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Issue 32, 2013
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Spin crossover in Co(II) metallorods – replacing aliphatic tails by aromatic

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Abstract

Terpyridine ligands with ter- and quater-phenyl substituents at the 4′ position provide bis(ligand)Co(II) complexes showing very different magnetic properties to those of their analogues with long-chain aliphatic substituents, with no evidence of “re-entrant” behavior involving multiple high- and low-spin species. Structure determinations of [Co(tptpy)2](BF4)2·CH3OH and [Co(qptpy)2](BPh4)2·3.5dmf·2H2O (dmf = N,N-dimethylformamide) show the metal ion centres in both to be relatively distant and that the “terpyridine embrace” observed to be partially retained in their analogues is completely lost. Consideration of available structural and magnetic data for these and other Co(II) complexes of functionalised terpyridines and terpyridine itself provides evidence that spin crossover behaviour may be regulated by face-to-face contacts of the pyridyl units of the head groups.

Graphical abstract: Spin crossover in Co(ii) metallorods – replacing aliphatic tails by aromatic

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Publication details

The article was received on 29 May 2013, accepted on 25 Jun 2013 and first published on 26 Jun 2013


Article type: Paper
DOI: 10.1039/C3DT51396C
Citation: Dalton Trans., 2013,42, 11507-11521
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    Spin crossover in Co(II) metallorods – replacing aliphatic tails by aromatic

    Y. H. Lee, M. S. Won, J. M. Harrowfield, S. Kawata, S. Hayami and Y. Kim, Dalton Trans., 2013, 42, 11507
    DOI: 10.1039/C3DT51396C

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