Resorcarenes in the boat conformation as building blocks for hydrogen-bonded assemblies including two ammonium cations

Chemistry - A European Journal

Volumn 7, Issue 9, 2001, Pages 1944-1951

  Shivanyuk, Alexander ^a,d   Paulus, Erich F ^b   Rissanen, Kari ^a   Kolehmainen, Erkki ^a   Böhmer, Volker ^c  

^a UNIVERSITY OF JYVÄSKYLÄ   (Finland)

^b GOETHE UNIVERSITY   (Germany)

^c JOHANNES GUTENBERG UNIVERSITY   (Germany)

^d SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

Calixarenes; Dimerization; Hydrogen bonds; Inclusion compounds supramolecular chemistry

Indexed keywords

AMMONIA; CRYSTAL STRUCTURE; ENCAPSULATION; ETHANOL; HYDROGEN BONDS; MOLECULES; NEGATIVE IONS;

RESORCARENES;

POSITIVE IONS;

AMMONIA; AMMONIUM DERIVATIVE; CALIXARENE; CHLORIDE ION; CHLORINE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

ARTICLE; CONFORMATION; CRYSTAL STRUCTURE; DIMERIZATION; HYDROGEN BOND; MOLECULAR INTERACTION; SYNTHESIS;

EID: 0035805337     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20010504)7:9<1944::AID-CHEM1944>3.0.CO;2-2     Document Type: Article

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67. The same conformation was also found for 2b and 2c.
68. 1H NMR spectra of resorcarenes and various octa-acylated derivatives showed that the position of the signal for the protons at the 5-positions of the resorcinol rings does not depend significantly on the O substitution.
69. - in which the cation is included in the π basic cavity. The detailed investigation of this complexation will be reported elsewhere.
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