Project/Area Number |
09650858
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
触媒・化学プロセス
|
Research Institution | Toyama University |
Principal Investigator |
TAKAYASU Osamu (1998) Toyama University, Department of Science, Professor, 理学部, 教授 (40019188)
大澤 力 (1997) 富山大学, 理学部, 助教授 (60213683)
|
Co-Investigator(Kenkyū-buntansha) |
MIYAZAKI Takafumi Toyama University, Department of Science, Research Associate, 理学部, 助手 (70260156)
高安 紀 富山大学, 理学部, 教授 (40019188)
|
Project Period (FY) |
1997 – 1998
|
Project Status |
Completed (Fiscal Year 1998)
|
Budget Amount *help |
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 1998: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1997: ¥2,500,000 (Direct Cost: ¥2,500,000)
|
Keywords | modified metal catalyst / cinconidine modified Pd catalyst / tartaric acid modified nickel catalyst / enantio-differentiating hydrogenation / supported catalyst / tiglic acid / methyl acetoacetate / エナンチオ面区分水素化 |
Research Abstract |
Highly selective enantio-differentiating catalysts were developed in the hydrogenation of prochiral ketones and prochiral alkenes. 1 Enantio-differentiating hydrogenation of prochiral alkenes Investigation of the catalyst preparation conditions and reaction conditions were carried out using tiglic acid as a substrate. Palladium was the best metal for this reaction. Preparation methods used are as follows. (i) decomposition of Pd acetylacetonate, (ii) impregnation using Pd nitrate, (iii) Reduction of impregnated palladium chloride by Sodium Borohydride. alpha-alumina or titania supported Pd catalysts prepared by the third method and modified with cinconidine gave the highest enantiomer excess in the hydrogenation of tiglic acid. 2. Enantio-differentiating hydrogenation of prochiral ketones Supported nickel catalysts were prepared from nickel acetylacetonate, and then modified in a solution containing tartaric acid and NaBr. The effect of the catalyst preparation conditions on optical yield were examined in the enantio-differentiating hydrogenation of methyl acetoacetate. The maximal optical yield of 86% was attained when zeolite was used as the support. XRD and TEM analyses indicated that high optical yields were attained with a nickel crystallite size of about .50 nm.
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