作者:Jan Honzíček、Abhik Mukhopadhyay、Cecilia Bonifacio、Carlos C. Romão
DOI:10.1016/j.jorganchem.2009.11.043
日期:2010.3
The synthesis of new cyclopenta[l]phenanthrenyl complexes [(η5-C17H10Me)(η3-C3H5)Mo(CO)2] and [(η5-C17H9(COOMe)N(CH2)4)(η3-C3H5)Mo(CO)2] is described. Although these compounds are structural analogues their reactivity is different. Protonation of [(η5-C17H10Me)(η3-C3H5)Mo(CO)2] gives a stable ionic compound [(η5-C17H10Me)Mo(CO)2(NCMe)2][BF4] while its analogue containing both tertiary amino and carboxylic
新环戊二烯并[合成升]菲基配合物[(η 5 -C 17 ħ 10 ME)(η 3 -C 3 H ^ 5)的Mo(CO)2 ]和[(η 5 -C 17 ħ 9(COOMe)N (CH 2)4)(η 3 -C 3 H ^ 5)的Mo(CO)2 ]进行说明。尽管这些化合物是结构类似物,但它们的反应性是不同的。[(η的质子化5 -C 17 ħ 10 ME)(η 3 -C 3 H ^5)的Mo(CO)2 ]给出一个稳定的离子性化合物[(η 5 -C 17 ħ 10 Me)中的Mo(CO)2(NCMe)2 ] [BF 4 ],而其同时含有叔胺基和羧酸酯基团[类似物(η 5 -C 17 ħ 9(COOMe)N(CH 2)4)(η 3 -C 3 H ^ 5)的Mo(CO)2 ]相同的条件下分解。[(η 5 -C 17 ħ 10 Me)中的Mo(CO)2(NCMe)2 ] [BF 4]与环戊二烯反应,得到稳定的η