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

Authors
Citation
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
Citations number
8
Categorie Soggetti
Chemistry Inorganic & Nuclear",Crystallography
Journal title
ISSN journal
02775387
Volume
15
Issue
3
Year of publication
1996
Pages
513 - 518
Database
ISI
SICI code
0277-5387(1996)15:3<513:SSOTRB>2.0.ZU;2-T
Abstract
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).