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951.
Kuse N Nomura Y Ozawa A Kuwata-Gonokami M Watanabe S Kobayashi Y 《Optics letters》2010,35(23):3868-3870
Compensation of the intracavity dispersion in the mode-locked oscillator is known to be one of the most important factors for ultrashort pulse generation. However, recent investigations of a Yb-doped fiber mode-locked oscillator revealed that precise third-order dispersion (TOD) compensation is not always necessary for ultrashort pulse generation, owing to the strong nonlinearity that compensates residual TOD without reducing its spectral bandwidth. The origin of the nonlinear TOD compensation has remained unclear. To investigate the process in detail, we studied the pulse evolution inside a 30 fs Yb-doped fiber mode-locked oscillator both experimentally and numerically, and we found that the nonlinear phase shift with a temporally asymmetric pulse shape introduces an appropriate amount of TOD that exactly cancels the residual cavity dispersion. 相似文献
952.
Tomoya Higashihara Kenji Sugiyama Hee‐Soo Yoo Mayumi Hayashi Akira Hirao 《Macromolecular rapid communications》2010,31(12):1031-1059
This paper reviews the precise synthesis of many‐armed and multi‐compositional star‐branched polymers, exact graft (co)polymers, and structurally well‐defined dendrimer‐like star‐branched polymers, which are synthetically difficult, by a commonly‐featured iterative methodology combining living anionic polymerization with branched reactions to design branched polymers. The methodology basically involves only two synthetic steps; (a) preparation of a polymeric building block corresponding to each branched polymer and (b) connection of the resulting building unit to another unit. The synthetic steps were repeated in a stepwise fashion several times to successively synthesize a series of well‐defined target branched polymers.
953.
Hiroaki Kitagishi Dr. Yasuaki Kakikura Hiroyasu Yamaguchi Dr. Koji Oohora Akira Harada Prof. Dr. Takashi Hayashi Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(7):1271-1274
Supramolecular protein polymers : When a heme moiety was introduced to the surface of an apo‐cytochrome b562(H63C) mutant, supramolecular polymers formed through noncovalent heme–heme pocket interactions. The incorporation of a heme triad as a pivot molecule in the protein polymer further led to a two‐dimensional protein network structure, which was visualized by tapping‐mode atomic force microscopy (see picture).
954.
Tolis EI Engelhardt LP Mason PV Rajaraman G Kindo K Luban M Matsuo A Nojiri H Raftery J Schröder C Timco GA Tuna F Wernsdorfer W Winpenny RE 《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(35):8961-8968
The synthesis and structural characterization of a nonanuclear FeIII cage complex is reported. The nine iron centers in [Fe9(mu3-O)4(O3PPh)3(O2CCMe3)13] lie on the vertices of an incomplete icosahedron, with the P atoms of triphenylphosphonate at the other three vertices. The paramagnetic core therefore describes a tridiminished icosahedron. Magnetic studies suggest an S=1/2 ground state for the molecule. Analysis of exchange paths and the susceptibility data point to the interpretation that the cluster can be divided into two nearly decoupled sections: an {Fe6O3} section, with an S=0 ground state, in which three oxo-centered triangles bound a central triangle that is not oxo-centered; and an {Fe3O} triangle with S=1/2. The analysis of the susceptibility data leads to a Heisenberg model based on three significant antiferromagnetic exchange interactions, with values of 173.7 cm-1 in the {Fe3O} triangle, and 30.9 and 19.1 cm-1 within the {Fe6O3} section, while the exchange between them is <1 cm-1. With these assignments, the theoretical low-temperature differential susceptibility is also in very good agreement with measurements up to 50 T. Magnetic measurements in the milli-kelvin range reveal striking hysteresis loops and magnetization reversals associated with a Landau-Zener-Stückelberg (LZS) transition as enhanced by the occurrence of a phonon bottleneck. 相似文献
955.
Xiaojing Wang Chen Lv Momoji Kubo Akira Miyamoto 《Journal of organometallic chemistry》2006,691(4):551-556
This work reported the investigation of the structural distortions and charge-transfer processes that occurred in the complex of cuprous(I) bis-2,9-dimethyl-1,10-phenanthroline upon oxidation to copper(II), , through a excited state of by density functional theory. The intramolecular electronic transfer from central metal-to-ligand (MLCT) upon the irradiation of light energy is confirmed. Due to this MLCT excitation, the structure of the excited state of is distorted and reorganized to adapt with the change of charge in central metal. As a result, the excited state of is formed, which has the similar electronic and structural properties with . The bulky substituents in 2- and 9-positions of the phenanthroline ligands can restrain the structural distort and decrease nonradiative decay rate. Thus, the electronic and steric effects of the ligands in the cuprous photo-sensitive complexes have important consequences in the behavior of their excited state. 相似文献
956.
Nobuhiro Kanomata Shinsuke Yamada Akira Fusano Jun Oikawa Fumio Sudo 《Tetrahedron》2006,62(17):4128-4138
Synthesis of various bridged nicotinates 6 having [n](2,5)pyridinophane skeletons (n=8-14) was accomplished by the unique pyridine-formation reaction of methyl propiolate with a series of formyl-substituted (vinylimino)phosphoranes 5, which were prepared from the corresponding cycloalkanones 1 via Vilsmeier-Haack formylation giving chloro-substituted cycloalkenals 2, their thermal and photochemical transformation to formyl azirines 4, and the following ring-opening reactions with triphenylphosphine. The HPLC analysis of [11](2,5)pyridinophane derivatives, (Sp,S)-14 and (Rp,S)-14, showed that these diastereomers rapidly epimerize themselves at room temperature and that their planar-chirality was thermodynamically less stable as compared to the corresponding [11](2,5)cyclophane systems. 相似文献
957.
Shirokura N Nakajima K Nakabayashi A Lu D Hara M Domen K Tatsumi T Kondo JN 《Chemical communications (Cambridge, England)》2006,(20):2188-2190
Ordered mesoporous transition metal oxides were successfully crystallized after strengthening the amorphous framework by a silica layer, which efficiently protected the original mesoporous structure against crystallization and resulting mass transfer. 相似文献
958.
Narumi T Niida A Tomita K Oishi S Otaka A Ohno H Fujii N 《Chemical communications (Cambridge, England)》2006,(45):4720-4722
By a novel one-pot reaction sequence involving consecutive organocopper-mediated reduction, transmetalation and asymmetric alkylation, a highly diastereoselective synthesis of functionalized (Z)-fluoroalkene dipeptide isosteres was achieved in good to excellent yields. 相似文献
959.
Deng W Onji T Yamaguchi H Ikeda N Harada A 《Chemical communications (Cambridge, England)》2006,(40):4212-4214
Photoinduced electron transfer between a porphyrin and a new guest cyclodextrin bearing viologen occurs by a supramolecular formation with conformational change of a guest molecule. 相似文献
960.
Three hydroxylated metabolites of 2-propyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-ylmethyl]-5,6,7,8-tetrahydro-3H-cycloheptimidazol-4-one (Pratosartan), which is a selective angiotensin II receptor antagonist, were synthesized in confirmation of their structures and in studies of their pharmacological properties. An MTPA ester of the human main metabolite was identified with the synthesized compound by comparing (1)H-NMR spectra, MS spectra, and HPLC retention time. The structure of the human main metabolite was confirmed to be (S)-(-)-2-(1-hydroxypropyl)-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-ylmethyl]-5,6,7,8-tetrahydro-3H-cycloheptimidazol-4-one ((S)-(-)-1). Also, the rat main metabolites were confirmed to be 8-hydroxylated compound (2) and 5-hydroxylated compound (3). These metabolites showed lower antagonistic activity than that of the parent compound. 相似文献