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作 者:周仕禄[1] 倪中海[1] 袁新华[1] 宗志敏[1] 魏贤勇[1]
机构地区:[1]中国矿业大学化学工程学院,江苏徐州221008
出 处:《燃料化学学报》2001年第1期80-82,共3页Journal of Fuel Chemistry and Technology
基 金:国家自然科学基金! (2 96 76 0 45 )&&
摘 要:The mechanism of Fe- or Ni- catalyzed hydrogenation of 9,10-diphenylanthracene (9,10-DPA) in decalin in the presence of sulfur was investigated. The qualitative and quantitative analyses of reaction products were conducted by GC-MS. The results showed that Fe and Ni mainly catalyzed non-ipso hydrogenation of 9,10-DPA without sulfur, whereas trans-9,10-dihydro-9,10-diphenylanthracene was main product for both iron sulfide- and nickel sulfide-catalyzed reactions, which suggested that hydrogen atoms was primarily transferred to ipso positions and to different sides of anthracene ring in 9,10-DPA. Quite different catalysis between metals and their sulfides should be responsible for the various mechanisms for hydrogen transfer. It is suggested that metals mainly catalyze diatomic hydrogen transfer, whereas their sulfides primarily promote monatomic hydrogen transfer.The mechanism of Fe- or Ni- catalyzed hydrogenation of 9,10-diphenylanthracene (9,10-DPA) in decalin in the presence of sulfur was investigated. The qualitative and quantitative analyses of reaction products were conducted by GC-MS. The results showed that Fe and Ni mainly catalyzed non-ipso hydrogenation of 9,10-DPA without sulfur, whereas trans-9,10-dihydro-9,10-diphenylanthracene was main product for both iron sulfide- and nickel sulfide-catalyzed reactions, which suggested that hydrogen atoms was primarily transferred to ipso positions and to different sides of anthracene ring in 9,10-DPA. Quite different catalysis between metals and their sulfides should be responsible for the various mechanisms for hydrogen transfer. It is suggested that metals mainly catalyze diatomic hydrogen transfer, whereas their sulfides primarily promote monatomic hydrogen transfer.
关 键 词:9 10-二苯蒽 催化加氢 气相色谱-质谱联用 反应机理
分 类 号:O625.154[理学—有机化学] O621.254.1[理学—化学]
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