BIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIES

The reaction of chlorocarbonylferrocene (2) with bridged calix[4]arene macrocyclic compounds, in which two opposite para-positions are connected by an additional aliphatic chain where n = 5 (1a) or n = 8 (1b) respectively, gave the corresponding new redox-active bis-ferrocene derivatives of bridged...

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Main Authors: Beer, P, Keefe, A, Bohmer, V, Goldmann, H, Vogt, W, Lecocq, S, Perrin, M
Format: Journal article
Language:English
Published: 1991
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author Beer, P
Keefe, A
Bohmer, V
Goldmann, H
Vogt, W
Lecocq, S
Perrin, M
author_facet Beer, P
Keefe, A
Bohmer, V
Goldmann, H
Vogt, W
Lecocq, S
Perrin, M
author_sort Beer, P
collection OXFORD
description The reaction of chlorocarbonylferrocene (2) with bridged calix[4]arene macrocyclic compounds, in which two opposite para-positions are connected by an additional aliphatic chain where n = 5 (1a) or n = 8 (1b) respectively, gave the corresponding new redox-active bis-ferrocene derivatives of bridged calix[4]arenes, 3a and 3b. An X-ray diffraction study of 3a shows that the caliz[4]arene has a cone conformation in which the two ferrocene substituents are located on the phenolic units connected to each other by the aliphatic chain bridge. Cyclic voltammetric and coulometric studies in dichloromethane reveal that 3a and 3b undergo reversible two electron oxidations at + 0.90 V (versus SCE), suggesting that the two respective ferrocene moieties are oxidised in one step. Proton NMR complexation studies (CD3CN) showed neither 3a or 3b form solution host-guest complexes with t-butylamine and benzylamine. © 1991.
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spelling oxford-uuid:4e7b0680-4d30-4ec2-8140-66c9311b8d112022-03-26T16:01:25ZBIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIESJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:4e7b0680-4d30-4ec2-8140-66c9311b8d11EnglishSymplectic Elements at Oxford1991Beer, PKeefe, ABohmer, VGoldmann, HVogt, WLecocq, SPerrin, MThe reaction of chlorocarbonylferrocene (2) with bridged calix[4]arene macrocyclic compounds, in which two opposite para-positions are connected by an additional aliphatic chain where n = 5 (1a) or n = 8 (1b) respectively, gave the corresponding new redox-active bis-ferrocene derivatives of bridged calix[4]arenes, 3a and 3b. An X-ray diffraction study of 3a shows that the caliz[4]arene has a cone conformation in which the two ferrocene substituents are located on the phenolic units connected to each other by the aliphatic chain bridge. Cyclic voltammetric and coulometric studies in dichloromethane reveal that 3a and 3b undergo reversible two electron oxidations at + 0.90 V (versus SCE), suggesting that the two respective ferrocene moieties are oxidised in one step. Proton NMR complexation studies (CD3CN) showed neither 3a or 3b form solution host-guest complexes with t-butylamine and benzylamine. © 1991.
spellingShingle Beer, P
Keefe, A
Bohmer, V
Goldmann, H
Vogt, W
Lecocq, S
Perrin, M
BIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIES
title BIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIES
title_full BIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIES
title_fullStr BIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIES
title_full_unstemmed BIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIES
title_short BIS-FERROCENE DERIVATIVES OF BRIDGED CALIX[4]ARENES - SYNTHESIS, X-RAY CRYSTAL-STRUCTURE AND ELECTROCHEMICAL PROPERTIES
title_sort bis ferrocene derivatives of bridged calix 4 arenes synthesis x ray crystal structure and electrochemical properties
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