• Bulletin of the Korean Chemical Society
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• 제26권6호
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• pp.887-891
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• 2005

Novel nickel catalyst deposited on nanoporous carbon was found to be an efficient catalyst for the epoxidation of simple alkenes with $O_2$ and isobutyraldehyde under mild conditions. Alkenes exhibited different reactivities towards Ni-catalyst and epoxidation with stilbene proceeds stereospecifically. This may be rationalized with the mechanism involving coordinated acylperoxy radical intermediate. Nickel contents depend on the preparative methods and the KNI-3 catalyst, which was synthesized by wet impregnation of $Ni(NO_3)_2$ into nanoporous carbon, shows the highest activity. The activity of the catalyst is well correlated with contents of nickel. Recycled catalysts suffer considerable loss of activity due to leaching of catalytic active species, nickel.

• 대한화학회지
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• 제46권2호
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• pp.139-144
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• 2002

니켈 착물을 촉매로 사용한 1,1´-Bis(dimethylsilyl)ferrocene [1]과 carbonyl 화합물 -benzaldehyde, 4-cyanobenzaldehyde, trimethylacetaldehyde, acetophenone과 benzophenone-은 3-oxa-2,5-disilacyclo-1,1′-ferrocene을 생성하였다. 이와 대비되게 동일한 반응조건에서 화합물 [1]과 isobutyraldehyde의 반응에는 1,1′-bis(dimethylsilyl)ferrocene의 Si-H 결합에 2개의 aldehyde ligand가 이중 삽입된 생성물이 형성되었다.