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Frontispiece: Correlating Solution‐ and Solid‐State Structures of Conformationally Flexible Resorcinarenes: Significance of a Sulfonyl Group in Intramolecular Self‐Inclusion
Author(s) -
Pamuła Małgorzata,
Nissinen Maija,
Helttunen Kaisa
Publication year - 2020
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.202083363
Subject(s) - resorcinarene , intramolecular force , chemistry , solid state , crystallography , sulfonyl , inclusion (mineral) , crystal structure , group (periodic table) , self assembly , stereochemistry , molecule , organic chemistry , alkyl , mineralogy
Does my crystal structure match with the solution conformation? A conformationally flexible resorcinarene macrocycle forms a self‐inclusion complex in the solid state and adopts a similar folded conformation also in solution. The study was performed by using variable temperature (VT) NMR, XRD, and computational methods. For more information, see the Full Paper by K. Helttunen et al. on page 7374 ff.