Beckers Igor, Vos Christophe, Van Dessel Hendrik, Lauwers Aline, Stuyck Wouter, Usoltsev Oleg, Skorynina Alina, Bugaev Aram, De Vos Dirk
Department of Microbial and Molecular Systems, KULeuven, Celestijnenlaan 200F, 3001 Leuven, Belgium.
CELLS-ALBA Synchrotron Radiation Facility, Carrer de la Llum 2-26, 08290 Cerdanyola del Vallès, Spain.
ACS Catal. 2024 Apr 22;14(9):7080-7086. doi: 10.1021/acscatal.4c01699. eCollection 2024 May 3.
The Pd-catalyzed C-H activation of natural tryptophan residues has emerged as a promising approach for their direct synthetic modification. While using water as the solvent and harnessing air as the oxidant is enticing, these conditions induce catalyst deactivation by promoting the formation of inactive Pd(0) clusters. In this work, we have studied optimized Pd-based catalytic systems via nonsteady state kinetic analysis and X-ray absorption spectroscopy (XAS) to overcome catalyst deactivation, which enables the effective use of lower Pd loadings.
钯催化天然色氨酸残基的C-H活化已成为对其进行直接合成修饰的一种有前景的方法。虽然使用水作为溶剂并利用空气作为氧化剂很诱人,但这些条件会通过促进无活性Pd(0)簇的形成而导致催化剂失活。在这项工作中,我们通过非稳态动力学分析和X射线吸收光谱(XAS)研究了优化的钯基催化体系,以克服催化剂失活,从而能够有效使用较低的钯负载量。