Halogen substituted quinolylsalicylaldimines: Four halogens three structural types

Jitnapa Sirirak, Wasinee Phonsri, David J Harding, Phimphaka Harding, Pimonrat Phommon, Wannapa Chaoprasa, Rebecca M. Hendry, Thomas M. Roseveare, Harry Adams

Research output: Contribution to journalArticleResearchpeer-review

17 Citations (Scopus)

Abstract

A series of halogen substituted 5-X-N-(8-quinolyl)salicylaldimines (HqsalX, X = F 1, Cl 2, Br 3 and I 4) have been prepared, characterized and the crystal structures of all four are reported. The compounds form stacks, in most cases held together either by π-π or lone pair(N)-π interactions. All compounds exhibit an intramolecular OH⋯N hydrogen bond with 2 also displaying an intermolecular OH⋯O hydrogen bonding square. Additional CH⋯N/O and CH⋯π interactions serve to link neighbouring HqsalX molecules with 3 and 4 forming narcissistic dimers. While the halogen has a profound effect on the structure it is not involved in either hydrogen or halogen bonding in any of the structures. DFT calculations suggest that the conformational preference is dependent on the halogen.

Original languageEnglish
Pages (from-to)439-446
Number of pages8
JournalJournal of Molecular Structure
Volume1036
DOIs
Publication statusPublished - 27 Mar 2013
Externally publishedYes

Keywords

  • π-π Stacking
  • DFT calculations
  • Hydrogen bonding
  • Salicylaldimines

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