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Mimicking the Cu Active Site of Lytic Polysaccharide Monooxygenase Using Monoanionic Tridentate N-Donor Ligands.

Caitlin J BoucheyDimitar Y ShopovAaron D GruenWilliam B Tolman
Published in: ACS omega (2022)
In an effort to prepare small molecule mimics of the active site of lytic polysaccharide monooxygenase (LPMO), three monoanionic tridentate N donor ligands comprising a central deprotonated amide group flanked by two neutral donors were prepared, and their coordination chemistry with Cu(I) and Cu(II) was evaluated. With Cu(I), a dimer formed, which was characterized by X-ray crystallography and NMR spectroscopy. A variety of mononuclear and dinuclear Cu(II) species with a range of auxiliary ligands (MeCN, Cl - , OH - , OAc - , OBz - , CO 3 2- ) were prepared and characterized by X-ray diffraction and various spectroscopies (UV-vis, EPR). The complexes exhibit structural similarities to the LPMO active site.
Keyphrases
  • aqueous solution
  • small molecule
  • metal organic framework
  • high resolution
  • mass spectrometry
  • magnetic resonance imaging
  • electron microscopy
  • protein protein
  • drug discovery