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Guanosine Hydrogen-Bonded Scaffolds: A New Way to Control the Bottom-Up Realisation of Well-Defined Nanoarchitectures

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 15, Issue 32, Pages 7792-7806

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200802506

Keywords

chirality; functional materials; guanosine; self-assembly; supramolecular chemistry

Funding

  1. Italian Ministry in charge of Education
  2. Universities and Research (through PRIN programs)
  3. University of Bologna

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Over the last two decades, guanosine-related molecules have been of interest in different areas, ranging from structural biology to medicinal chemistry, supramolecular chemistry and nanotechnology. The guanine base is a multiple hydrogen-bonding unit, capable also of binding to cations, and fits very well with contemporary studies in supramolecular chemistry, self-assembly and non-covalent synthesis. This Concepts article, after reviewing on the diversification of self-organised assemblies from guanosine-based low-molecular-weight molecules, will mainly focus on the use of guanine moiety as a potential scaffold for designing functional materials of tailored physical properties.

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