2-Amidopyrroles and 2,5-diamidopyrroles as simple anion binding Agents

P.A. Gale; S. Camiolo; G.J. Tizzard; C.P. Chapman; M.E. Light; S.J. Coles; M.B. Hursthouse

doi:10.1021/jo016020g

2-Amidopyrroles and 2,5-diamidopyrroles as simple anion binding Agents

P.A. Gale
, S. Camiolo
, G.J. Tizzard
, C.P. Chapman
, M.E. Light
, S.J. Coles
, M.B. Hursthouse

Research output: Contribution to journal › Article › Academic › peer-review

99 Citations (Scopus)

Abstract

Four new 2-amidopyrroles and 2,5-diamidopyrroles have been synthesized and their anion complexation properties investigated. The crystal structures of these receptors have been elucidated and reveal hydrogen bonding in the solid state leading to dimer and network formation. Selectivity for oxo-anions has been demonstrated by 1H NMR titration techniques.

Original language	English
Pages (from-to)	7849-7853
Journal	Journal of Organic Chemistry
Volume	66
Issue number	23
DOIs	https://doi.org/10.1021/jo016020g
Publication status	Published - 16-Nov-2001
Externally published	Yes

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abstract = "Four new 2-amidopyrroles and 2,5-diamidopyrroles have been synthesized and their anion complexation properties investigated. The crystal structures of these receptors have been elucidated and reveal hydrogen bonding in the solid state leading to dimer and network formation. Selectivity for oxo-anions has been demonstrated by 1H NMR titration techniques.",

author = "P.A. Gale and S. Camiolo and G.J. Tizzard and C.P. Chapman and M.E. Light and S.J. Coles and M.B. Hursthouse",

year = "2001",

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AU - Gale, P.A.

AU - Camiolo, S.

AU - Tizzard, G.J.

AU - Chapman, C.P.

AU - Light, M.E.

AU - Coles, S.J.

AU - Hursthouse, M.B.

PY - 2001/11/16

Y1 - 2001/11/16

N2 - Four new 2-amidopyrroles and 2,5-diamidopyrroles have been synthesized and their anion complexation properties investigated. The crystal structures of these receptors have been elucidated and reveal hydrogen bonding in the solid state leading to dimer and network formation. Selectivity for oxo-anions has been demonstrated by 1H NMR titration techniques.

AB - Four new 2-amidopyrroles and 2,5-diamidopyrroles have been synthesized and their anion complexation properties investigated. The crystal structures of these receptors have been elucidated and reveal hydrogen bonding in the solid state leading to dimer and network formation. Selectivity for oxo-anions has been demonstrated by 1H NMR titration techniques.

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M3 - Article

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JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 23

ER -

2-Amidopyrroles and 2,5-diamidopyrroles as simple anion binding Agents

Abstract

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