74751-79-4

Upstream product

• 67-56-1 methanol 
• 917-23-7 5,10,15,20-tetraphenyl-21H,23H-porphine 
• 13939-06-5 molybdenum hexacarbonyl 
• 73515-84-1 {oxomolybdenum(V) tetraphenylporphyrine(NCS)} 
• 124-41-4 sodium methylate 
• 69063-76-9 Chloro-oxo(5,10,15,20-tetraphenylporphyrinato)molybdenum(V) 
• 73515-72-7 {oxomolybdenum(V) tetraphenylporphyrine(Br)} 

Downstream Products

• 102978-42-7 [oxomolybdenum(V)(tetraphenylporphyrin)(Me₂SO)](OCH₃) 
• 77320-98-0 oxo(acetato)molybdenum(V) tetraphenylporphyrin 
• 69063-76-9 Chloro-oxo(5,10,15,20-tetraphenylporphyrinato)molybdenum(V) 

Relevant academic research and scientific papers

Reversibility in the formation of oxo(peroxo)porphyrinatomolybdenums

Reversibility in the formation reaction of a series of the oxo(peroxo)porphyrinatomolybdenums, [Mo(VI)O(tmp)(O2)] 1, [Mo(VI)O(tdcpp)(O2)] 2, [Mo(VI)O(ttp)(O2)] 3, [Mo(VI)O(tdmpp)(O2)] 4, and [Mo(VI)O(tpp)(O2)] 5, was studied. In these dioxygen complexes with various porphyrin rings, two complexes, 2 and 4, were newly prepared by the solid- state reactions of corresponding Mo(IV) complexes with O2. All the complexes were characterized by IR, 1H NMR, and UV- vis spectroscopic measurements. In the reaction of O2 with [Mo(IV)O(tdcpp)] 2r, which has bulky substituents with an electron-withdrawal character, the association rate constant was determined to be 1.2 x 10-2 dm3 mol-1 s-1 in toluene at 20 °C. The value of the rate constant is about one thirtieth of that for [Mo(IV)O(tmp)] 1r, which also has bulky substituents. The result indicates that the electronic effects of the porphyrin rings, which reflect on the redox potentials of the central molybdenum ion, are important in determining kinetic and thermodynamic stability of the dioxygen complexes. All the dioxygen complexes undergo deoxygenation upon photoirradiation to give corresponding [Mo(IV)O(por)]. The redioxy-genation profiles of [Mo(IV)O(por)] in the dark were also significantly affected by the steric bulkiness of the porphyrin ligands. While the bulky porphyrin complexes of 1 and 2 gave full recovery of the dioxygen complexes in the dark, less bulky porphyrin complexes of 3, 4, and 5 undergo some side reactions to Mo(V) species. The rate and extent of the Mo(V) complex formations increase with decreasing steric bulkiness.

MECHANISM OF THE REACTIONS OF OXOMOLYBDENUM(V) TETRAPHENYLPORPHYRIN COMPLEX WITH ALCOHOLS IN THE PRESENCE OF SUPEROXIDE.

The successive addition of ROH (R equals CH//3 and C//2H//5) to the dichloromethane solution of Mo**vO(tpp)Br (tpp equals meso-tetraphenylporphinato) causes two-step reactions at 25 degree C. The products of the first and the second step of the reactions are alcohol complex, left bracket Mo**vO(tpp)(ROH) right bracket Br, and alkoxo complex, Mo**vO(tpp)OR, respectively. In the presence of superoxide ion, O//2** minus , in the dichloromethane solution of Mo**vO(tpp)X (X equals Br and NCS) containing alcohol, Mo**vO(tpp)OR is formed through competitive two reaction paths where O//2** minus acts as a proton acceptor and a reducing agent. The reaction steps of the two paths were confirmed by optical and ESR studies.