Publications by authors named "Atsushi Tahara"

The rapid evolution of antimicrobial resistant genes (AMRs) in water resources is well correlated to the persistent occurrence of ciprofloxacin in water. For the first time, encapsulated nanoscale zerovalent iron (nZVI) with a shell of magnesium hydroxide (Mg/Fe) was used to adsorb ciprofloxacin from water. Optimization of the removal conditions exhibited that 5% was the optimum mass ratio between magnesium hydroxide and nZVI [Mg(OH)/nZVI)] as more than 96% of 100 mg L of ciprofloxacin was removed.

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Radioactive cesium was resealed to the environment as a result of many nuclear incidents. An effective treatment system is urgently needed to safely handle radioactive cesium-contaminated waters. Based on nanoscale zerovalent iron (nZVI) and zeolite, nine adsorbents were synthesized and applied to remove cesium from aqueous solutions.

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High functional group compatibility of iridium-catalyzed synthesis of enamines from amides and 1,1,3,3-tetramethyldisiloxane (TMDS) realized facile access of a series of donor (D)-π-acceptor (A)-conjugated enamines, in which enamine behaves as a donor functional group. The amide precursors containing reducible functional groups, such as halogen, carbonyl, and nitro groups, underwent reaction with TMDS to give the corresponding enamines in high yields. In most cases, chemoselective hydrosilane reduction of the amide group occurred while other reducible groups remained intact.

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A disilaruthenacyclic complex (1) showed extremely high catalytic activity for hydrosilane reduction of aldehydes and ketones to silyl ethers and secondary and tertiary amides to the corresponding amines. An σ-CAM mechanism was proposed to explain the activity.

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Disilaferra- and disilaruthenacyclic complexes containing mesityl isocyanide as a ligand, 3' and 4', were synthesized and characterized by spectroscopy and crystallography. Both 3' and 4' showed excellent catalytic activity for the hydrogenation of alkenes. Compared with iron and ruthenium carbonyl analogues, 1' and 2', the isocyanide complexes 3' and 4' were more robust under the hydrogenation conditions, and were still active even at higher temperatures (∼80 °C) under high hydrogen pressure (∼20 atm).

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The mechanisms associated with the hydrogenation of alkenes catalyzed by the iron complex Fe(cis-CO){o-(SiMe)CH}(H) (1) were investigated by DFT calculations. The complex 1 has a structure in which the iron center is bonded to four silicon atoms and two hydrides. Secondary Si···H···Si interactions were also observed.

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A mixture of an iron or a cobalt carboxylate and an isocyanide ligand catalyzed the hydrosilylation of alkenes with hydrosiloxanes with high efficiency (TON >10(3)) and high selectivity. The Fe catalyst showed excellent activity for hydrosilylation of styrene derivatives, whereas the Co catalyst was widely effective in reaction of alkenes. Both of them catalyzed the reaction with allylic ethers.

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In this article we describe 5 rare cases of mumps-associated pharyngolaryngeal edema. To the best of our knowledge, this report includes the first case of mumps-associated pharyngolaryngeal edema in a patient who had previously received mumps vaccination, and these cases represent the sixth report of mumps-associated pharyngolaryngeal edema in the English literature. All 5 of our patients with mumps infection were adults and manifested airway stenosis due to pharyngolaryngeal edema.

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Deployment of the air bag in a passenger vehicle accident rarely causes otologic injuries. However, sensorineural hearing loss induced by air bag deployment is extremely rare, with only a few cases reported in the English literature. A 38-year-old man involved in a traffic accident while driving his car at 40 km/hour presented with right sensorineural hearing loss and tinnitus, without associated vertigo.

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