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RESEARCH PRODUCT
Rational design of covalently bridged [FeIII2MIIO] clusters
Pablo AlborésPablo AlborésEva Rentschlersubject
ChemistryOtras Ciencias Químicasbasic carboxylateCiencias QuímicasRational designSupramolecular chemistrybipyrimidineInorganic Chemistrycovalently linkComputational chemistryCovalent bondAntiferromagnetismmagnetic propertiesSpin (physics)CIENCIAS NATURALES Y EXACTASdescription
We are reporting the first supramolecular dimeric units of basic carboxylates. The neutral [FeIII 2MIIO] motif for different 3d M metals is covalently bound through 2,2′-bipyrimidine. We have structurally characterized the hexanuclear clusters and the related trinuclear building blocks. Their magnetic properties have been fully analyzed and DFT calculations have been performed as a supplementary tool. All results evidence a weak antiferromagnetic interaction through the bpym bridge between isolated spin ground states (in some examples) arising from intra-Fe 2MO core exchange couplings. Fil: Alborés, Pablo. Johannes Gutenberg Universitat Mainz; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Rentschler, Eva. Johannes Gutenberg Universitat Mainz; Alemania
year | journal | country | edition | language |
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2010-03-01 | Dalton Transactions |