The effect of pressure and substituents on the size of pseudo-macrocyclic cavities in salicylaldoxime ligands

Peter A. Wood, Ross S. Forgan, Alistair R. Lennie, Simon Parsons, Elna Pidcock, Peter A. Tasker, John E. Warren

Research output: Contribution to journalArticlepeer-review

Abstract

The effect of pressure on the crystal structures of 3-chloro-, 3-methoxy-, 3-methyl- and 3-tert-butylsalicylaldoximes has been investigated. The compounds all form the dimeric structure found in salicylaldoxime form I at ambient pressure, which is based on intermolecular hydrogen bonds between the oximic hydrogen and the phenolic oxygen atoms across an inversion centre. These intermolecular interactions, along with intramolecular phenolic hydrogen to oximic nitrogen atom hydrogen bonds form a pseudo-macrocycle with a R-4(4)(10) ring motif. These hydrogen bonding motifs pre-organize an arrangement of four potential donor atoms for a metal cation which, when the phenol groups are deprotonated, provides an N2O22- pocket well suited to the binding of planar transition metal ions. The radius of the cavity defined by the donor atoms in the dimers is dependent on the nature of the 3-substituent, varying from 1.949 angstrom in the 3-methoxy- to 2.037 angstrom in the 3-Bu-t-derivative. Anisotropic compression of the crystals on the application of pressure results in significant changes in the radii of the cavities in the dimers which decrease by ca. 10% at 6 GPa. During compression of the 3-Bu-t-derivative a single crystal to single crystal phase transition was observed between 0.2 and 1.0 GPa to a new polymorph, 3-tert-butylsalicylaldoxime-II. The phase transition produces an increase in symmetry as the space group changes from P-1 to I2/a, but the intermolecular interactions remain essentially unchanged. No phase transitions were observed in the compression of 3-Cl-, 3-Me- or 3-MeO-salicylaldoxime up to 6.2 GPa.

Original languageEnglish
Pages (from-to)239-251
Number of pages13
JournalCrystEngComm
Volume10
Issue number2
DOIs
Publication statusPublished - 2008

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