Carbonyl complexes, chromium cobalt-platinum

FT-ICR, see Fourier-transform ion cyclotron resonance Fullerene[60], germanium-germanium addition, 10, 748 Fullerenes with cobalt, 7, 51 on cobalt Cp rings, 7, 73 inside metallodendrimers, 12, 401 microwave applications, 1, 334 Pd rc-complexes, 8, 348 Ru—Os complexes, 6, 830 with tungsten carbonyls, 5, 687 )2-Fullerenes, with platinum, 8, 634 Fulvalene actinide complex, synthesis, 4, 232 Fulvalene chromium carbonyls, synthesis and characteristics, 5, 264... 

Vanhoye and coworkers [402] synthesized aldehydes by using the electrogenerated radical anion of iron pentacarbonyl to reduce iodoethane and benzyl bromide in the presence of carbon monoxide. Esters can be prepared catalytically from alkyl halides and alcohols in the presence of iron pentacarbonyl [403]. Yoshida and coworkers reduced mixtures of organic halides and iron pentacarbonyl and then introduced an electrophile to obtain carbonyl compounds [404] and converted alkyl halides into aldehydes by using iron pentacarbonyl as a catalyst [405,406]. Finally, a review by Torii [407] provides references to additional papers that deal with catalytic processes involving complexes of nickel, cobalt, iron, palladium, rhodium, platinum, chromium, molybdenum, tungsten, manganese, rhenium, tin, lead, zinc, mercury, and titanium. 

Tin(II) bis(jS-ketonolates), Sn[0CRCHCR (=0)]2 (R, R = Me, CFj, Ph), are also excellent donor molecules to transition metal carbonyl residues, readily forming the type D structure chromium, molybdemun and tungsten complexes (8) under photolysis in tetrahydrofuran, as well as the manganese complexes (9). The cobalt complexes (10) and (11) prepared by the same method are somewhat different, and in these the stannylene functions as a bridging group. The two platinum(0) complexes (12) and (13) have been obtained from the reaction of tin(II) bis(pentane-2,4-dionate) and Pt(C2H4)(PPhj)2 under different conditions. ... 

---