Cargando…
Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case
The association of substituted benzoates and naphthyridine dianions was used to study the complexation of dibutyltriuret. The title molecule is the simplest molecule able to form two intramolecular hydrogen bonds. The naphthyridine salt was used to break two intramolecular hydrogen bonds at a time w...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660960/ https://www.ncbi.nlm.nih.gov/pubmed/26664631 http://dx.doi.org/10.3762/bjoc.11.227 |
_version_ | 1782402908557410304 |
---|---|
author | Mroczyńska, Karina Kaczorowska, Małgorzata Kolehmainen, Erkki Grubecki, Ireneusz Pietrzak, Marek Ośmiałowski, Borys |
author_facet | Mroczyńska, Karina Kaczorowska, Małgorzata Kolehmainen, Erkki Grubecki, Ireneusz Pietrzak, Marek Ośmiałowski, Borys |
author_sort | Mroczyńska, Karina |
collection | PubMed |
description | The association of substituted benzoates and naphthyridine dianions was used to study the complexation of dibutyltriuret. The title molecule is the simplest molecule able to form two intramolecular hydrogen bonds. The naphthyridine salt was used to break two intramolecular hydrogen bonds at a time while with the use of substituted benzoates the systematic approach to study association was achieved. Both, titrations and variable temperature measurements shed the light on the importance of conformational equilibrium and its influence on association in solution. Moreover, the associates were observed by mass spectrometry. The DFT-based computations for complexes and single bond rotational barriers supports experimental data and helps understanding the properties of multiply hydrogen bonded complexes. |
format | Online Article Text |
id | pubmed-4660960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-46609602015-12-09 Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case Mroczyńska, Karina Kaczorowska, Małgorzata Kolehmainen, Erkki Grubecki, Ireneusz Pietrzak, Marek Ośmiałowski, Borys Beilstein J Org Chem Full Research Paper The association of substituted benzoates and naphthyridine dianions was used to study the complexation of dibutyltriuret. The title molecule is the simplest molecule able to form two intramolecular hydrogen bonds. The naphthyridine salt was used to break two intramolecular hydrogen bonds at a time while with the use of substituted benzoates the systematic approach to study association was achieved. Both, titrations and variable temperature measurements shed the light on the importance of conformational equilibrium and its influence on association in solution. Moreover, the associates were observed by mass spectrometry. The DFT-based computations for complexes and single bond rotational barriers supports experimental data and helps understanding the properties of multiply hydrogen bonded complexes. Beilstein-Institut 2015-11-05 /pmc/articles/PMC4660960/ /pubmed/26664631 http://dx.doi.org/10.3762/bjoc.11.227 Text en Copyright © 2015, Mroczyńska 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 Mroczyńska, Karina Kaczorowska, Małgorzata Kolehmainen, Erkki Grubecki, Ireneusz Pietrzak, Marek Ośmiałowski, Borys Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case |
title | Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case |
title_full | Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case |
title_fullStr | Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case |
title_full_unstemmed | Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case |
title_short | Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case |
title_sort | conformational equilibrium in supramolecular chemistry: dibutyltriuret case |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660960/ https://www.ncbi.nlm.nih.gov/pubmed/26664631 http://dx.doi.org/10.3762/bjoc.11.227 |
work_keys_str_mv | AT mroczynskakarina conformationalequilibriuminsupramolecularchemistrydibutyltriuretcase AT kaczorowskamałgorzata conformationalequilibriuminsupramolecularchemistrydibutyltriuretcase AT kolehmainenerkki conformationalequilibriuminsupramolecularchemistrydibutyltriuretcase AT grubeckiireneusz conformationalequilibriuminsupramolecularchemistrydibutyltriuretcase AT pietrzakmarek conformationalequilibriuminsupramolecularchemistrydibutyltriuretcase AT osmiałowskiborys conformationalequilibriuminsupramolecularchemistrydibutyltriuretcase |