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21.
Terai T Araho D Osakabe K Katai M Narama I Matsuura T Katakawa J Tetsumi T Sato M 《Chemical & pharmaceutical bulletin》2000,48(1):142-144
The structure of iso-grayanotoxin II, a new diterpenoid from Leucothoe grayana MAX., has been determined as 3 beta,5 beta,6 beta,14 beta,16 alpha-pentahydroxygrayanotox-9(10)-ene by spectroscopic and X-ray crystallographic analysis. The lethal dosage level of iso-grayanotoxin II in mice was lower than that of grayanotoxin III. 相似文献
22.
Cao B Hasegawa M Okada K Tomiyama T Okazaki T Suenaga K Shinohara H 《Journal of the American Chemical Society》2001,123(39):9679-9680
23.
24.
Tsugikazu Tomono Etsuo Hasegawa Eishun Tsuchida 《Journal of polymer science. Part A, Polymer chemistry》1974,12(5):953-965
Active hydrogen compounds such as hydroquinone (HQ), cyclohexanone (CH), acetophenone (AP), and 4,4′-methylene bis-N-methylaniline (MNA) polymerized with formaldehyde (F) and secondary diamines to produce Mannich base polyamine polymers. The HQ-containing polymers were oxidized to benzoquinone (BQ)-containing polymers and their redox properties were investigated in the desulfurization of hydrogen sulfide. 相似文献
25.
Akio Nara Nobuko Kobayashi Kazuko Hasegawa Katsuko Honba Shigeo Baba 《Microchemical Journal》1975,20(4):440-448
For the conductometric titration of fluoride with calcium acetate, solvent system in sample solution and titrant, concentration, and acidity of sample solution were examined to establish the titration conditions. Results of these examinations were transferred to the microdetermination of fluorine in organic compounds using oxygen flask combustion method.Comparative examination between quartz and Pyrex flasks for the combustion of fluorine samples indicated that good results were obtained by the use of the former flask, whereas the use of the latter one gave negative values of 1.0–1.6% due to the formation of boron fluoride during the combustion. 相似文献
26.
Hasegawa JY Takata K Miyahara T Neya S Frisch MJ Nakatsuji H 《The journal of physical chemistry. A》2005,109(14):3187-3200
Excited states of free-base porphyrin isomers, porphycene (Pc), corrphycene (Cor), and hemiporphycene (hPc), were studied by the Symmetry-Adapted Cluster (SAC)/SAC-Configuration Interaction (CI) method. The absorption peaks of the porphyrin isomers were assigned on the basis of the SAC-CI spectra. The X, Y, X', and Y' bands of the porphyrin isomers, which have weak intensities, are identified. The differences in the Q-band absorptions among the isomers were clearly explained by the four-orbital model. In Cor and hPc, the wave function of the B-band corresponds to the mixture of the four-orbital excitations and the optically forbidden excitation of free-base porphin (P), due to the molecular symmetry lowering in the isomers. The B-band character is described by the five-orbital model in Pc and the six-orbital model in Cor and hPc. Two tetrazaporphycenes and two ring-extended (dibenzo) porphycenes were designed, and the Q-band transition moment was successfully controlled. These examples show that the control of the four-orbital energy levels is the guiding principle for pigment design in porphyrin compounds. 相似文献
27.
28.
Masaki Hasegawa Kazuhiko Saigo Hirokazu Katsuki Noriyuki Yonezawa Toshio Kanoe 《Journal of polymer science. Part A, Polymer chemistry》1983,21(8):2345-2362
The ring-opening polyaddition reaction of anti and syn head-to-head Coumarin dimers with diamines and the photocleavage behavior of the resulting polyamides were investigated. Anti head-to-head Coumarin dimer successfully reacted with aliphatic and aromatic diamines in an aprotic polar solvent to give corresponding high molecular weight polyamides. The polyamides showed good film forming ability and exhibited solubility behavior typical of polyelectrolytes. Furthermore, these polyamides were found to undergo exclusively asymmetric photocleavage on the cyclobutane rings in the polymer main chain to give a fumaramide unit with elimination of 2,2′-dihydroxystilbene. On the other hand, syn head-to-head Coumarin dimer gave only low molecular weight polyamides. These polymerization and photocleavage behaviors were elucidated in comparison with those of model reactions. 相似文献
29.
Hasegawa E Takizawa S Iwaya K Kurokawa M Chiba N Yamamichi K 《Chemical communications (Cambridge, England)》2002,(17):1966-1967
Photoinduced electron transfer reaction of 2-bromomethyl-2-(3-butenyl)benzocyclic-1-alkanones with amines afforded 5-exo radical cyclization products while electron transfer reaction with samarium diiodide produced cyclopropanols. 相似文献
30.
T. Kambara K. Hasegawa H. Yoshioka Y. Kamiya T. Kotani K. Tabei 《Journal of Radioanalytical and Nuclear Chemistry》1977,36(1):87-94
Variations of125Sb valency states in HCl solutions were investigated by the use of the N-benzoyl-N-phenyl-hydroxylamine (BPHA) extraction
method.125Sb(V) is completely reduced to Sb(III) by one hour refluxing in conc. HCl.125Sb(III) is gradually oxidized to Sb(V) in solutions of low HCl concentrations by the effects of their own radiations. Natural
light promotes such oxidation reactions. By utilizing such oxidation-reduction effects125Sb(V) can be easily prepared from125Sb(III) and also125Sb(III) can be prepared by the reduction of Cl
aq
−
. Their valency states were stable on keeping them in brown-colored bottles at 6M HCl concentrations. 相似文献