J. Am. Chem. Soc., 130 (3), 836 -838, 2008. 10.1021/ja077661h S0002-7863(07)07661-5
Web Release Date: December 29, 2007

Copyright © 2007 American Chemical Society

Coordinative Self-Assembly and Solution-Phase X-ray Structural Characterization of Cavity-Tailored Porphyrin Boxes

Suk Joong Lee, Karen L. Mulfort, Xiaobing Zuo, Andrew J. Goshe, Paul J. Wesson, SonBinh T. Nguyen, Joseph T. Hupp,* and David M. Tiede

Departments of Chemistry and Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, and Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439

j-hupp@northwestern.edu

Received October 4, 2007

Abstract:

Combining linear Zn porphyrin trimers with orthogonally derivatized porphyrin dimers leads rapidly and spontaneously to the formation of monodisperse, torsionally constrained boxes comprising six components and a total of 16 metalloporphyrins. In situ X-ray scattering measurements confirm the formation of monodisperse assemblies of precisely the size expected from model box structures. While simple subunits yield highly symmetrical boxes, we find that sterically demanding subunits produce unusual twisted boxes. Previous studies of porphyrin-based box-like assemblies (squares) for selective catalysis and molecular sieving revealed two function-inhibiting structural problems: torsional motion along the metal-porphyrin-metal axis and ambiguous outside versus inside functionalization (via axial ligation of available Zn(II) sites). The new 16-porphyrin box assemblies eliminate both problems.


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