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961.
Takahashi K Kawakami T Gu ZZ Einaga Y Fujishima A Sato O 《Chemical communications (Cambridge, England)》2003,(18):2374-2375
The first preparation of an Fe(II) spin-crossover complex including a 1,3-dithiole ligand is reported. Crystal analyses of both the low- and the high-temperature phases reveal that short S...S contacts play a key role in an abrupt spin transition. 相似文献
962.
Yamayoshi A Iwase R Yamaoka T Murakami A 《Chemical communications (Cambridge, England)》2003,(12):1370-1371
Hairpin type psoralen-cojugated oligonucleotides cross-linked with RNA when they hybridized with a perfectly complementary RNA. 相似文献
963.
Kirishima A Kimura T Tochiyama O Yoshida Z 《Chemical communications (Cambridge, England)》2003,(7):910-911
The luminescence spectrum of U4+ in aqueous solution was observed in the UV-Vis region with the lifetime < 20 ns at room temperature by excitation light corresponding to the 5f-5f electronic transition. All the luminescence peaks were assigned to individual electronic transitions. 相似文献
964.
Asano A Sullivan CM Yanagisawa A Kimoto H Kurotsu T 《Analytical and bioanalytical chemistry》2002,374(7-8):1250-1255
Interactions between poly alpha- L-glutamic acid (PGA) and metal ions Cd(2+), Co(2+) were studied by direct current polarography. The diffusion currents of these ions decreased sharply in the presence of PGA in the pH region from 5.0 through neutral. A corresponding increase in the helix content of the PGA-metal ion complex was revealed by CD measurements on the same solutions. Helix contents determined by polarography were in good agreement with those by CD in the neutral pH region. On the contrary, the decrease of current in lower acidic pH regions was independent of helix formation and suggested that metal ions coordinate to sporadically-dissociated carboxylate groups to cause aggregation of the intra and/or inter polymer chains. The diffusion current of the ions, therefore, is a parameter sensitive to the conformational changes of PGA from acidic through neutral pH region. 相似文献
965.
Irreducibility of W1
d (X) for d g - (k - 2) [(h + 3)/2] - h+ 1, where X is a curve of genus g which admits an odd prime degree k map onto a general curve C of genus h > 0 is proved. Also, the existence of a component of W1
d(X) with expected dimension on a general k-sheeted covering X over a curve C is shown. 相似文献
966.
Let be a distance-regular graph of diameterd, valencyk andr=max{i|(c
i
,b
i
)=(c
1,b
1)}. In this paper, we prove that
相似文献
967.
Ryosuke Kadono Akira Matsushita Kusuo Nishiyama Kanetada Nagamine 《Hyperfine Interactions》1994,87(1):979-984
In order to shed new light on the initial loss of muon spin polarization, or socalled missing fraction, which is commonly observed in non-metallic solids, we have studied muon-induced excitation in various alkali halides by measuring the luminescences associated with the radiative decay of the self-trapped excitons (STE). The result strongly suggests that the spin-exchange interaction between muonium and muon radiolysis products including STE's causes fast muon depolarization in those materials. 相似文献
968.
Jiro Motoyoshiya Akira Takagi Kiyoichi Hirakawa Toshio Kakurai 《Journal of heterocyclic chemistry》1986,23(2):597-599
Several ketenimines bearing ester groups were prepared and their thermal reactions gave 2-alkoxy-3-substituted-4-quinolinols VIa-e via presumed iminoketene intermediates. Subsequent oxidation of 2-alkoxy-3-(3-methylbut-2-enyl)-4-quinolinols VIc and VId provided pyranoquinolines VIIIa and VIIIb. 相似文献
969.
Jyunichi Koyanagi Katsumi Yamamoto Kouji Nakayama Akira Tanaka 《Journal of heterocyclic chemistry》1994,31(4):1093-1095
4-endo-5-exo-Dibromo-3-methyl-3,6-endo-oxyperhydrophthalic anhydride 3b and 4-exo-5-endo-dibro-mo-3-methyl-3,6-endo-oxyperhydrophtbalic anhydride 3c were isolated from the bromo-adducts of 3-methyl-3,6-endo-oxy-1,2,3,6-tetrahydrophthalic anhydride 2. When 3b or 3c was heated in quinoline, only 3-bromo-2-methylfuran 4 was obtained from 3b and only 4-bromo-2-methylfuran 5 from 3c. 相似文献
970.
The reaction of phenyl or 1-alkenyl iodides with 1-alkenyl-1,3,2-benzodioxaboroles readily obtainable via the hydroboration of 1-alkynes, gives the corresponding “head-to-tail” cross-coupling products, 2-phenyl-1-alkenes or 2-alkyl-1,3-alkadienes, in good yields. The reaction is effectively catalyzed by catalytic amounts of palladium compounds in the presence of triethylamine. 相似文献