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Updated: Oct 3, 2025

Preparation and Use of Carbonyl-decorated Carbenes in the Activation of White Phosphorus
Published on: October 3, 2014
Factors Governing the Catalytic Insertion of CO2 into Arenes - A DFT Case Study for Pd and Pt Phosphane Sulfonamido
Markus Hölscher1, Gregor Kemper1, Sangeth Jenthra1
1Institut für Technische und Makromolekulare Chemie, RWTH Aachen University, Worringer Weg 2, 52074, Aachen, Germany.
Abstract:
The potential of Pd/Pt complexes for catalytic carboxylation of arenes with CO2 is investigated by means of computational chemistry. Recently we reported that the bis[(2-methoxyphenyl)phosphino]-benzenesulfonamido palladium complex 1 inserts CO2 reversibly in its Pd-C(aryl) bond generating carboxylato complex 2. In the present work we study how geometric and electronic factors of various ligands and substrates influence the overall activation barrier (energy span, ES) of a potential catalytic cycle for arene carboxylation comprising this elementary step. The tendency of the key intermediates to dimerize and thus deactivating the potential catalysts is examined as well as the role of the base, which inevitably is needed to stabilize the reaction product. We show that Pd and Pt complexes I(Pd)-L16-S1 and I(Pt)-L16-S1 do not dimerize, enable the computation of complete catalytic cycles, and show interestingly low ES values of 26.8 and 24.5 kcal/mol, respectively.
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