Journal
CHEMICAL COMMUNICATIONS
Volume 51, Issue 58, Pages 11677-11680Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc03197d
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Funding
- European Community through the project EC FP7 ICT-MOLARNET [318516]
- European Research Council project SUPRAFUNCTION [GA-257305]
- Agence Nationale de la Recherche through the LabEx project Chemistry of Complex Systems [ANR-10-LABX-0026_CSC]
- International Center for Frontier Research in Chemistry (icFRC)
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We report on the synthesis and self-assembly of three novel lipophilic guanosine derivatives exposing a ferrocene moiety in the C(5') position of the sugar unit. Their self-association in solution, and at the solid/liquid interface, can be tuned by varying the size and nature of the C(8)-substituent, leading to the generation of either G-ribbons, lamellar G-dimer based arrays or the G(4) cation-free architectures.
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