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Wiley, Angewandte Chemie International Edition, 1-2(46), p. 198-201, 2007

DOI: 10.1002/anie.200603180

Wiley, Angewandte Chemie, 1-2(119), p. 202-205, 2007

DOI: 10.1002/ange.200603180

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Inclusion of Cavitands and Calix[4]arenes into a Metallobridgedpara-(1H-Imidazo[4,5-f][3,8]phenanthrolin-2-yl)-Expanded Calix[4]arene

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

(Figure Presented) A hunter hunted! A highly preorganized, deep metallocavitand of nanoscale dimensions containing rhenium atoms at the four corners can be readily synthesized from a simple formyl-substituted calix[4]arene and 3,8-phenanthroquinone. Unsubstituted calix[4]arenes and cavitands without substituents on the lower rim are the ideal guests for such an expanded calixarene (see picture), and are included with binding constants of 103-105 M-1.