Nucleobase Aromaticity
Nucleobase Aromaticity is a physicochemical property characterized by the delocalization of π-electrons within the heterocyclic ring systems of nucleobases, conferring enhanced stability, planarity, and characteristic electronic absorption that distinguishes aromatic nucleobases from non-aromatic analogues in the context of nucleic acid structure and reactivity.
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2017–2026
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Physisorption of nucleobases on graphene: Density-functional calculations
S. Gowtham, Ralph H. Scheicher, Rajeev Ahuja et al. · Physical Review B · 2007 · 328 citations · Full text
Natural Sciences, Chemistry, Physics +17
Vincenzo Verdolino, Roberto Cammi, Barbara H. Munk et al. · The Journal of Physical Chemistry B · 2008 · 188 citations
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TU Dortmund University
Dortmund, Germany
7 h-index
24 publications
802 citations

Uppsala University
Uppsala, Sweden
5 h-index
24 publications
1.3K citations
Japan Science and Technology Agency
Tokyo, Japan
2 h-index
7 publications
201 citations
University of Virginia
Charlottesville, United States
2 h-index
4 publications
141 citations

Wrocław University of Science and Technology
Wroclaw, Poland
2 h-index
5 publications
59 citations

University of Trieste
Trieste, Italy
2 h-index
4 publications
138 citations
The University of Osaka
Osaka, Japan
2 h-index
8 publications
197 citations

Centre National de la Recherche Scientifique
Paris, France
2 h-index
5 publications
256 citations
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JACS · 12 publications · 807 citations
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6 publications · 225 citations
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5 publications · 145 citations
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4 publications · 279 citations
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3 publications · 59 citations
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