Year: 2025
Type: article
Abstract: Sustainable catalysts based on main-group elements, such as frustrated Lewis pairs (FLPs), have emerged as alternatives to precious metal systems. The initial reaction of the Lewis acid, Lewis base and small molecule ( e.g . H 2 ) is formally termolecular, but the reaction is rationalised by the pre-association of the acid and base in an encounter complex. Here we show that the charge-transfer band between P(mes) 3 and B(C 6 F 5 ) 3 can be analysed by supramolecular UV-vis spectroscopic techniques to provide the key thermodynamic parameter, the association constant ( K a ), for the active encounter complex, i.e . the pre-associated complex that is specifically in the correct orientation for small-molecule activation. We also demonstrate that a higher concentration of active encounter complex in solution leads to a faster activation of hydrogen. This method enables researchers to directly probe the complex that underpins FLP small-molecule activation and subsequent catalysis, and will aid the design of more active sustainable catalysts.
Source: Nature Communications
Institutions: University of Birmingham, University of Liverpool
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $6,990
OpenAlex ID: W4409530213