Synthesis of Ruthenium(III) Phthalocyanine with Di-axial Bromo Ligands - A Promising Molecular Conductor with Giant Negative Magnetoresistance

The electron transport of Phthalocyanines (Pc) with central metal and di-axial ligands (such as FeIII(Pc)L2; where L = CN, Cl, Br) originates from its intermolecular Pc π-π orbital overlap while its giant negative magnetoresistance (GNMR) arises from its intramolecular Pc-π(HOMO) and Fe-d (s=1/2) in...

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Bibliographic Details
Main Authors: Mario A.V. Gamboa, Joey A.A. Valinton, Derrick E.C. Yu
Format: Article
Language:English
Published: Growing Science 2015-01-01
Series:Current Chemistry Letters
Subjects:
Online Access:http://www.growingscience.com/ccl/Vol4/ccl_2014_23.pdf
Description
Summary:The electron transport of Phthalocyanines (Pc) with central metal and di-axial ligands (such as FeIII(Pc)L2; where L = CN, Cl, Br) originates from its intermolecular Pc π-π orbital overlap while its giant negative magnetoresistance (GNMR) arises from its intramolecular Pc-π(HOMO) and Fe-d (s=1/2) interaction. However, the π-d interaction tends to localize itinerant electrons resulting in the decrease in the conductivity of the FeIII(Pc)L2 series compared to the non-magnetic CoIII(Pc)L2 where π-d interaction is absent. More so, the axial ligand field energy of the FeIII(Pc)L2 system is found to have the ability to proportionally modulate the π-d interaction. In reference thereof, theoretical calculations point that isostructural RuIII(Pc)Br2 would provide the best balance of π-d orbital energy interplay. That is, RuIII(Pc)Br2 is expected to be a molecule with high electrical conductivity and GNMR which would make it an ideal magnetic molecular conductor. This paper reports on the synthesis of RuIII(Pc)Br2.
ISSN:1927-7296
1927-730X