5,5‘-Bridged Bis(1,2,3-dithiazoles): Spin States and Charge-Transfer Chemistry

Bifunctional 1,2,3-dithiazoles bridged with azine and phenylenediamine spacers have been prepared, with a view
to determining the extent of communication between the two dithiazole rings as a function of the electronic and
steric demands of the bridge. The crystal structure of the closed-shell diazine derivative [S2NClC2NNC2ClNS2] is rigorously planar. Cyclic voltammetry on this compound indicates two reversible one-electron oxidations.
The radical cation state has been characterized by EPR spectroscopy and by crystal structure determination of its
1:1 PF6- salt. The latter reveals little interaction between neighboring radical cations; consistently, the material
exhibits a conductivity of σ < 10-5 S cm-1. Insertion of a phenylene group into the diazine bridge to afford
[S2NClC2NC6H4NC2ClNS2] leads to significant torsional motion between the phenylene ring and the two end
groups, as a result of which the two DTA rings are electronically independent; no radical cation state has been
observed for this species. Crystal data for Cl2S4N4C4: a = 5.1469(15), b = 13.343(2), c = 14.2031(17),
orthorhombic, Pbca, Z = 4. Crystal data for Cl2S4N4C4PF6: a = 11.699(4), b = 12.753(5), c = 10.461(4),
β = 112.17(1)°, monoclinic, C2/c, Z = 4. Crystal data for Cl2S4N4C10H4: a = 3.9477(6), b = 23.790(3),
c = 7.3769(9), β =90.793(12)°, monoclinic, P21/c, Z = 2.