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Dinucleating Schiff base ligand in Zn/4f coordination chemistry: synthetic challenges and catalytic activity evaluation

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  • Stavroula I Sampani
  • Sidonie Aubert
  • Martin Cattoen
  • Kieran Griffiths
  • Alaa Abdul-Sada
  • Geoffrey R Akien
  • Graham J Tizzard
  • Simon J Coles
  • Stellios Arseniyadis
  • George E Kostakis
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<mark>Journal publication date</mark>7/04/2018
<mark>Journal</mark>Dalton Transactions
Issue number13
Volume47
Number of pages8
Pages (from-to)44786-4493
Publication StatusPublished
Early online date23/02/18
<mark>Original language</mark>English

Abstract

Four Zn/4f polynuclear coordination clusters (PCCs) formulated as [ZnDyL2(CO3)2(NO3)2] (1), [ZnIIYIIIL(NO3)2(o-van) (MeOH)] (MeOH) [2 (MeOH)] and [ZnIILnIIIL(NO3)2Cl(EtOH)] where Ln is Dy (3) and Y (4) and where H2L is the dinucleating Schiff base ligand N,N'-bis(3-methoxysalicylidene)cyclohexane-1,2-diamine and o-van is ortho-vanillin, were prepared and fully characterised for the first time. These air-stable heterometallic PCCs, obtained in high yields from commercially available materials, were shown to remain stable in solution in their dinuclear [ZnIILnIIIL] form. Their catalytic activity was evaluated in various catalytic transformations including the Friedel-Crafts alkylation of 2-acyl imidazoles with indoles.

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This journal is © The Royal Society of Chemistry 2018