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Pyridine vs. Bipyridine Coordination in PtCl2 Complexes of 4-tButyl-4'-(4-pyridinyl)-2,2'-bipyridine

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Zeitschrift für anorganische und allgemeine Chemie. 2013, 639(14), pp. 2565-2574. ISSN 0044-2313. eISSN 1521-3749. Available under: doi: 10.1002/zaac.201300139

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The reaction of the new terpyridine ligand 4-tbutyl-4'-(4-pyridinyl)-2, 2'-bipyridine L with various sources of “PtCl2” selectively yields either trans-[PtCl2(L)2] (1) with L bonded in a monodentate fashion via its pendant 4-pyridyl ring or cis-[PtCl2(L)] (2), where L coordinates in a bidentate fashion through its 2,2'-bipyridine subunit. The molecular structures of L and of complex 1 were determined by X-ray crystallography and exhibit intra- and intermolecular hydrogen bonding. We have also converted the dichloro complex 2 into the bis(coumarin thiolate) complex 3. Owing to their free imine coordination sites, complexes 1–3 constitute interesting building blocks for multimetal structures in a “complexes as ligands” approach. The reductive behaviour of L and of complexes 1–3 has been investigated by cyclic and square wave voltammetry.

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ISO 690RANK, Matthias, Manfred ZABEL, Rainer F. WINTER, 2013. Pyridine vs. Bipyridine Coordination in PtCl2 Complexes of 4-tButyl-4'-(4-pyridinyl)-2,2'-bipyridine. In: Zeitschrift für anorganische und allgemeine Chemie. 2013, 639(14), pp. 2565-2574. ISSN 0044-2313. eISSN 1521-3749. Available under: doi: 10.1002/zaac.201300139
BibTex
@article{Rank2013Pyrid-24570,
  year={2013},
  doi={10.1002/zaac.201300139},
  title={Pyridine vs. Bipyridine Coordination in PtCl<sub>2</sub> Complexes of 4-<sup>t</sup>Butyl-4'-(4-pyridinyl)-2,2'-bipyridine},
  number={14},
  volume={639},
  issn={0044-2313},
  journal={Zeitschrift für anorganische und allgemeine Chemie},
  pages={2565--2574},
  author={Rank, Matthias and Zabel, Manfred and Winter, Rainer F.}
}
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    <dcterms:abstract xml:lang="eng">The reaction of the new terpyridine ligand 4-tbutyl-4'-(4-pyridinyl)-2, 2'-bipyridine L with various sources of “PtCl2” selectively yields either trans-[PtCl2(L)2] (1) with L bonded in a monodentate fashion via its pendant 4-pyridyl ring or cis-[PtCl2(L)] (2), where L coordinates in a bidentate fashion through its 2,2'-bipyridine subunit. The molecular structures of L and of complex 1 were determined by X-ray crystallography and exhibit intra- and intermolecular hydrogen bonding. We have also converted the dichloro complex 2 into the bis(coumarin thiolate) complex 3. Owing to their free imine coordination sites, complexes 1–3 constitute interesting building blocks for multimetal structures in a “complexes as ligands” approach. The reductive behaviour of L and of complexes 1–3 has been investigated by cyclic and square wave voltammetry.</dcterms:abstract>
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