Issue 6, 2014

Comment on “Non-symmetric substituted ureas locked in an (E,Z) conformation: an unusual anion binding via supramolecular assembly” by M. Olivari, C. Caltagirone, A. Garau, F. Isaia, M. E. Light, V. Lippolis, R. Montis and M. A. Scorciapino, New J. Chem., 2013, 37, 663

Abstract

We propose another point of view on the type of hydrogen bonded complexes that were described in this journal (M. Olivari et al., New J. Chem., 2013, 37, 663). The main difference is the molecular geometry and breakage of the intramolecular hydrogen bond during association. The current comment is to highlight mentioned aspects and to point out that in some cases the interpretation may not be straightforward due to the simultaneous effects associated with complexation.

Graphical abstract: Comment on “Non-symmetric substituted ureas locked in an (E,Z) conformation: an unusual anion binding via supramolecular assembly” by M. Olivari, C. Caltagirone, A. Garau, F. Isaia, M. E. Light, V. Lippolis, R. Montis and M. A. Scorciapino, New J. Chem., 2013, 37, 663

Supplementary files

Article information

Article type
Comment
Submitted
16 Oct 2013
Accepted
10 Jan 2014
First published
26 Feb 2014

New J. Chem., 2014,38, 2701-2703

Comment on “Non-symmetric substituted ureas locked in an (E,Z) conformation: an unusual anion binding via supramolecular assembly” by M. Olivari, C. Caltagirone, A. Garau, F. Isaia, M. E. Light, V. Lippolis, R. Montis and M. A. Scorciapino, New J. Chem., 2013, 37, 663

B. Ośmiałowski and E. Kolehmainen, New J. Chem., 2014, 38, 2701 DOI: 10.1039/C3NJ01282D

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