78833-68-8Relevant articles and documents
Mechanistic studies of the oxidative cleavage of the molybdenum-mercury bonds in [CpMo(CO)2(PPh3)]2Hg
Lin, Chen C.,Gipson, Stephen L.
, p. 167 - 172 (2008/10/08)
Chemical or electrochemical oxidation of the trimetallic complex [CpMo(CO)2(PPh3)]2Hg (Cp = η5-C5H5) occurs in two one-electron steps. The first electron transfer generates a transient cation which undergoes Mo-Hg bond cleavage to generate a 16-electron species, [CpMo(CO)2(PPh3)]+, and a mercury-centered radical, CpMo(CO)2(PPh3)Hg?. To account for the products, it is proposed that the radical dimerizes and then reacts with half of the available 16-electron cation to form an observable pentametallic intermediate. The second electron transfer generates [CpMo(CO)2(PPh3)Hg]+ and returns the 0.5 mol of [CpMo(CO)2(PPh3)]+ which was incorporated into the intermediate. The mercury-containing cation subsequently eliminates metallic mercury to yield a second mole of [CpMo(CO)2(PPh3)]+. The 16-electron cation coordinates solvent or other available neutral or anionic ligands to yield 18-electron complexes.
METALLORGANISCHE LEWIS-SAEUREN; METALLKOMPLEXE MIT SCHWACH KOORDINIERTEN LIGANDEN. VIII. REAKTIONEN VON TETRAFLUOROBORATO-KOMPLEXEN (η5-C5H5)(CO)2(L)(MoFBF3 (L = CO, PR3) MIT ALKINEN
Suenkel, Karlheinz,Nagel, Ulrich,Beck, Wolfgang
, p. 251 - 262 (2007/10/02)
The reaction of the tetrafluoroborato compounds (η5-C5H5)(CO)2(L)MoFBF3 with various alkynes gives mono- and bis-alkyne complexes 5-C5H5)Mo(CO)(RCCR')2>+ BF4- (III) and 5-C5H5)Mo(CO)(L)(RCCR')>