1. Coordination-Driven Face-Directed Self-Assembly of Trigonal Prisms. Face-Based Conformational Chirality.
- Author
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Caskey, Douglas C., Yamamoto, Takuya, Addicott, Chris, Shoemaker, Richard K., Vacek, Jaroslav, Hawkridge, Adam M., Muddiman, David C., Kottas, Gregg S., Michi, Josef, and Stang, Peter J.
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NITROMETHANE , *MASS spectrometry , *PYRIDINE , *CHIRALITY , *PRISMS - Abstract
The coordination-driven self-assembly of four different trigonal prisms from 3 equiv of one of four different tetrapyridyl star connectors and 6 equiv of a platinum linker dication in nitromethane is presented. This face-directed approach affords high yields without template assistance. The prisms have been characterized by multinuclear and DOSY NMR and dual ESI-FT-ICR mass spectrometry. The use of a conformationally chiral star connector leads to a conformationally chiral prism when connector arm ends attached to a vertex have a strongly correlated twist sense and chirality is communicated across polyhedral faces, edges, and vertices. Molecular mechanics results suggest that in the smallest prism 3d collective effects dominate and the all-P and all-M conformers are strongly favored. NMR data prove that the two edges of the pyridine rings in the triflate salts of 3a-3d are distinct. An Eyring plot of rates obtained from line-shape analysis and 1-D EXCHSY NMR yields an activation enthalpy ΔH‡ of ~12 kcal/mol and activation entropy ΔS‡ of ~-15 cal/mol·K for the edge interconversion process, compatible with pyridine rotation around the Pt-N bond. For 3c, this behavior is observed only up to ~318 K. At higher temperatures, the Eyring plot is again linear but follows a very different straight line, with a ΔH‡ of ~35 kcal/mol and ΔS‡ of ~60 cal/mol·K. This highly unusual result is further investigated and discussed in the following companion paper. [ABSTRACT FROM AUTHOR]
- Published
- 2008
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