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Paramagnetic organoiron intermediates. Final report

Technical Report ·
OSTI ID:5835297

The neutral carbonyl compounds of iron, Fe(CO)/sub 5/, Fe/sub 2/(CO)/sub 9/, Fe/sub 3/(CO)/sub 12/, and the related carbonylate dianions, Fe(CO)/sub 4//sup 2 -/, Fe/sub 2/(CO)/sub 8//sup 2 -/, Fe/sub 3/(CO)/sub 11//sup 2 -/, Fe/sub 4/(CO)/sub 13//sup 2 -/, and their conjugate acids, HFe(CO)/sub 4//sup -/, HFe/sub 2/(CO)/sub 8//sup -/, HFe/sub 3/(CO)/sub 11//sup -/, HFe/sub 4/(CO)/sub 13//sup -/, occupy an important position in organometallic chemistry. Several of these reagents are employed as useful stoichiometric reagents or precursors to catalytically active species. They are all diamagnetic and their very considerable chemistry has been discussed virtually exclusively in terms of even-electron mechanisms. Our studies, however, have revealed a new series of iron carbonyl species which parallels the carbonylate dianions and are related to the latter by having one less electron. The existence of these radical anions, their conjugate protonated species (vide infra), and other organoiron radicals (vide infra) suggests an important but not yet generally recognized role for one-electron pathways in the chemistry of iron carbonyl compounds.

Research Organization:
Rutgers--the State Univ., New Brunswick, NJ (USA)
DOE Contract Number:
AS05-80ER10662
OSTI ID:
5835297
Report Number(s):
DOE/ER/10662-T1; ON: DE85009471
Country of Publication:
United States
Language:
English