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Synthesis and Structures of Homoleptic Monomeric Potassium Aryloxolanthanoidate(III) Complexes
Author(s) -
Deacon Glen B.,
Gitlits Alex,
Junk Peter C.,
Skelton Brian W.,
White Allan H.
Publication year - 2005
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.200400482
Subject(s) - homoleptic , chemistry , lanthanide , monomer , ligand (biochemistry) , potassium , tris , crystallography , hydride , inorganic chemistry , durene , oxygen , medicinal chemistry , stereochemistry , metal , organic chemistry , polymer , ion , biochemistry , receptor , catalysis
Reaction of lanthanoid tris(2, 6‐diphenylphenolates) [Ln(Odpp) 3 ] with KOdpp in 1, 2, 4, 5‐tetramethylbenzene (durene) at 200‐250 °C affords [K{Ln(OC 6 H 3 Ph 2 ‐2, 6) 4 }], (Ln = La ( 1 ) or Nd ( 2 )) and 2 has also been obtained from the reaction of [Nd(Odpp) 3 ] with potassium hydride. In the solid state, 1 and 2 are monomeric bimetallics in which Ln is surrounded by a distorted tetrahedral array of oxygen atoms. Two Odpp ligands are oxygen bridged between K and Ln and also are η 4 ‐Ph linked to potassium. One Odpp ligand bridges the metals in an O(Ln): η 6 ‐Ph(K) manner that is new for lanthanoid complexes of this ligand, with no close K‐O contact, and the remaining Odpp is terminal on the Ln.

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