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41.
Enami S Yamanaka T Hashimoto S Kawasaki M Tonokura K 《The journal of physical chemistry. A》2005,109(27):6066-6070
The reactions of Cl atoms with RI (R = n-C3H7, n-C4H9, cyclo-C6H11, C6H5, C6F5, and p-CH3C6H4) have been studied using cavity ring-down spectroscopy at a temperature range of 233-313 K and at 100 Torr total pressure of N2 diluent. Visible absorption spectra of the RI-Cl adducts were recorded at 440-520 nm at 263 K. The yields of the adducts were temperature-dependent. There was no discernible reaction of the adducts in the presence of 100 Torr of O2 at 263 K. Theoretical calculations were performed for C4H9I-Cl and C6H5I-Cl for quantitative explanation of the absorption spectra and the strength of the I-Cl bonds in the charge-transfer complexes. Evidence for the adduct formation following the reaction of Cl with C6H5Br was sought but not found at 440 and 520 nm. 相似文献
42.
Yoshimasa Hama Kazuya Hosono Yasuro Furui Kenichi Shinohara 《Journal of polymer science. Part A, Polymer chemistry》1971,9(5):1411-1419
ESR studies of ultraviolet-irradiated polyethylene (PE) were carried out. Irradiation effects different from those of high-energy radiation are observed. Ultraviolet radiation is absorbed selectively, and especially in carbonyl groups in PE produced by oxidation. Radicals produced were identified as \documentclass{article}\pagestyle{empty}\begin{document}$ \hbox{---} {\rm CH}_2 \hbox{---} {\dot {\rm C}} {\rm H} \hbox{---}{\rm CHO}$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ \hbox{---} {\rm CH}_2 \hbox{---} {\dot {\rm C}} {\rm H} \hbox{---}{\rm CH}_2 \hbox{---}$\end{document}. Some radicals giving a quintet signal stable at room temperature were also observed but remained unidentified. The radical \documentclass{article}\pagestyle{empty}\begin{document}$ \hbox{---} {\rm CH}_2 \hbox{---} {\dot {\rm C}} {\rm H} \hbox{---}{\rm CHO}$\end{document} undergoes a mutual conversion with the acyl radical: 相似文献
43.
T Abe K Horiuchi H Kikuchi T Aritsuka Y Takata E Fukushi Y Fukushi J Kawabata K Ueno S Onodera N Shiomi 《Chemistry Central journal》2012,6(1):89
ABSTRACT: BACKGROUND: Sugar beet molasses is a viscous by-product of the processing of sugar beets into sugar. The molasses is known to contain sucrose and raffinose, a typical trisaccharide, with a well-established structure. Although sugar beet molasses contains various other oligosaccharides as well, the structures of those oligosaccharides have not been examined in detail. The purpose of this study was isolation and structural confirmation of these other oligosaccharides found in sugar beet molasses. RESULTS: Four oligosaccharides were newly isolated from sugar beet molasses using high-performance liquid chromatography (HPLC) and carbon-Celite column chromatography. Structural confirmation of the saccharides was provided by methylation analysis, matrix-assisted laser desorption/ionaization time of flight mass spectrometry (MALDI-TOF-MS), and nuclear magnetic resonance (NMR) measurements. CONCLUSION: The following oligosaccharides were identified in sugar beet molasses: beta-D-galactopyranosyl-(1- > 6)-beta-D-fructofuranosyl-(2 <-> 1)-alpha-D-glucopyranoside (named beta-planteose), alpha-D-galactopyranosyl-(1- > 1)-beta-D-fructofuranosyl-(2 <-> 1)-alpha-D-glucopyranoside (named1-planteose), alpha-D-glucopyranosyl-(1- > 6)-alpha-D-glucopyranosyl-(1 <-> 2)-beta-D-fructofuranoside (theanderose), and beta-D-glucopyranosyl-(1- > 3)-alpha-D-glucopyranosyl-(1 <-> 2)-beta-D-fructofuranoside (laminaribiofructose). 1-planteose and laminaribiofructose were isolated from natural sources for the first time. 相似文献
44.
Rumiko Sakurai Kenichi Sakai Koichi Kodama Masanori Yamaura 《Tetrahedron: Asymmetry》2012,23(3-4):221-224
A useful key intermediate for the dipeptidyl peptidase-4 (DPP-4) inhibitor, 3-aminopiperidine 1, was successfully resolved with an enantiomerically pure resolving agent, N-tosyl-(S)-phenylalanine 2, to give both stereoisomers (R)-1 and (S)-1 as a less-soluble diastereomeric salt with (S)-2, via a dielectrically controlled resolution (DCR) phenomenon. 相似文献
45.
Tabito Ikezaki Reishi Matsuoka Kenichi Hatanaka Naoko Yoshie 《Journal of polymer science. Part A, Polymer chemistry》2014,52(2):216-222
We synthesized biobased poly(2,5‐furandimethylene succinate‐co‐butylene succinate) [P(FS‐co‐BS)] copolymers by polycondensation of 2,5‐bis(hydroxymethyl)furan, 1,4‐butanediol, and succinic acid. These copolymers could be crosslinked to form network polymers by means of a reversible Diels–Alder reaction with bis‐maleimide. The thermal properties, mechanical properties, and healing abilities of the P(FS‐co‐BS)s and the network polymers were investigated. The mechanical properties of the network polymers depended on the comonomer composition of the P(FS‐co‐BS)s and the maleimide/furan ratio in the network polymers. Some of the copolymers exhibited healing ability at room temperature, and their healing efficiency was enhanced by solvent or heat. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 216–222 相似文献
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48.
Reaction of FeCl3 with poly(N-methyl-2,5-pyrrolylene) (PNMPy), poly(2,5-thienylene) (PTh), and poly(3-methyl-2,5-thienylene) (P3MeTh) caused reduction of FeCl3 to afford Fe2+ species. Variable temperature Mössbauer spectra of the reaction systems indicated formation of FeCl2 and FeCl? 4. The latter is regarded as a counter-anion for the cation delocalized along the π-conjugated polymer chain. 相似文献
49.
Condensation reaction of 3,5-di-O-benzoyl-1,2-O-(1-cyanoben-zylidene)-β-D-arabinofuranose (2) with benzyl and allyl 2,3-di-O-benzoyl-5-O-triphenylmethyl-α-L-arabinofuranosides (5a and 5b) in methylene chloride in the presence of triphenylcarbenium tetrafluoroborate as catalyst under high vacuum gave α-(1→5)-linked dimeric D-arabinofuranoside derivatives (6a and 6b). One of the dimeric compounds (6a) was debenzoylated, triphenylmethylated, and rebenzoylated to give a dimeric homolog of 5a (8). Similarly for the preparation of 6a, 8 was condensed with 2 to provide an α-(1→5)-linked trimeric D-arabinofuranoside derivative (9). Further elongation of the glycoside chain might be possible in the same way. 相似文献
50.
Kenichi Takeo Kimiko Nagayoshi Kenichi Nishimura Shinichi Kitamura 《Journal of carbohydrate chemistry》2013,32(8):1159-1177
Abstract The 8-methoxycarbonyloctyl β-glycosides of the trisaccharides O-β-d-Glcp-(1 → 6)- O-β-d-Glcp-(1 → 3)-d-Glcp and O-β-d-Glcp-(1 → 3)-O-[β-d -Glcp-(1 → 6)]-d-Glcp and of the tetrasaccharide O-β-d-Glcp-(1 → 3)-O-[β-d-Glcp-(1 → 6)]-O-β-d-Glcp-(1 → 3)-d-Glcp, corresponding to the fragments of schizophyllan, have been synthesized by using mono- to tetrasaccharide 1-thioglycosides as glycosyl donors, each bearing a participating benzoyl group in the 2-position, and N-iodosuccinimide and silver triflate as promoter. Saponification of the tri- and tetrasaccharide β-glycosides, followed by attachment to bovine serum albumin of the resulting sugar derivatives having a carboxyl group at the aglycon terminal, provided neoglycoproteins for immunological studies of the polysaccharide. 相似文献