Rules for Magnetic Exchange in Azulene-Bridged Biradicals: Quo Vadis?

Abstract

Electronic coupling through organic bridges facilitates magnetic exchange interactions and controls electron transfer and single-molecule device electron transport. Electronic coupling through alternant π-systems (e.g., benzene) is better understood than the corresponding coupling through nonalternant π-systems (e.g., azulene). Herein, we examine the structure, spectroscopy, and magnetic exchange coupling in two biradicals (1,3-SQ2Az and 1,3-SQ-Az-NN; SQ = the zinc(II) complex of spin-1/2 semiquinone radical anion, NN = spin-1/2 nitronylnitroxide; Az = azulene) that possess nonalternant azulene π-system bridges. The SQ radical spin density in both molecules is delocalized into the Az π-system, while the NN spin is effectively localized onto the five-atom ONCNO π-system of NN radical. The spin distributions and interactions are probed by EPR spectroscopy and magnetic susceptibility measurements. We find that J = +38 cm-1 for 1,3-SQ2Az and J = +9 cm-1 for 1,3-SQ-Az-NN (H=-2JS^SQ·S^SQorNN). Our results highlight the differences in exchange coupling mediated by azulene compared to exchange coupling mediated by alternant π-systems.