Wurster's crownophanes: an alternate topology for para-phenylenediamine-based macrocycles
JW Sibert, GR Hundt, AL Sargent, V Lynch
Index: Sibert, John W.; Hundt, Greg R.; Sargent, Andrew L.; Lynch, Vincent Tetrahedron, 2005 , vol. 61, # 52 p. 12350 - 12357
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Citation Number: 14
Abstract
Six redox-active cyclophane/crown hybrid molecules (crownophanes) were prepared via cyclization reactions involving N, N′-dimethyl-p-phenylenediamine and tosylated oligoethylene glycols of varying length. These new host molecules differ from other phenylenediamine-containing crown ethers in that the electron-rich π face is designed to be part of the ligating group. Their electrochemical properties were determined by cyclic ...
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