TY - JOUR
T1 - O-O Bond activation in H2O2 and (CH3)3C-OOH mediated by [Ni(cyclam)(CH3CN)2] (ClO4)2: Different mechanisms to form the same Ni(iii) product?
AU - Solans-Monfort, Xavier
AU - Fierro, José Luis G.
AU - Hermosilla, Laura
AU - Sieiro, Carlos
AU - Sodupe, Mariona
AU - Mas-Ballesté, Rubén
PY - 2011/7/14
Y1 - 2011/7/14
N2 - Reaction of [NiII(cyclam)(CH3CN)2] (ClO4)2(1) with tert-butylhydroperoxide (TBHP) or H2O2, in acidic media results in a formation of [NiIII(cyclam)(CH3CN)2]3+species (2), the nature of which is characterized by UV-vis, EPR and XPS. The formation rate of 2 is much higher when H2O2is used as oxidant. In absence of acid, TBHP reacts with 1 generating the same Ni(iii) species but, in contrast, no reaction is observed between H2O2and 1. Addition of cis-stilbene as an oxidable substrate quenches the formation of Ni(iii) for reaction with H2O2only. Overall, these observations reveal a different reaction mechanism when reacting H2O2with 1 than when reacting the same metal complex with TBHP, despite the fact that the final product is the same. The proposed pathways arising from these observations consist in a homolytic O-O cleavage for the reaction of 1 with TBHP in CH3CN, but a proton assisted heterolysis for the O-O activation in H2O2. Density functional calculations (B3LYP and OPBE) on the thermodynamic feasibility of the two reaction processes support the proposed mechanisms, since the O-O homolysis is strongly disfavored when H2O2is used as reactant. © 2011 The Royal Society of Chemistry.
AB - Reaction of [NiII(cyclam)(CH3CN)2] (ClO4)2(1) with tert-butylhydroperoxide (TBHP) or H2O2, in acidic media results in a formation of [NiIII(cyclam)(CH3CN)2]3+species (2), the nature of which is characterized by UV-vis, EPR and XPS. The formation rate of 2 is much higher when H2O2is used as oxidant. In absence of acid, TBHP reacts with 1 generating the same Ni(iii) species but, in contrast, no reaction is observed between H2O2and 1. Addition of cis-stilbene as an oxidable substrate quenches the formation of Ni(iii) for reaction with H2O2only. Overall, these observations reveal a different reaction mechanism when reacting H2O2with 1 than when reacting the same metal complex with TBHP, despite the fact that the final product is the same. The proposed pathways arising from these observations consist in a homolytic O-O cleavage for the reaction of 1 with TBHP in CH3CN, but a proton assisted heterolysis for the O-O activation in H2O2. Density functional calculations (B3LYP and OPBE) on the thermodynamic feasibility of the two reaction processes support the proposed mechanisms, since the O-O homolysis is strongly disfavored when H2O2is used as reactant. © 2011 The Royal Society of Chemistry.
U2 - 10.1039/c0dt01605e
DO - 10.1039/c0dt01605e
M3 - Article
SN - 1477-9226
VL - 40
SP - 6868
EP - 6876
JO - Dalton Transactions
JF - Dalton Transactions
IS - 26
ER -