Guanosine-based hydrogen-bonded 2D scaffolds: Metal-free formation of G-quartet and G-ribbon architectures at the solid/liquid interface
El Garah M, Perone RC, Bonilla AS, Haar S, Campitiello M, Gutierrez R, Cuniberti G, Masiero S, Ciesielski A, Samori P (2015)
Publication Type: Journal article
Publication year: 2015
Journal
Book Volume: 51
Pages Range: 11677-11680
Journal Issue: 58
DOI: 10.1039/c5cc03197d
Abstract
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
Involved external institutions
Université de Strasbourg (UDS)
France (FR)
University of Bologna / Università di Bologna
Italy (IT)
Technische Universität Dresden
Germany (DE)
France (FR)
University of Bologna / Università di Bologna
Italy (IT)
Technische Universität Dresden
Germany (DE)
How to cite
APA:
El Garah, M., Perone, R.C., Bonilla, A.S., Haar, S., Campitiello, M., Gutierrez, R.,... Samori, P. (2015). Guanosine-based hydrogen-bonded 2D scaffolds: Metal-free formation of G-quartet and G-ribbon architectures at the solid/liquid interface. Chemical Communications, 51(58), 11677-11680. https://dx.doi.org/10.1039/c5cc03197d
MLA:
El Garah, Mohamed, et al. "Guanosine-based hydrogen-bonded 2D scaffolds: Metal-free formation of G-quartet and G-ribbon architectures at the solid/liquid interface." Chemical Communications 51.58 (2015): 11677-11680.
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