A MnIIMnIII‐Peroxide Complex Capable of Aldehyde Deformylation. (27th March 2019)

• Record Type: Journal Article
• Authors: Magherusan, Adriana M.; Kal, Subhasree; Nelis, Daniel N.; Doyle, Lorna M.; Farquhar, Erik R.; Que, Lawrence; McDonald, Aidan R.
• Is Part Of: Angewandte Chemie. Volume 131:Number 17(2019)
• Page Start: 5774
• Page End: 5778
• Publication Date: 2019-03-27
• Subjects: Aldehyd-Deformylierung -- MnIIMnIII-Peroxide -- Nukleophile Reaktivität -- Ribonukleotidreduktasen -- Superoxid-Aktivierung; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201900717
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Ribonucleotide reductases (RNRs) are essential enzymes required for DNA synthesis. In class Ib Mn2 RNRs superoxide (O2 .− ) was postulated to react with the Mn II 2 core to yield a Mn II Mn III ‐peroxide moiety. The reactivity of complex1 ([Mn II 2 (O2 CCH3 )2 (BPMP)](ClO4 ), where HBPMP=2, 6‐bis{[(bis(2‐pyridylmethyl)amino]methyl}‐4‐methylphenol) towards O2 .− was investigated at −90 °C, generating a metastable species, 2 . The electronic absorption spectrum of2 displayed features ( λ max =440, 590 nm) characteristic of a Mn II Mn III ‐peroxide species, representing just the second example of such. Electron paramagnetic resonance and X‐ray absorption spectroscopies, and mass spectrometry supported the formulation of2 as a Mn II Mn III ‐peroxide complex. Unlike all other previously reported Mn2 ‐peroxides, which were unreactive, 2 proved to be a capable oxidant in aldehyde deformylation. Our studies provide insight into the mechanism of O2 ‐activation in Class Ib Mn2 RNRs, and the highly reactive intermediates in their catalytic cycle.