Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/133548
Title: N,n-dialkylcarbamato lanthanide complexes, a series of isotypical coordination compounds
Authors: Baisch, Ulrich
Dell’Amico, Daniela Belli
Calderazzo, Fausto
Labella, Luca
Marchetti, Fabio
Merigo, Alessandra
Keywords: Magnetic susceptibility
Coordination compounds
Organometallic chemistry
Carbamates
X-ray crystallography
Magnetic susceptibility
Issue Date: 2004
Publisher: Wiley-VCH Verlag GmbH & Co. KGaA
Citation: Baisch, U., Belli Dell’Amico, D., Calderazzo, F., Labella, L., Marchetti, F., & Merigo, A. (2004). N, N‐Dialkylcarbamato Lanthanide Complexes, a Series of Isotypical Coordination Compounds. European journal of inorganic chemistry, 2004(6), 1219-1224.
Abstract: The preparations of the N,N-dialkylcarbamato complexes with analytical formulae [Ln(O2CNR2)3] (Ln = Pr, Nd, Eu, Gd, Ho, Er, Yb, Lu, R = iPr; Ln = Nd, Eu, Gd, R = Bu; Ln = Nd, R = Et), using [LnCl3(ether)x] (ether = THF or dimethoxyethane, DME), NHR2, and CO2 are reported. X-ray diffraction of the diisopropylcarbamato derivatives, including a reinvestigation of [Yb4(O2CNiPr2)12], showed these complexes to be tetranuclear and isotypical over a range of 12 atomic numbers. The lanthanide contraction has been evaluated based on the lengths of four different types of Ln−O bond.
URI: https://www.um.edu.mt/library/oar/handle/123456789/133548
ISSN: 10990682
Appears in Collections:Scholarly Works - FacSciChe

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