PHENYLLEAD(IV) DIORGANOPHOSPHINODITHIOATES, PH(N)PB(S(2)PR(2))(4-N) -SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION, AND NMR-STUDY OF THE REDISTRIBUTION DECOMPOSITION OF DIPHENYLLEAD(IV) DERIVATIVES
C. Silvestru et al., PHENYLLEAD(IV) DIORGANOPHOSPHINODITHIOATES, PH(N)PB(S(2)PR(2))(4-N) -SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION, AND NMR-STUDY OF THE REDISTRIBUTION DECOMPOSITION OF DIPHENYLLEAD(IV) DERIVATIVES, Heteroatom chemistry, 5(4), 1994, pp. 327-336
Tri- and diphenyllead(IV) diorganophosphinodithioates, Ph(n)Pb(S(2)PR(
2))(4-n) (n = 2 and 3; R = Me, Et, Ph) were prepared by reacting the c
orresponding organolead(IV) chloride with the sodium or ammonium salt
of the phosphinodithioic acid. The title compounds were investigated b
y infrared, H-1 and P-31 NMR, and mass spectroscopy, and possible stru
ctures were proposed. The diphenyllead(IV) phosphinodithioates, Ph(2)P
b(S(2)PR(2))(2), undergo decomposition on standing or on moderate heat
ing, the least stable being the ethyl derivative. The process was moni
tored by using H-1 and P-31 NMR spectroscopy, and a reaction pathway l
eading to Ph(3)PbS(2)PR(2), Pb(S(2)PR(2))2, and R(2)P(S)SPh was establ
ished.