Publisher: Wiley

Issue: 21

License: http://creativecommons.org/licenses/by/4.0/

Publication date(s): 2019/11/07 (print) 2019/09/06 (online)

Pages: 5313-5321

Volume: 11 Issue: 21

Journal: ChemCatChem

Link: https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fcctc.201901268

URL: http://dx.doi.org/10.1002/cctc.201901268

Real-time Small Angle X-Ray Scattering (SAXS) has been used to investigate the homogeneity of a series of molecular iridium complexes during water oxidation catalysis in aqueous NaIO₄ solution through a continuous flow cell. The results obtained for the unstable [Cp*Ir(OH₂)₃]²⁺ precursor forming amorphous IrO_x nanoparticles (NPs) in-situ validate and complement previous Dynamic Light Scattering (DLS) studies by providing enhanced sensitivity for small particle sizes and increased temporal resolution under realistic reaction conditions. Correlating particle formation profiles with O₂ evolution traces allowed homogeneous catalysis to be clearly distinguished from heterogeneous catalysis. A series of seven pyridine−alkoxide Cp*Ir complexes are shown to be fully homogeneous by SAXS, validating previous studies and confirming their catalysis to be molecular in nature throughout the reaction.