Abstract
1,6,20,25‐Tetraaza[6.1.6.1]paracyclophane‐13,32‐disulfone D was synthesized under a very dilute condition by the cyclization between tetramethylene dibromide and N,N′‐di‐p‐tosylaminodiphenylsulfone B, which was prepared using N,N′‐diaminodiphenyl sulfone and p‐toluenesulfonyl as raw materials. 1,6,20,25‐Tetra‐sulfoferrocene‐1,6,20,25‐tetraaza[6.1.6.1]paracyclophane‐13,32‐disulfone E was prepared by modifying D with the bioactive unit ferrocene. The structures were confirmed by IR, 1H NMR, and elemental analysis.
Acknowledgments
The authors thank the Chinese National Natural Science Foundation (No. 20572085) and Shannxi Science Foundation (No. 2005B20) for financial support.