and depth of approximately 150 microm over 10-mm interaction length in a 1-mm-thick MgO:LiNbO3 substrate. In a single-pass configuration, continuous-wave 30-mW UV light at 362.5 nm was generated for a fundamental power of 522 mW, corresponding to a normalized conversion efficiency of 11%/W. 相似文献
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Nam‐Ho You Tomoya Higashihara Shinji Ando Mitsuru Ueda 《Journal of polymer science. Part A, Polymer chemistry》2010,48(12):2604-2609
New sulfur‐containing polymers with high‐refractive indices and low birefringences have been developed as UV‐curable high‐refractive polymer resins. The polymers derived from 2,7‐bis[(2‐acryloylethyl)sulfanyl]thianthrene (2,7‐BAST) and 4,4′‐bis[(acryloyloxyethylthio)diphenylsulfide (4,4′‐BADS) were prepared by photopolymerization under UV irradiation. Transparent UV‐cured films were obtained in both cases. Both polymers showed good thermal stability, such as a 5% weight‐loss temperature at 355 °C under nitrogen and glass transition temperatures (Tg) in the range of 94–143 °C. They also showed high‐refractive indices of 1.6531 and 1.6645 at 632.8 nm and low birefringences of 0.0039 and 0.0069 in addition to high transparency in the visible region. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2604–2609, 2010 相似文献
77.
Tomohito Ogura Tomoya Higashihara Mitsuru Ueda 《Journal of polymer science. Part A, Polymer chemistry》2009,47(13):3362-3369
A positive‐type photosensitive polyimide (PSPI) based on poly(amic acid) (PAA), a crosslinker 1,1,1‐tris{4‐[2‐(vinyloxy)ethoxy]phenyl}ethane (TVPE), a photoacid generator (PAG) (5‐propylsulfonyloxyimino‐5H‐thiophen‐2‐ylidene)‐2‐(methylphenyl)acetonitrile (PTMA), and a thermobase generator (TBG) t‐butyl 2,6‐dimethylpiperidine‐1‐carboxylate (BDPC) has been developed as a promising material in microelectronics. The PAA was prepared from 3,3′,4,4′‐biphenyltetracarboxylic dianhydride (BPDA) and 4,4′‐oxydianiline (ODA) in dimethyl sulfoxide (DMSO). The PSPI, consisting of PAA (69 wt %), TPVE (21 wt %), PTMA (3 wt %), and BDPC (7 wt %), showed high sensitivity of 21 mJ/cm2 and a high contrast of 6.8 when it was exposed to a 436‐nm line (g‐line), postbaked at 90 °C for 5 min, and developed with 1.69 wt % TMAHaq. A clear positive image of 8 μm line and space pattern was printed on film, which was exposed to 50 mJ/cm2 of g‐line by a contact printing mode and fully converted to the corresponding polyimide (PI) pattern on heating at 200 °C, confirmed by FTIR spectroscopy. Thus, this system will be a good candidate for next generation PSPIs. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3362–3369, 2009 相似文献
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Optical Review - In this study, the effects of selectively yellow-cut lenses on contrast sensitivity were investigated in healthy young and middle-aged individuals and elderly patients with... 相似文献
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Yasuko Ishizuka Hiroshi Nakanishi Takanori Shiraishi Yasuo Kogure Shoichi Kobayashi 《Journal of carbohydrate chemistry》2013,32(4):583-592
ABSTRACT 1H NMR spectra of some oligosaccharide substituted cyclodextrins composed of only α-D-glucose units are analysed. Chemical shifts of protons of each glucosyl group of the chain were determined by experiments with the HOHAHA pulse technique. In spite of the similar kinds of protons, dispersion of chemical shifts is observed. The most dispersed proton is the anomeric proton, and the largest change in the chemical shifts is 0.5 ppm. 相似文献