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Synthesis and Dimerization Studies of a Lipophilic Photoresponsive Aryl‐Extended Tetraurea‐Calix[4]pyrrole

We describe the syntheses of the lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole 1, featuring four appended azo‐phenyl groups with two tert‐butoxy carbonyl meta‐substituents and its photo‐inactive counterpart 2. In CD2Cl2 solutions, both tetraurea‐calix[4]pyrroles self‐assemble int...

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Published in:Chemistry : a European journal 2018-02, Vol.24 (9), p.2182-2191
Main Authors: Sekiya, Ryo, Díaz‐Moscoso, Alejandro, Ballester, Pablo
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description We describe the syntheses of the lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole 1, featuring four appended azo‐phenyl groups with two tert‐butoxy carbonyl meta‐substituents and its photo‐inactive counterpart 2. In CD2Cl2 solutions, both tetraurea‐calix[4]pyrroles self‐assemble into dimeric capsules by encapsulating one molecule of a suitable bis‐N‐oxide or two molecules of a mono‐N‐oxide. The dimeric capsules are mainly stabilized by a cyclic array of sixteen hydrogen bonds established between the eight unidirectionally oriented urea groups. Photoirradiation experiments demonstrated the trans‐to‐cis isomerization of the azo‐phenyl groups and the formation of a plethora of stereo isomeric cis‐azo‐enriched capsular assemblies. The highly cis‐azo enriched capsular assemblies seem to show a reduced stability and their involvement in equilibria with non‐capsular counterparts that also bind the N‐oxides. The thermally induced cis‐to‐trans interconversion processes demonstrated the reversibility of the photoisomerization and the photostability of most binding partners. An equimolar mixture of the two tetraureas produced two homodimeric capsules and the heterodimeric counterpart in a ratio close to statistical distribution. An aryl extension in light: The syntheses of a lipophilic aryl‐extended α,α,α,α‐tetraurea‐phenyl‐calix[4]pyrrole, and its photo‐inactive counterpart are reported. Both tetraureas self‐assemble into dimeric capsules by encapsulating one molecule of a bis‐N‐oxide or two molecules of mono‐N‐oxide. The results of light irradiation experiments performed with the photoresponsive homo‐ and heterocapsules are described.
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subjects Aromatic compounds
Assemblies
Carbonyls
Chemical bonds
Chemistry
Dimerization
host–guest systems
Hydrogen bonding
Hydrogen bonds
Isomerization
Lipophilic
molecular devices
N-Oxides
Oxides
Pyrroles
receptors
self-assembly
supramolecular chemistry
Urea
title Synthesis and Dimerization Studies of a Lipophilic Photoresponsive Aryl‐Extended Tetraurea‐Calix[4]pyrrole
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