Jr. Kirchhoff et al., ELECTROCHEMISTRY AND SPECTROELECTROCHEMISTRY OF [RE(1,2-BIS(DIMETHYLPHOSPHINO)ETHANE)(3)](+), Inorganica Chimica Acta, 262(2), 1997, pp. 195-202
The electrochemical properties of [Re(dmpe)(3)](+), where dmpe is 1,2-
bis(dimethylphosphino)ethane, have been investigated in aqueous and no
n-aqueous solutions by cyclic and square wave voltammetry as well as b
y thin-layer electrochemical and spectroelectrochemical techniques. Th
e redox behavior in N,N-dimethylformamide (DMF) is described in terms
of three interrelated one-electron oxidations and the chemistry from d
ecomposition of electrogenerated Re(III) species. The first and third
redox processes are assigned to the oxidation of [Re(dmpe)(3)](+) to [
Re(dmpe)3](2+) and [Re(dmpe)(3)](2+) to [Re(dmpe)(3)](3+); the corresp
onding E-p values from square wave voltammetry are +0.336 and +1.120 V
versus Ag/AgCl (3 M NaCl). The second redox process (+0.884 V) is des
cribed as the oxidation of an Re(II) species, [Re(dmpe)(2)(eta(1)-dmpe
)S](2+) (S = a solvent molecule), which is proposed as an intermediate
in the dissociation of a dmpe ligand. Complete dissociation of dmpe o
ccurs from the Re(III) complexes to yield a species denoted as [Re(dmp
e)(2)S-2](3+), which is reduced with a peak potential from square wave
voltammetry at -0.288 V in DMF. Identification of this species as a b
is(dmpe) complex is accomplished by comparison of its FAB mass spectru
m UV-Vis spectrum, HPLC retention time, and electrochemical properties
to those of an independently synthesized complex, where S is replaced
by Cl-.