Synthesis, electrochemical investigation and EPR spectroscopy of a reversible four-stage redox system based on mesoionic 5,5 '-azinobis(1,3-diphenyltetrazole) and related mesoionic compounds
S. Araki et al., Synthesis, electrochemical investigation and EPR spectroscopy of a reversible four-stage redox system based on mesoionic 5,5 '-azinobis(1,3-diphenyltetrazole) and related mesoionic compounds, J CHEM S P2, (5), 1999, pp. 985-995
Citations number
20
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
Mesoionic 5,5'-azinobis(1,3-diphenyltetrazole) 1 was prepared, and its chem
ical oxidation gave stable crystals of the corresponding radical cation 1(.
+) and dication 1(2+),which reversibly gave back azine 1 on reduction with
zinc. Electrochemical investigations of 1 using cyclovoltammetry and differ
ential pulse voltammetry in pyridine (Py) or dichloromethane (DCM) also rev
ealed the two reversible successive one-electron oxidations leading to dica
tion 1(2+) via radical cation 1(.+), both of which can be reduced to the ne
utral state 1. In the cathodic process, 1 was reduced by two consecutive on
e-electron transfers at only slightly different potentials up to the corres
ponding dianion 1(2-) which could be re-oxidized to the neutral state; thus
constituting a reversible four-stage redox system. Radical cation 1(.+) an
d anion 1(.-) were characterized by EPR spectroscopy. In order to get more
insights into the spin-density distribution of 1(.+), the bis- and tetra-N-
15-labelled species 1a(.+), 1b(.+) and 1c(.+) were synthesized and investig
ated by EPR and N-15 as well as N-14 ENDOR spectroscopy, revealing ti;at th
e largest N hyperfine coupling constants are due tb the nitrogen atoms of t
he central bridge. According to H-1 ENDOR there seems to be a small couplin
g with the protons of both phenyl rings which cannot be resolved in the EPR
spectrum.
The electrochemical properties of the related mesoionic compounds 5-10 were
also investigated in Py or DCM solutions. In the cathodic process, a reduc
tion peak of 9 and 10 was observed due to their reversible one-electron red
uction to the corresponding radical anions. The radical obtained on reducti
on of 10 was characterized by EPR spectroscopy. On the other hand, 5-8 can
be reduced by a formal two-electron transfer up to the corresponding dianio
ns which are re-oxidizable to the neutral state. In the anodic process, 9/1
0 undergo irreversible one-electron oxidations whereas 5/6 (in DCM) and 7/8
(in Py) experience reversible or irreversible step by step two-electron ox
idations leading to the dications. In By the oxidation products of 5/6 reac
t to further species revealing two more oxidation and several rereduction p
eaks. On the other hand, the oxidation products of 7/8 are instable in DCM
(one main oxidation and rereduction peak). The electrochemical data are dis
cussed in terms of delocalization in the cations and conjugation in the dic
ations.