Structural, Magnetic and DFT studies on a Charge-Transfer Salt of a Tetrathiafulvalenepyridyl-(1,5-diisopropyl) verdazyl Diradical Cation.

A new tetrathiafulvalene (TTF) donor covalently appended with a 1,5-diisopropylverdazyl radical through a cross-conjugated pyridyl linker ( 3) has been prepared and characterised. Reaction of 3 with tetracyanoquinonedimethane (TCNQ) afforded the 2:1 charge-transfer complex ( 3)₂ ⋅TCNQ ( 4), in which the IR and structural data are consistent with 0.25 e⁻ charge transfer from the TTF donor (D) to the TCNQ acceptor (A). The TTF and TCNQ molecules adopt a mixed-stack D⋅⋅⋅D⋅⋅⋅A arrangement that does not facilitate conduction. A solution EPR spectrum of 4 comprises a broad featureless singlet, which is consistent with the presence of a TCNQ radical anion. Theoretical studies were performed to probe the exchange interactions within selected fragments of 4 with and without charge transfer. In the absence of charge transfer, DFT calculations reveal weak antiferromagnetic exchange between verdazyl radicals within the ( 3)₂ monoradical unit. However, partial oxidation of the dimer ( 3)₂ to the diradical cation leads to an S= [ABSTRACT FROM AUTHOR]