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Intra‐ versus Intermolecular Hydrogen Bonding: Solvent‐Dependent Conformational Preferences of a Common Supramolecular Binding Motif from 1 H NMR and Vibrational Circular Dichroism Spectra
Author(s) -
Demarque Daniel P.,
Merten Christian
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201704987
Subject(s) - supramolecular chemistry , hydrogen bond , intermolecular force , circular dichroism , chemistry , crystallography , solvent , motif (music) , spectral line , proton nmr , stereochemistry , molecule , physics , crystal structure , organic chemistry , astronomy , acoustics
Invited for the cover of this issue are Daniel P. Demarque and Christian Merten from Ruhr University in Bochum, Germany. The image depicts a DMSO‐solvated 2,6‐pyridinediyl‐dialkylamide, the model system used in their study to investigate solute‐solvent driven conformational changes. Read the full text of the article at 10.1002/chem.201703643.