Mono- and ditopic hydroxamate ligands towards discrete and extended network architectures

  • Mohammed B. Fugu
  • , Rebecca J. Ellaby
  • , Helen M. O`Connor
  • , Mateusz B. Pitak
  • , Wim Klooster
  • , Peter N. Horton
  • , Simon J. Coles
  • , Mohammed H. Al-mashhadani
  • , Euan K. Brechin
  • , Igor Perepichka
  • , Leigh F. Jones

Research output: Contribution to journalArticlepeer-review

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Abstract

A family of mono- and ditopic hydroxamic acids have been employed in the synthesis, structural and physical characterisation of discrete (0D) and (1- and 2-D) extended network coordination complexes. Examples of the latter include the 1-D coordination polymer {[Zn(II)(L3H)2]·2MeOH}n (5; L3H2 = 2-(methylamino)phenylhydroxamic acid) and the 2-D extended network {[Cu(II)(L2H)(H2O)(NO3)]·H2O}n (5; L2H2 = 4-amino-2-(acetoxy)phenylhydroxamic acid). The 12-MC-4 metallacrown [Cu(II)5(L4H)4(MeOH)2(NO3)2]·3H2O.4MeOH (7) represents the first metal complex constructed using the novel ligand N-hydroxy-2-[(2-hydroxy-3-methoxybenzyl)amino]benzamide (L4H3). Variable temperature magnetic susceptibility studies confirm strong antiferromagnetic exchange between the Cu(II) centres in 7. Coordination polymer 5 shows photoluminescence in the blue region (λPL ~ 421 – 450 nm) with a bathochromic shift of the emission (~ 15 – 30 nm) from solution to the solid state.
Original languageEnglish
Pages (from-to)10180-10190
JournalDalton Transactions
Volume48
Issue number27
Early online date4 Jun 2019
DOIs
Publication statusPublished - Jul 2019

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