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Conformational Flexibility of Tetralactam Macrocycles and Their Intermolecular Hydrogen‐Bonding Patterns in the Solid State
Authors:Sascha S. Zhu Dipl.‐Chem.  Martin Nieger Dr.  Jörg Daniels Dr.  Thorsten Felder Dr.  Iordan Kossev Dr.  Thomas Schmidt Dr.  Moritz Sokolowski Prof. Dr.  Fritz Vögtle Prof. Dr.  Christoph A. Schalley Prof. Dr.
Affiliation:1. Institut für Chemie und Biochemie, Freie Universit?t Berlin, Takustrasse 3, 14195 Berlin (Germany), Fax: (+49)?30‐838‐55817;2. Current address: Kekulé‐Institut für Organische Chemie und Biochemie, Universit?t Bonn, Gerhard‐Domagk‐Strasse 1, 53121 Bonn (Germany);3. Laboratory of Inorganic Chemistry, Department of Chemistry, P.O.Box 55, 00014 University of Helsinki (Finland);4. Institut für Anorganische Chemie, Universit?t Bonn, Gerhard‐Domagk‐Strasse 1, 53121 Bonn (Germany);5. Institut für Physikalische und Theoretische Chemie, Universit?t Bonn, Wegelerstrasse 12, 53115 Bonn (Germany);6. Kekulé‐Institut für Organische Chemie und Biochemie, Universit?t Bonn, Gerhard‐Domagk‐Strasse 1, 53121 Bonn (Germany)
Abstract:Flexible rigidity : Tetralactam macrocycles of the Hunter type bear a rigid scaffold (see space‐filling representation), but can still widely adapt to the properties of a guest molecule inside their cavities. X‐ray crystal structures of a series of differently substituted macrocycles reveal a remarkably broad variety of intermolecular hydrogen‐bonding patterns organizing the macrocycles in the crystals in intriguingly different ways.
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Keywords:conformational flexibility  hydrogen bonds  macrocycles  supramolecular chemistry  tetralactams
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