The CA.M lattice revisited. Gel formation from a linear bis-isocyanuric acid and 2-amino-4,6-bis-(4-tert-butylphenylamino)-1,3,5-triazine

M. John Plater, James P. Sinclair, Stuart Aiken, Thomas Gelbrich, Michael B. Hursthouse

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

Five bis(isocyanuric) acid dimers have been prepared and characterised. The introduction of flexible alkyl chains was necessary to aid solubility. On mixing with N,N-bis(4-tert-butyphenyl)melamine in THF followed by slow evaporation, a viscous gel can form which is interpreted as evidence for the assembly of an infinite 2-D hydrogen bonded network.

Original languageEnglish
Pages (from-to)6385-6394
Number of pages10
JournalTetrahedron
Volume60
Issue number30
Early online date28 May 2004
DOIs
Publication statusPublished - 19 Jul 2004
Externally publishedYes

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Triazines
Dimers
Solubility
Hydrogen
Evaporation
Gels
melamine
isocyanuric acid

Cite this

Plater, M. John ; Sinclair, James P. ; Aiken, Stuart ; Gelbrich, Thomas ; Hursthouse, Michael B. / The CA.M lattice revisited. Gel formation from a linear bis-isocyanuric acid and 2-amino-4,6-bis-(4-tert-butylphenylamino)-1,3,5-triazine. In: Tetrahedron. 2004 ; Vol. 60, No. 30. pp. 6385-6394.
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The CA.M lattice revisited. Gel formation from a linear bis-isocyanuric acid and 2-amino-4,6-bis-(4-tert-butylphenylamino)-1,3,5-triazine. / Plater, M. John; Sinclair, James P.; Aiken, Stuart; Gelbrich, Thomas; Hursthouse, Michael B.

In: Tetrahedron, Vol. 60, No. 30, 19.07.2004, p. 6385-6394.

Research output: Contribution to journalArticle

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