TY - JOUR
T1 - Role of decomposition products in the oxidation of cyclohexene using a manganese(III) complex
AU - Zand, Zahra
AU - Mousazade, Younes
AU - Arevalo, Ryan Lacdao
AU - Bagheri, Robabeh
AU - Mohammadi, Mohammad Reza
AU - Bikas, Rahman
AU - Chernev, Petko
AU - Aleshkevych, Pavlo
AU - Vandichel, Matthias
AU - Song, Zhenlun
AU - Dau, Holger
AU - Najafpour, Mohammad Mahdi
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Metal complexes are extensively explored as catalysts for oxidation reactions; molecular-based mechanisms are usually proposed for such reactions. However, the roles of the decomposition products of these materials in the catalytic process have yet to be considered for these reactions. Herein, the cyclohexene oxidation in the presence of manganese(III) 5,10,15,20-tetra(4-pyridyl)-21H,23H-porphine chloride tetrakis(methochloride) (1) in a heterogeneous system via loading the complex on an SBA-15 substrate is performed as a study case. A molecular-based mechanism is usually suggested for such a metal complex. Herein, 1 was selected and investigated under the oxidation reaction by iodosylbenzene or (diacetoxyiodo)benzene (PhI(OAc)2). In addition to 1, at least one of the decomposition products of 1 formed during the oxidation reaction could be considered a candidate to catalyze the reaction. First-principles calculations show that Mn dissolution is energetically feasible in the presence of iodosylbenzene and trace amounts of water.
AB - Metal complexes are extensively explored as catalysts for oxidation reactions; molecular-based mechanisms are usually proposed for such reactions. However, the roles of the decomposition products of these materials in the catalytic process have yet to be considered for these reactions. Herein, the cyclohexene oxidation in the presence of manganese(III) 5,10,15,20-tetra(4-pyridyl)-21H,23H-porphine chloride tetrakis(methochloride) (1) in a heterogeneous system via loading the complex on an SBA-15 substrate is performed as a study case. A molecular-based mechanism is usually suggested for such a metal complex. Herein, 1 was selected and investigated under the oxidation reaction by iodosylbenzene or (diacetoxyiodo)benzene (PhI(OAc)2). In addition to 1, at least one of the decomposition products of 1 formed during the oxidation reaction could be considered a candidate to catalyze the reaction. First-principles calculations show that Mn dissolution is energetically feasible in the presence of iodosylbenzene and trace amounts of water.
UR - http://www.scopus.com/inward/record.url?scp=85159656564&partnerID=8YFLogxK
U2 - 10.1038/s42004-023-00881-x
DO - 10.1038/s42004-023-00881-x
M3 - Article
AN - SCOPUS:85159656564
SN - 2399-3669
VL - 6
SP - 94
JO - Communications Chemistry
JF - Communications Chemistry
IS - 1
M1 - 94
ER -