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Pentagonal Bipyramidal Ln(III) Complexes Containing an Axial Phosphine Oxide Ligand: Field-induced Single-ion Magnetism Behavior of the Dy(III) Analogues
Author(s) -
Pankaj Kalita,
Naushad Ahmed,
Arun Kumar Bar,
Sourav Dey,
Anukul Jana,
Gopalan Rajaraman,
JeanPascal Sutter,
Vadapalli Chandrasekhar
Publication year - 2020
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.0c00751
Subject(s) - chemistry , pentagonal bipyramidal molecular geometry , lanthanide , phosphine oxide , crystallography , ion , ligand (biochemistry) , magnetism , coordination geometry , oxide , chloride , phosphine , inorganic chemistry , stereochemistry , crystal structure , molecule , catalysis , organic chemistry , biochemistry , physics , receptor , hydrogen bond , quantum mechanics
A series of neutral homologous complexes [(L)Ln(Cy 3 PO)Cl] {where Ln = Gd ( 1 ), Tb ( 2 ), Dy ( 3 ), and Er ( 5 )} and [(L)Dy(Ph 3 PO)Cl] ( 4 ) [H 2 L = 2,6-diacetylpyridine bis -benzoylhydrazone] were isolated. In these complexes, the central lanthanide ion possesses a pentagonal bipyramidal geometry with an overall pseudo D 5 h symmetry. The coordination environment around the lanthanide ion comprises of three nitrogen and two oxygen donors in an equatorial plane. The axial positions are taken up by a phosphine oxide (O donor) and a chloride ion. Among these compounds, the Dy(III) ( 3 and 4 ) analogues were found to be field-induced single-ion magnets.

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