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Issue 2, 2007
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Supramolecular architectures generated by self-assembly of guanosine derivatives

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Abstract

Nature's use of a simple genetic code to enable life's complex functions is an inspiration for supramolecular chemistry. DNA nucleobases carry the key information utilizing a variety of cooperative and non-covalent interactions such as hydrophobic, van der Waals, π–π stacking, ion–dipole and hydrogen bonding. This tutorial review describes some recent advances in the form and function provided by self-assembly of guanine (G) based systems. We attempt to make connections between the structures of the assemblies and their properties. The review begins with a brief historical context of G self-assembly in water and then describes studies on lipophilic guanosine analogs in organic solvents. The article also focuses on examples of how G analogs have been used as building blocks for functional applications in supramolecular chemistry, material science and nanotechnology.

Graphical abstract: Supramolecular architectures generated by self-assembly of guanosine derivatives

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Publication details

The article was received on 02 Oct 2006 and first published on 07 Nov 2006


Article type: Tutorial Review
DOI: 10.1039/B600282J
Citation: Chem. Soc. Rev., 2007,36, 296-313
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    Supramolecular architectures generated by self-assembly of guanosine derivatives

    J. T. Davis and G. P. Spada, Chem. Soc. Rev., 2007, 36, 296
    DOI: 10.1039/B600282J

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