Mixed valency in polynuclear Mn II /Mn III , Mn III /Mn IV and Mn II /Mn III /Mn IV clusters: a foundation for high-spin molecules and single-molecule magnets

Abstract

Mixed-valent Mn/O dinuclear and polynuclear molecular compounds containing Mn III are almost without exception trapped valence. Large differences between the strengths of the exchange interactions within Mn II Mn III , Mn III Mn III and Mn III Mn IV pairs lead to situations where Mn III Mn IV interactions, the strongest of the three mentioned and antiferromagnetic in nature, dominate the intramolecular spin alignments in trinuclear and higher nuclearity mixed-valent complexes and often result in molecules that have large, and sometimes abnormally large, values of molecular spin ( S ). When coupled to a large molecular magnetoanisotropy of the easy-axis-type (negative zero-field splitting parameter, D ), also primarily resulting from individual Jahn–Teller distorted Mn III centres, such molecules will function as single-molecule magnets (molecular nanomagnets). Dissection of the structures and exchange interactions within a variety of mixed-valent Mn x cluster molecules with metal nuclearities of Mn 4 , Mn 12 and Mn 25 allows a ready rationalization of the observed S , D and overall magnetic properties in terms of competing antiferromagnetic exchange interactions within triangular subunits, resulting spin alignments and relative orientation of Mn III JT axes. Such an understanding has provided a stepping stone to the identification of a ‘magnetically soft’ Mn 25 cluster whose groundstate spin S value can be significantly altered by relatively minor structural perturbations. Such ‘spin tweaking’ has allowed this cluster to be obtained in three different forms with three different groundstate S values.