SYNTHESIS AND SPECTROSCOPIC STUDIES OF PENTACARBONYLFUMARONITRILE-CHROMIUM(0), PENTACARBONYLFUMARONITRILE-MOLYBDENUM(0), AND PENTACARBONYLFUMARONITRILE-TUNGSTEN(0)

1994-08-01
MOUR, IA
Özkar, Saim
KREITER, CG
Photolysis of hexacarbonyl-chromium(0), -molybdenum(0), and -tungsten(0) in presence of fumaronitrile yields at room temperature pentacarbonyl-fumaronitrile-chromium(0) (1): molybdenum(0) (2), and -tungsten(0) (3). The complexes were purified by crystallization and characterized by IR and C-13-NMR spectroscopy. The fumaronitrile ligand is bonded to the M(CO)(5) moiety by one nitrile nitrogen atom rather than by the carbon-carbon double bond. In toluene 2 dissociates into fumaronitrile and pentacarbonyl-molybdenum(0), which is stabilized by the solvent. Fumaronitrile and solvated pentacarbonyl-molybdenum(0) exist in solution together with 2 in an equilibrium which lies in favour of the former species.
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES

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Citation Formats
I. MOUR, S. Özkar, and C. KREITER, “SYNTHESIS AND SPECTROSCOPIC STUDIES OF PENTACARBONYLFUMARONITRILE-CHROMIUM(0), PENTACARBONYLFUMARONITRILE-MOLYBDENUM(0), AND PENTACARBONYLFUMARONITRILE-TUNGSTEN(0),” ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, pp. 1059–1062, 1994, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/52575.