Chemical Shift Tensors in Isomers of Adenine: Relation to Aromaticity of Purine Rings?

Warning

This publication doesn't include Institute of Computer Science. It includes Central European Institute of Technology. Official publication website can be found on muni.cz.
Authors

MALIŇÁKOVÁ Kateřina NOVOSADOVÁ Lucie PIPÍŠKA Matej MAREK Radek

Year of publication 2011
Type Article in Periodical
Magazine / Source ChemPhysChem
MU Faculty or unit

Central European Institute of Technology

Citation
web DOI: 10.1002/cphc.201000657
Doi http://dx.doi.org/10.1002/cphc.201000657
Field Physical chemistry and theoretical chemistry
Keywords solid-state NMR; density-functional theory; X-ray diffraction; nucleus-independent chemical shift; supramolecular cluster
Attached files
Description 13C and 15N chemical shift tensors (CST) are measured, calculated, and compared for three N-benzyladenine isomers with an attempt to characterize differences in electron distribution in the purine ring related to the position of the substituent. Furthermore, the aromaticity of the purine rings is evaluated on the basis of nucleus-independent chemical shifts (NICS), and variations among the isomers are discussed. Both parameters indicate significant differences between the electronic properties of the N3-substituted compound and the N7/N9 pair of structures which can be viewed more generally as the reason for the different stabilities of the individual tautomers.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info