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

Mohammed B FuguRebecca J EllabyHelen M O'ConnorMateusz B PitakWim KloosterPeter N HortonSimon J ColesMohammed H Al-MashhadaniIgor F PerepichkaEuan K BrechinLeigh F Jones
Published in: Dalton transactions (Cambridge, England : 2003) (2019)
A family of mono- and ditopic hydroxamic acids has been employed in the synthesis and 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.
Keyphrases
  • solid state
  • photodynamic therapy
  • physical activity
  • mental health
  • aqueous solution
  • risk assessment
  • molecularly imprinted
  • mass spectrometry
  • network analysis
  • liquid chromatography