Unprecedented coupling reactions on (η5-chlorocyclohexadienyl)tricarbonyl manganese complexes with arenes create a new carbon−carbon bond on the conjugated system, keeping intact the η5-chlorocyclohexadienyl moiety; thus, the removal of the exo hydrogen bond of the sp3 CH2 group yields efficiently new cationic (η6-arene) manganese complexes which cannot be prepared directly from the free arene.
上(η前所未有偶联反应5与
芳烃-chlorocyclohexadienyl)三羰基
锰络合物创建该共轭系统在一个新的
碳-
碳键,保持完好的η 5 -chlorocyclohexadienyl部分; 因此,去除的外
SP的
氢键3 CH 2组产量有效地新的阳离子(η 6 -arene),其不能被从自由
芳烃直接制备
锰络合物。