Charge-Localizedp-Phenylenedihydrazine Radical Cations: ESR and Optical Studies of Intramolecular Electron Transfer Rates

1,4-Bis(2-tert-butyl-2,3-diazabicyclo[2.2.2]oct-3-yl)benzene-1,4-diyl (2) its 2,5-dimethyl and 2,3,5,6-tetramethyl derivatives (3 and 4), their radical cations, and bis-radical dications are studied. Crystal structures including those of 2+BPh4-, 32+(BPh4-)2, 4+BPh4-, and 42+(BPh4-)2 establish that ring methylation causes more N-lone pair, aryl π twist without changing the NAr,NAr distance significantly and that both 2+ and 4+ have the charge localized in one hydrazine unit. NMR measurements show that 3+ has about 6% of its spin at the four aryl CH and CMe carbons, while 4+ has about 1.5% of its spin at the four CMe carbons. The average distance between the unpaired electrons of 32+ and 42+ was obtained from the dipolar splittings of their thermally excited triplet states and, as expected, is significantly smaller for 32+ (5.25 Å) than for 42+ (5.63 Å). Rate constants for electron transfer between the hydrazine units of 3+ and 4+ in CH2Cl2 and CH3CN were determined by dynamic ESR. The intervalence radical cations show charge transfer bands corresponding to vertical electron transfer between the ground state and the highly vibrationally excited electron-shifted state, allowing calculation of the parameters controlling electron transfer. Electron transfer parameters obtained from the CT bands using adiabatic energy surfaces which approximate the CT band shapes observed produce rate constants within experimental error of those extrapolated to room temperature from the ESR data for both 3+ and 4+ in both solvents, without using tunneling corrections. The effects of mixing of the electronic wave functions of the reduced and oxidized hydrazine units of 2+ on dNN, the C(t-Bu)N,NA(Ar) twist angle, and the aryl nitrogen lone pair, aryl π twist angle which are observed by X-ray are close to those predicted from the position of the minima on the ET coordinate X of the adiabatic energy surface calculated from the CT band.