摘要
Fe/activated carbon was found to be catalytically effective for the one-step hydroxylation of several typical substituted aromatic compounds under milder reaction conditions(303 K,atmospheric pressure). It was found that the ring oxidation is predominant for all the substrates studied and the selectivity to ring oxidation was much greater than those reported previously.A comparison of the conversions with that of benzene revealed that electron-donating substituents increase the conversions of the substrates,while electron-withdrawing substituents decrease the conversions.The formation of o-and p-hydroxylated products for electron-donating substituted aromatic compounds and o-,m-,p-hydroxylated products for electron-withdrawing substituted aromatic compounds revealed an electrophilc mechanism.The predominant selectivity to o-hydroxylated products for the aromatic compounds with substituents which could coordianated with Fe also shows a new mechanism.This coordianation was affected by the steric hindrance of the substituents.The latter mechanism was also confirmed by DFT method.
Fe/activated carbon was found to be catalytically effective for the one-step hydroxylation of several typical substituted aromatic compounds under milder reaction conditions (303 K, atmospheric pressure). It was found that the ring oxidation is predominant for all the substrates studied and the selectivity to ring oxidation was much greater than those reported previously. A comparison of the conversions with that of benzene revealed that electron-donating substituents increase the conversions of the substrates, while electron-withdrawing substituents decrease the conversions. The formation of o- and p-hydroxylated products for electron-donating substituted aromatic compounds and o-, m-, p-hydroxylated products for electron-withdrawing substituted aromatic compounds revealed an electrophilc mechanism. The predominant selectivity to o-hydroxylated products for the aromatic compounds with substituents which could coordianated with Fe also shows a new mechanism. This coordianation was affected by the steric hindrance of the substituents. The latter mechanism was also confirmed by DFT method.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2007年第8期1570-1572,共3页
Chemical Journal of Chinese Universities
基金
国家自然科学基金(批准号:20502017)资助
关键词
活性炭(AC)
铁催化剂
羟基化
过氧化氢
芳烃
Activated carbon(AC)
Iron catalyst
Hydroxylation
H2O2
Aromatic hydrocarbons