Journal Article FZJ-2018-07492

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Triangular {Ni3} coordination cluster with a ferromagnetically coupled metal-ligand core

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2018
Elsevier Science Amsterdam [u.a.]

Polyhedron 144, 144 - 151 () [10.1016/j.poly.2018.01.014]

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Abstract: The coordination characteristics of a tridentate, π-conjugated Schiff base (HL·SMe) combined with 4-(methylthio)benzoic acid (Hbza·SMe) were explored in methanol solution. A two-step aerobic process involving the precursor NiCl2·6H2O afforded the trinuclear coordination compound [NiII3(L·SMe)4(bza·SMe)(MeOH)2]Cl0.5(CH3O)0.5·5.5MeOH·H2O (1), while the precursor Ni(ClO4)2·6H2O resulted in [NiII3(L·SMe)4(bza·SMe)(MeOH)2](ClO4)0.75(CH3O)0.25·1.5MeOH·0.75H2O (2); in both cases the thioether-containing ligands are key to isolation of crystalline products. Their solvent-free cationic motif [Ni3(L·SMe)4(bza·SMe)]+, supported by two different types of monodeprotonated chelate ligands, has been studied by electrospray ionization mass spectrometry. 1 and 2 crystallize in the triclinic space group and monoclinic space group Cc, respectively, and feature a hitherto not observed triangular metal-ligand skeleton that is characterized by predominantly ferromagnetic exchange coupling between Ni(II) ions. Proof-of-concept infrared reflection–absorption spectroscopy measurements of 1 deposited on a gold substrate indicate that this moisture-stable compound retains its main structural features upon adsorption on the metal surface, which enables subsequent studies of catalytic properties of 1 on a solid support.

Classification:

Contributing Institute(s):
  1. Elektronische Eigenschaften (PGI-6)
  2. JARA-FIT (JARA-FIT)
Research Program(s):
  1. 522 - Controlling Spin-Based Phenomena (POF3-522) (POF3-522)

Appears in the scientific report 2018
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Medline ; Clarivate Analytics Master Journal List ; Current Contents - Physical, Chemical and Earth Sciences ; Ebsco Academic Search ; IF < 5 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2018-12-17, last modified 2021-01-30


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