Confirmation of a ‘cleft-mode’ of binding in a 2,5-diamidopyrrole anion receptor in the solid state.
Confirmation of a ‘cleft-mode’ of binding in a 2,5-diamidopyrrole anion receptor in the solid state.
The crystal structure of the tetrabutylammonium benzoate complex of 3,4-diphenyl-1H-pyrrole-2,5-dicarboxylic acid bis-butylamide has been elucidated confirming the formation of a cleft conformation in the solid state upon anion binding.
crystallography, benzoate, anion binding, supramolecular chemistry
6995-6996
Camiolo, Salvatore
4ea1c6a7-c0c9-48a0-8998-66a61de7d4d0
Gale, Philip A.
ce0aa62f-d081-408b-8b00-6d954058afab
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Light, Mark E.
13b5eb33-3114-4fb7-8500-90ce69e9933c
2002
Camiolo, Salvatore
4ea1c6a7-c0c9-48a0-8998-66a61de7d4d0
Gale, Philip A.
ce0aa62f-d081-408b-8b00-6d954058afab
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Light, Mark E.
13b5eb33-3114-4fb7-8500-90ce69e9933c
Camiolo, Salvatore, Gale, Philip A., Hursthouse, Michael B. and Light, Mark E.
(2002)
Confirmation of a ‘cleft-mode’ of binding in a 2,5-diamidopyrrole anion receptor in the solid state.
Tetrahedron Letters, 43, .
(doi:10.1016/S0040-4039(02)01581-2).
Abstract
The crystal structure of the tetrabutylammonium benzoate complex of 3,4-diphenyl-1H-pyrrole-2,5-dicarboxylic acid bis-butylamide has been elucidated confirming the formation of a cleft conformation in the solid state upon anion binding.
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Published date: 2002
Keywords:
crystallography, benzoate, anion binding, supramolecular chemistry
Identifiers
Local EPrints ID: 13526
URI: http://eprints.soton.ac.uk/id/eprint/13526
ISSN: 0040-4039
PURE UUID: 24388930-a440-47a9-abc6-875057edb2cb
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Date deposited: 14 Dec 2004
Last modified: 15 Mar 2024 05:07
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Contributors
Author:
Salvatore Camiolo
Author:
Philip A. Gale
Author:
Mark E. Light
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