SOLUTION STUDIES OF THE REACTION BETWEEN THE PYRROLENINE ANION O-5-IMINO-2,5-DIHYDRO-1H-PYRROL-2-YLIDENE)ETHANIDE AND PALLADIUM(II) CHLORIDES - FORMATION AND CHARACTERIZATION OF THE MONO ETA-DIIMINO-TETRACYANO-PYRROLIZINIDO-PALLADIUM(II) COMPLEX
A. Flamini et N. Poli, SOLUTION STUDIES OF THE REACTION BETWEEN THE PYRROLENINE ANION O-5-IMINO-2,5-DIHYDRO-1H-PYRROL-2-YLIDENE)ETHANIDE AND PALLADIUM(II) CHLORIDES - FORMATION AND CHARACTERIZATION OF THE MONO ETA-DIIMINO-TETRACYANO-PYRROLIZINIDO-PALLADIUM(II) COMPLEX, Polyhedron, 15(3), 1996, pp. 513-518
The metal-assisted isomerization of the pyrrolenine anion o-5-imino-2,
5-dihydro-1H-pyrrol-2-ylidene)ethanide (C11N7H2-, L') to the 7-tetracy
ano-3,5-diimino-2,5-dihydro-pyrrolizinide anion (L) has been studied i
n solutions of CH2Cl2 or tetrahydrofuran (THF) with the palladium(II)
chlorides, PdCl42- or Pd2Cl62-, respectively. In THF the bis-chelate P
dL(2) and the mono-chelate PdLCl(2)(-) are formed. In CH2Cl2, only mon
o-chelate species are formed such as PdLCl(2)(-) or PdLCl(CN)(-). The
mono-chelate species show an optical spectrum, due to the drop PdL chr
omophore, qualitatively more similar to that of the corresponding phth
alocyanine, PdPc, than that of PdL(2).