4.7 Article

Size selective self-sorting in coordination-driven self-assembly of finite ensembles

Journal

INORGANIC CHEMISTRY
Volume 47, Issue 11, Pages 4706-4711

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ic800038j

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Funding

  1. NIGMS NIH HHS [GM-057052, R01 GM057052, R01 GM057052-31, GM-080820] Funding Source: Medline

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Size selective self-sorting in the coordination-driven self-assembly of two-dimensional (2-D) polygons and three-dimensional (3-D) cages is presented. Two types of polygons (rectangular and triangular) of different size are formed spontaneously from within mixtures of a molecular clip or a 60 degrees organoplatinum acceptor with dipyridyl linkers of different lengths via self-sorting, Furthermore, two different sized 3-D supramolecular cages are formed upon mixing one ditopic organoplatinum acceptor and two different sized tritopic donors from the self-sorting process. The formation of these polygons and cages is characterized using NMR spectroscopy and electrospray ionization mass spectrometry (ESI-MS). In all cases, the self-sorting process is directed by the size of the donor building blocks and a dynamic, thermodynamically driven self-correction process resulting in the formation of discrete products from complex mixtures.

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