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71.
The lowest excited nπ* triplet of 9.10-anthraquinone, 1.4-naphthoquinone and 1,4-benzoquinone were studied in glassy matrices at 77 K using a time-resolved ESR method. The D value of the triplet state of 9,10-anthraquinone varied from ?0.351 cm?1 in a polar solvent to ?0.318 cm?1 in a non-polar solvent. Both 1,4-naphthoquinone and 1,4-benzoquinone in polar solvents showed triplet state spectra with a D value of ?0.330 cm?1. A computer simulation revealed the existence of widely distributed zero-field splitting parameters in the glassy condition. These data are compared with an analysis of CIDEP results of para-quinones. 相似文献
72.
73.
Yoshiyuki?KowadaEmail author Toru?Ozeki Tsutomu?Minami 《Journal of Sol-Gel Science and Technology》2005,33(2):175-185
Gel films with various pH indicators were prepared by the sol–gel method without catalysts. The obtained gel films showed good response for various pH solutions as optical pH sensors and no leaching of the indicators was observed. The feature of absorption spectra of the indicators in the gel films was almost the same as that in the aqueous solutions. pKa of the indicators in the gel films was shifted with the increase of the TMOS content in the starting solutions. These results suggest that the pH indicators in the gel films were trapped in similar environment as in the solutions. 相似文献
74.
75.
Tunable subpicosecond pulses have been obtained from a synchronously mode-locked Oxazine-1 dye laser by tandem pumping with output pulses of a mode-locked Rhodamine 6G dye laser. The effects of cavity detuning on the pulse-width and the second harmonic power (the peak intensity of the autocorrelation trace) have been investigated. The experimental results are found to be in good agreement with those predicted by a recent model analysis. 相似文献
76.
Angle-resolved photoemission measurements have been made on the metallic layer compound 2H-NbSe2. From the results, E vs k∥ dispersion curves have been obtained along two principal symmetry directions in the Brillouin zone. The experimental energy bands are found to be in good agreement with the results predicted by one-dimensional density of initial states along k⊥. 相似文献
77.
Kawasaki Y Minami T Kishimoto Y Ohno T Zenmyo K Kubo H Nakajima T Ueda Y 《Physical review letters》2006,96(3):037202
139La- and 55Mn-NMR spectra demonstrate that the ground state of the A-site-ordered perovskite manganite LaBaMn2O6 is a spatial mixture of the ferromagnetic and antiferromagnetic regions, which are assigned to the metallic and the insulating charge ordered state, respectively. This exotic coexisting state appears below 200 K via a first-order-like formation of the antiferromagnetic charge ordered state inside the ferromagnetic metal one. The Mn spin-spin relaxation rate indicates that the ferromagnetic region coexisting with the antiferromagnetic one in LaBaMn2O6 is identical to the bulk ferromagnetic metal phase of the disordered form La0.5Ba0.5MnO3 in spite of the absence of A-site disorder. This suggests a mesoscopic rather than nanoscopic nature of the ferromagnetic region in LaBaMn2O6. 相似文献
78.
Hiroshi Nagai Minami Watanabe Shingo Sato Mioko Kawaguchi Yue-Yun Xiao Kazutaka Hayashi Ryuichi Watanabe Hajime Uchida Masayuki Satake 《Tetrahedron》2019,75(17):2486-2494
The marine cyanobacterium Moorea producens is a rich source of diverse compounds that possess a variety of biological activities. In the present study, eight new aplysiatoxin derivatives, namely 6, 8–13, and 15, along with aplysiatoxin (1), debromoaplysiatoxin (2), 3-methoxyaplysiatoxin (3), anhydroaplysiatoxin (4), anhydrodebromoaplysiatoxin (5), oscillatoxin B2 (7), and 30-methyloscillatoxin D (14) were isolated and identified from the Okinawan M. producens. In cytotoxicity and diatom growth inhibition tests, the fifteen compounds tested (1–15) showed moderate or no activity at a concentration of 10?μg/mL. 相似文献
79.
Shotaro Hayashi Minami Sakamoto Fumitaka Ishiwari Takanori Fukushima Shin-ichi Yamamoto Toshio Koizumi 《Tetrahedron》2019,75(8):1079-1084
Here we report the facile derivatization of a cyano-substituted stilbene into higher π-extended analogues. The cyano-substituted stilbene, which serves as a synthetic scaffold, has a bromo group and a formyl group on its 4- and 4′-position of the phenylene rings and thus readily undergoes selective transformation into other functional groups using various simple organic reactions. The resultant π-conjugated molecules that contain a cyano-substituted stilbene skeleton exhibit fluorescence in solution and in the solid state. 相似文献
80.
Yulu Jiang Dr. Taro Ozaki Mei Harada Tadachika Miyasaka Dr. Hajime Sato Dr. Kazunori Miyamoto Dr. Junichiro Kanazawa Dr. Chengwei Liu Prof. Dr. Jun-ichi Maruyama Dr. Masaatsu Adachi Dr. Atsuo Nakazaki Prof. Dr. Toshio Nishikawa Prof. Dr. Masanobu Uchiyama Dr. Atsushi Minami Prof. Dr. Hideaki Oikawa 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(41):18152-18158
Lolitrems are tremorgenic indole diterpenes that exhibit a unique 5/6 bicyclic system of the indole moiety. Although genetic analysis has indicated that the prenyltransferase LtmE and the cytochrome P450 LtmJ are involved in the construction of this unique structure, the detailed mechanism remains to be elucidated. Herein, we report the reconstitution of the biosynthetic pathway for lolitrems employing a recently established genome-editing technique for the expression host Aspergillus oryzae. Heterologous expression and bioconversion of the various intermediates revealed that LtmJ catalyzes multistep oxidation to furnish the lolitrem core. We also isolated the key reaction intermediate with an epoxyalcohol moiety. This observation allowed us to establish the mechanism of radical-induced cyclization, which was firmly supported by density functional theory calculations and a model experiment with a synthetic analogue. 相似文献