These are preliminary reports that have not been peer-reviewed. They should not be regarded as conclusive, guide clinical practice/health-related behavior, or be reported in news media as established information. For more information, please see our FAQs.
4 files

PQQ-Aza-Crown Ether Complexes as Biomimetics for Lanthanide and Calcium Dependent Alcohol Dehydrogenases

submitted on 26.01.2021, 15:13 and posted on 28.01.2021, 09:23 by Violeta A. Vetsova, Katherine R. Fisher, Henning Lumpe, Alexander Schäfer, Erik K. Schneider, Patrick Weis, Lena Daumann
Understanding the role of metal ions in biology can lead to the development of new catalysts for
several industrially important transformations. Lanthanides are the most recent group of metal ions
that have been shown to be important in biology i.e. - in quinone-dependent methanol
dehydrogenases (MDH). Here we evaluate a pyrroloquinoline quinone and 1-aza-15-crown-5 based
ligand platform as scaffold for Ca2+ , Ba2+ , La3+ and Lu3+ biomimetics of MDH and we evaluate the
importance of ligand design, charge, size, counterions and base for the alcohol oxidation reaction
using NMR spectroscopy. In addition, we report a new straightforward synthetic route (3 steps
instead of 11 and 33% instead of 0.6% yield) for biomimetic ligands based on PQQ. We show that
when studying biomimetics for MDH, larger metal ions and those with lower charge in this case
promote the dehydrogenation reaction more effectively and that this is likely an effect of the ligand
design which must be considered when studying biomimetics. To gain more information on the
structures and impact of counterions of the complexes, we performed collision induced dissociation
(CID) experiments and observe that the nitrates are more tightly bound than the triflates. To resolve
the structure of the complexes in the gas phase we combined DFT-calculations and ion mobility
measurements (IMS). Furthermore, we characterized the obtained complexes and reaction mixtures
using Electron Paramagnetic Resonance (EPR) spectroscopy and show the emergence of a quinone-
based radical during the reaction with substrate and base.




Email Address of Submitting Author


Ludwig-Maximilians-Universität München



ORCID For Submitting Author


Declaration of Conflict of Interest

No Conflict of interest

Version Notes

First Version