Concept
Guanosine Hydrogen-Bonded Scaffolds: A New Way to Control the Bottom-Up Realisation of Well-Defined Nanoarchitectures
Article first published online: 6 MAY 2009
DOI: 10.1002/chem.200802506
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Chemistry - A European Journal
Special Issue: 100th Anniversary of SCI
Volume 15, Issue 32, pages 7792–7806, August 10, 2009
Additional Information
How to Cite
Lena, S., Masiero, S., Pieraccini, S. and Spada, G. P. (2009), Guanosine Hydrogen-Bonded Scaffolds: A New Way to Control the Bottom-Up Realisation of Well-Defined Nanoarchitectures. Chemistry - A European Journal, 15: 7792–7806. doi: 10.1002/chem.200802506
Publication History
- Issue published online: 4 AUG 2009
- Article first published online: 6 MAY 2009
Funded by
- Italian Ministry in charge of Education, Universities and Research
- University of Bologna
- Abstract
- Article
- References
- Cited By
Keywords:
- chirality;
- functional materials;
- guanosine;
- self-assembly;
- supramolecular chemistry
Graphical Abstract

Follow the instructions by guanine! The multiple hydrogen-bonding guanine unit can orient functional groups, giving rise to supramolecular structures with high diversity and potential unprecedented properties (see scheme).
Abstract
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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