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Self-Assembly of 2,8,14,20-Tetraisobutyl-5,11,17,23-tetrahydroxyresorc[4]arene

✍ Scribed by Thorsten Gerkensmeier; Waldemar Iwanek; Ceno Agena; Roland Fröhlich; Sirpa Kotila; Christian Näther; Jochen Mattay


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
296 KB
Volume
1999
Category
Article
ISSN
1434-193X

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✦ Synopsis


We report herein the observation of a hexameric structure of only by hydrogen bonds. The tendency to form aggregates in solution is demonstrated mainly by means of ESI-MS a hydroxyresorc [4]arene in the solid state, enclosing a large interior space. This artificial molecular container is stabilized methods.

Olshausenstraße 40, D-24116 Kiel, Germany [b] Institut für Organische Chemie der pädagogischen Hochschule pared both under reflux conditions and at room tempera-Kielce, ture. The product obtained under reflux conditions exhib-Chec ¸insca 5, PL-25Ϫ020 Kielce, Poland [c] Organisch-Chemisches Institut, Westfälische-Wilhelms-Univer-ited simple 1 H-and 13 C-NMR spectra, reflecting the C 4v sität Münster, symmetry, while mass spectrometric data were consistent Corrensstraße 40, D-48149 Münster, Germany with the mass of the expected cyclic tetramer. Crystalliza- [d


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## Abstract In solvents such as chloroform or benzene, tetraurea calix[4]arenes **1** form dimeric capsules in which one solvent molecule is usually included as guest. To explore the structural requirements for the formation of such hydrogen‐bonded dimers we replaced one __p__‐tolylurea residue by