A radically configurable six-state compound.

نویسندگان

  • Jonathan C Barnes
  • Albert C Fahrenbach
  • Dennis Cao
  • Scott M Dyar
  • Marco Frasconi
  • Marc A Giesener
  • Diego Benítez
  • Ekaterina Tkatchouk
  • Oleksandr Chernyashevskyy
  • Weon Ho Shin
  • Hao Li
  • Srinivasan Sampath
  • Charlotte L Stern
  • Amy A Sarjeant
  • Karel J Hartlieb
  • Zhichang Liu
  • Raanan Carmieli
  • Youssry Y Botros
  • Jang Wook Choi
  • Alexandra M Z Slawin
  • John B Ketterson
  • Michael R Wasielewski
  • William A Goddard
  • J Fraser Stoddart
چکیده

Most organic radicals possess short lifetimes and quickly undergo dimerization or oxidation. Here, we report on the synthesis by radical templation of a class of air- and water-stable organic radicals, trapped within a homo[2]catenane composed of two rigid and fixed cyclobis(paraquat-p-phenylene) rings. The highly energetic octacationic homo[2]catenane, which is capable of accepting up to eight electrons, can be configured reversibly, both chemically and electrochemically, between each one of six experimentally accessible redox states (0, 2+, 4+, 6+, 7+, and 8+) from within the total of nine states evaluated by quantum mechanical methods. All six of the observable redox states have been identified by electrochemical techniques, three (4+, 6+, and 7+) have been characterized by x-ray crystallography, four (4+, 6+, 7+, and 8+) by electron paramagnetic resonance spectroscopy, one (7+) by superconducting quantum interference device magnetometry, and one (8+) by nuclear magnetic resonance spectroscopy.

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عنوان ژورنال:
  • Science

دوره 339 6118  شماره 

صفحات  -

تاریخ انتشار 2013