Yoshiki Chujo

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Phosphine is conformationally stable because of the high inversion energy barrier of the phosphorus atom, which allows the phosphorus atom to become a chiral center. Thus, enantiopure P-stereogenic 12-, 15-, 18-, and 21-membered aliphatic phosphines "diphosphacrowns" were synthesized from secondary P-stereogenic bisphosphine as a chiral building block.(More)
The synthesis and analysis of the electronic states of the main-chain type-organogallium polymers are presented. We synthesized the polymers containing four-coordinate gallium atoms by organometal coupling reactions. The synthesized polymers showed good solubility in common organic solvents and enough stability for measuring a series of properties under(More)
Optically active polymers containing P-stereogenic bisphosphine and 1,2,3-triazole units in the main chain were obtained by copper-catalyzed Huisgen cycloaddition. The repeating unit of the polymer adopted bidentate as well as tetradentate coordination, leading to the change in the conformations of the polymer via complexation with transition metals.
The establishment of (19)F NMR signal regulation and the application of this strategy to develop a multi-modal (19)F NMR probe for monitoring enzymatic activity using nanoparticles as a signal regulator is described; water-soluble perfluorinated cubic silsesquioxane was synthesized and immobilized onto the silica nanoparticles for suppressing the signals;(More)
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