TY - JOUR
T1 - A Co(III)-peroxo-arylboronate complex formed by nucleophilic reaction of a Co(III)-peroxo species
AU - Li, Yan
AU - Handunneththige, Suhashini
AU - He, Wenting
AU - Talipov, Marat R.
AU - Wang, Dong
N1 - Copyright © 2024 Elsevier Inc. All rights reserved.
PY - 2024/7
Y1 - 2024/7
N2 - In this work, we report the generation and characterization of two new Co(III)-peroxo complexes 2 and 3. 2 is best described as a mononuclear CoIII-(O2) complex that exhibits an 18O-isotope sensitive O–O bond stretching vibration at 845(−49) cm−1, indicating a relatively weak peroxo moiety compared to those of other CoIII-(O2) complexes reported previously. Complex 3 is a CoIII-peroxo-arylboronate species having a rare {CoIIIOOBO} five-membered metallocycle, which is structurally characterized using X-ray crystallography. Investigations of the reaction mechanism using density functional theory calculations show that 2 likely undergoes a nucleophilic attack to an arylboronic acid, which is generated by hydrolysis of the BPh4− anion in wet acetonitrile solution, to first form a CoIII-peroxo-arylboronic acid adduct, followed by the loss of one benzene molecule to generate the five-membered metallocycle. The entire reaction is thermodynamically favorable. Taken together, the conversion of 2 to 3 represents the discovery of a novel nucleophilic reactivity that can be carried out by mononuclear Co(III)-peroxo complexes.
AB - In this work, we report the generation and characterization of two new Co(III)-peroxo complexes 2 and 3. 2 is best described as a mononuclear CoIII-(O2) complex that exhibits an 18O-isotope sensitive O–O bond stretching vibration at 845(−49) cm−1, indicating a relatively weak peroxo moiety compared to those of other CoIII-(O2) complexes reported previously. Complex 3 is a CoIII-peroxo-arylboronate species having a rare {CoIIIOOBO} five-membered metallocycle, which is structurally characterized using X-ray crystallography. Investigations of the reaction mechanism using density functional theory calculations show that 2 likely undergoes a nucleophilic attack to an arylboronic acid, which is generated by hydrolysis of the BPh4− anion in wet acetonitrile solution, to first form a CoIII-peroxo-arylboronic acid adduct, followed by the loss of one benzene molecule to generate the five-membered metallocycle. The entire reaction is thermodynamically favorable. Taken together, the conversion of 2 to 3 represents the discovery of a novel nucleophilic reactivity that can be carried out by mononuclear Co(III)-peroxo complexes.
KW - Cobalt-peroxo-arylboronate species
KW - Five-membered metallocycle
KW - Mononuclear metal-peroxo species
KW - Nucleophilic reaction
KW - Side-on cobalt-peroxo complex
KW - Cobalt/chemistry
KW - Boronic Acids/chemistry
KW - Crystallography, X-Ray
KW - Molecular Structure
KW - Coordination Complexes/chemistry
UR - http://www.scopus.com/inward/record.url?scp=85190156722&partnerID=8YFLogxK
U2 - 10.1016/j.jinorgbio.2024.112552
DO - 10.1016/j.jinorgbio.2024.112552
M3 - Article
C2 - 38608554
AN - SCOPUS:85190156722
SN - 0162-0134
VL - 256
SP - 112552
JO - Journal of Inorganic Biochemistry
JF - Journal of Inorganic Biochemistry
M1 - 112552
ER -