Macrocyclic Hamilton-type receptors comprising a ferrocene pivot
| Autor: | Holly Roberts, Brice Kauffmann, Brigitte Bibal, Maxime Douarre, Luca Pisciottani, Clotilde Davies, James H. R. Tucker, Sarah L. Horswell, Nathan D. McClenaghan |
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| Přispěvatelé: | Institut des Sciences Moléculaires (ISM), Université Montesquieu - Bordeaux 4-Université Sciences et Technologies - Bordeaux 1-École Nationale Supérieure de Chimie et de Physique de Bordeaux (ENSCPB)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), University of Birmingham [Birmingham], Institut Européen de Chimie et Biologie (IECB), Institut Européen de Chimie et de Biologie, ANR-16-CE29-0011,PETIMIT,Transfert d'électron photoinduit au sein de molécules mécaniquement entrelacées pour l'imagerie de super-résolution et le transport de charges(2016) |
| Rok vydání: | 2018 |
| Předmět: |
[CHIM.ORGA]Chemical Sciences/Organic chemistry
010405 organic chemistry Hydrogen bond ferrocene hydrogen-bonding General Chemistry 010402 general chemistry 01 natural sciences Hamilton receptor 3. Good health 0104 chemical sciences chemistry.chemical_compound Macrocycle Ferrocene chemistry Pyridine Polymer chemistry [CHIM]Chemical Sciences Moiety barbiturate Receptor |
| Zdroj: | Supramolecular Chemistry Supramolecular Chemistry, Taylor & Francis: STM, Behavioural Science and Public Health Titles, 2018, ⟨10.1080/10610278.2018.1426856⟩ |
| ISSN: | 1029-0478 1061-0278 |
| DOI: | 10.1080/10610278.2018.1426856 |
| Popis: | International audience; Synthetic hydrogen-bonding receptors are described, which incorporate a central electroactive ferrocene moiety grafted with two adjacent bis(amido)pyridine motifs and an aliphatic tether (14 and 18 methylene units for 1 and 2, respectively) completing the macrocycle. The crystallographic structure, barbiturate guest-binding studies and electrochemical data are provided for the more strongly-binding macrocycle 2. |
| Databáze: | OpenAIRE |
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