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Macrocyclic bis(ureas) as ligands for anion complexation

Two macrocyclic bis(ureas) 1 and 2, both based on diphenylurea, have been synthesized. Compound 1 represents the smaller ring with two ethynylene groups as linkers and 2 the larger ring with two butadiynylene groups. On thermal treatment to 130 °C molecule 1 splits up into two dihydroindoloquinolino...

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Autores principales: Kretschmer, Claudia, Dittmann, Gertrud, Beck, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4142877/
https://www.ncbi.nlm.nih.gov/pubmed/25161744
http://dx.doi.org/10.3762/bjoc.10.193
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author Kretschmer, Claudia
Dittmann, Gertrud
Beck, Johannes
author_facet Kretschmer, Claudia
Dittmann, Gertrud
Beck, Johannes
author_sort Kretschmer, Claudia
collection PubMed
description Two macrocyclic bis(ureas) 1 and 2, both based on diphenylurea, have been synthesized. Compound 1 represents the smaller ring with two ethynylene groups as linkers and 2 the larger ring with two butadiynylene groups. On thermal treatment to 130 °C molecule 1 splits up into two dihydroindoloquinolinone (3) molecules. Both compounds 1 and 2 form adducts with polar molecules such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF) and act as complexing agents towards a series of anions (Cl(−), Br(−), I(−), NO(3)(−), HSO(4)(−)). The crystal structures of 3, 2·2DMSO, 2·2DMF, and of the complex NEt(4)[Br·2] have been determined. Quantitative investigations of the complexation equilibria were performed via (1)H NMR titrations. While 1 is a rather weak complexing agent, the large ring of 2 binds anions with association constants up to log K = 7.93 for chloride ions.
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spelling pubmed-41428772014-08-26 Macrocyclic bis(ureas) as ligands for anion complexation Kretschmer, Claudia Dittmann, Gertrud Beck, Johannes Beilstein J Org Chem Full Research Paper Two macrocyclic bis(ureas) 1 and 2, both based on diphenylurea, have been synthesized. Compound 1 represents the smaller ring with two ethynylene groups as linkers and 2 the larger ring with two butadiynylene groups. On thermal treatment to 130 °C molecule 1 splits up into two dihydroindoloquinolinone (3) molecules. Both compounds 1 and 2 form adducts with polar molecules such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF) and act as complexing agents towards a series of anions (Cl(−), Br(−), I(−), NO(3)(−), HSO(4)(−)). The crystal structures of 3, 2·2DMSO, 2·2DMF, and of the complex NEt(4)[Br·2] have been determined. Quantitative investigations of the complexation equilibria were performed via (1)H NMR titrations. While 1 is a rather weak complexing agent, the large ring of 2 binds anions with association constants up to log K = 7.93 for chloride ions. Beilstein-Institut 2014-08-12 /pmc/articles/PMC4142877/ /pubmed/25161744 http://dx.doi.org/10.3762/bjoc.10.193 Text en Copyright © 2014, Kretschmer et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Kretschmer, Claudia
Dittmann, Gertrud
Beck, Johannes
Macrocyclic bis(ureas) as ligands for anion complexation
title Macrocyclic bis(ureas) as ligands for anion complexation
title_full Macrocyclic bis(ureas) as ligands for anion complexation
title_fullStr Macrocyclic bis(ureas) as ligands for anion complexation
title_full_unstemmed Macrocyclic bis(ureas) as ligands for anion complexation
title_short Macrocyclic bis(ureas) as ligands for anion complexation
title_sort macrocyclic bis(ureas) as ligands for anion complexation
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4142877/
https://www.ncbi.nlm.nih.gov/pubmed/25161744
http://dx.doi.org/10.3762/bjoc.10.193
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