Volume 47, Issue 40 pp. 7705-7709
Communication

Tunable Molecular Assembly Codes Direct Reaction Pathways

Andrew D. Shaller

Andrew D. Shaller

Department of Chemistry, Washington State University, Pullman, WA (USA), Fax: (+1) 509-335-8867

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Wei Wang Dr.

Wei Wang Dr.

Department of Chemistry, Washington State University, Pullman, WA (USA), Fax: (+1) 509-335-8867

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Haiyang Gan Dr.

Haiyang Gan Dr.

Department of Chemistry, Washington State University, Pullman, WA (USA), Fax: (+1) 509-335-8867

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Alexander D. Q. Li Prof.

Alexander D. Q. Li Prof.

Department of Chemistry, Washington State University, Pullman, WA (USA), Fax: (+1) 509-335-8867

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First published: 22 September 2008
Citations: 86

We acknowledge support from the National Institute of General Medicine Sciences (Grant GM065306), the Mass Spectrometry Core Laboratories at WSU for discussions concerning MALDI data, and the WSU Center for NMR spectroscopy for assistance with variable temperature NMR studies. A.D.Q.L. is a former Beckman Young Investigator (BYI).

Graphical Abstract

In the twist: The extent of twisting from planarity in a series of perylenetetracarboxylic diimides (PDIs) modulates the attractive π–π stacking force, revealing an array of inherent molecular recognition codes. Such coded self-assembly directs specific reaction pathways so that a mixture of reactive monomers with different codes results in identical products as when the reactions were carried out in separate flasks (see picture).

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