Search results
Results from the WOW.Com Content Network
Molybdenum hexacarbonyl is a popular reagent in academic research. [6]One or more CO ligands can be displaced by other ligands. [7] Mo(CO) 6, [Mo(CO) 3 (MeCN) 3], and related derivatives are employed as catalysts in organic synthesis for example, alkyne metathesis and the Pauson–Khand reaction.
Mo(CO) 6 reacts with arenes to give piano-stool complexes such as (mesitylene)molybdenum tricarbonyl. Cycloheptatrienemolybdenum tricarbonyl, which is related to (arene)Mo(CO) 3, reacts with trityl salts to give the cycloheptatrienyl complex: [3] (C 7 H 8)Mo(CO) 3 + (C 6 H 5) 3 C + → [(C 7 H 7)Mo(CO) 3] + + (C 6 H 5) 3 CH Structure of ...
The six CO ligands are terminal and the Mo-Mo bond distance is 3.2325 Å. [2] The compound is prepared by treatment of molybdenum hexacarbonyl with sodium cyclopentadienide followed by oxidation of the resulting NaMo(CO) 3 (C 5 H 5). [3] Other methods have been developed starting with Mo(CO) 3 (CH 3 CN) 3 instead of Mo(CO) 6. [4]
(Mesitylene)molybdenum tricarbonyl arises from the reaction of molybdenum hexacarbonyl with hot mesitylene: [1]. Mo(CO) 6 + (CH 3) 3 C 6 H 3 → Mo(CO) 3 [(CH 3) 3 C 6 H 3] + 3 CO It can also be synthesized, with good yields by displacement of pyridine ligands of the trispyridine complex Mo(CO) 3 (pyridine) 3 in the presence of Lewis acids.
The dark-blue phosphorus-containing heteropolymolybdate P[Mo 12 O 40] 3− is used for the spectroscopic detection of phosphorus. [31] The broad range of oxidation states of molybdenum is reflected in various molybdenum chlorides: [26] Molybdenum(II) chloride MoCl 2, which exists as the hexamer Mo 6 Cl 12 and the related dianion [Mo 6 Cl 14] 2-.
C 7 H 8 + Mo(CO) 6 → (C 7 H 8)Mo(CO) 3 + 3 CO. The compound is a piano stool complex, consisting of Mo(CO) 3 bound to six carbon centers of the triene. The methylene group projects from the plane of the six coordinated carbon atoms. [3] The compound reacts with trityl salts to give the cycloheptatrienyl complex: [4]
W(CO) 6 behaves similarly to the Mo(CO) 6 but tends to form compounds that are kinetically more robust. Cyclopentadienyltungsten tricarbonyl dimer ((C 5 H 5.) 2 W 2 (CO) 6) is produced from W(CO) 6. Treatment of tungsten hexacarbonyl with sodium cyclopentadienide followed by oxidation of the resulting NaW(CO) 3 (C 5 H 5) gives ...
2 Mo(CO) 6 + 4 HO 2 CCH 3 → Mo 2 (O 2 CCH 3) 4 + 12 CO + 2 H 2. Trinuclear clusters are byproducts. [7] The reaction of HO 2 CCH 3 and Mo(CO) 6 was first investigated by Bannister et al. in 1960. At the time, quadruple metal-metal bonds had not yet been discovered, so these authors proposed that Mo(O 2 CCH 3) 2 was tetrahedral.