Computational Study Illustrating NCN-Palladium(IV) Involvement in Generating Pd0 Species to Facilitate Pd0/PdII Heck-Type Catalysis with Diphenyliodine(III) Species

Date

Authors

Canty, Allan J.
Ariafard, Alireza

Journal Title

Journal ISSN

Volume Title

Publisher

Access Statement

Research Projects

Organizational Units

Journal Issue

Abstract

Density functional theory has been applied in a mechanistic study of the role of pincer complex PdII(NCN-N,C,N)(O2CPh-O) ([NCN]- = [2,6-(Me2NCH2)2C6H3]−) (3) in Heck-type catalysis in the presence of diphenyliodine(III) triflate as the oxidative arylating agent for CH2═CHAr and bicarbonate as the base to afford PhCH═CHAr (Ar = p-BrC6H4). The initially formed palladium(IV) complex PhPd(NCN-N,C,N)(OBz···HOCO2-O,O) (9) (ΔG‡ 31.6 kcal/mol) undergoes Ph···Cipso reductive elimination to form PdII{NC(Ph)N-N,C,N}(OBz···HOCO2-O,O) (11) (ΔG‡ 25.6 kcal/mol), which is reduced by bicarbonate to form palladium(0) species. Reduction to Pd0 occurs via deprotonation of one NMe2 group by bicarbonate to provide a “-CH2-N(Me)-CH2-PdII″ moiety (ΔG‡ 23.6 kcal/mol) followed by nucleophilic attack on this moiety by bicarbonate to give a Pd0 product with a “-CH2-NMe(CH2OCO2H)″ group (ΔG‡ 14.5 kcal/mol). The Pd0 complex undergoes exceptionally facile oxidative addition by Ph2I(HCO3) (ΔG‡ = 5.1 kcal/mol). Modeling the Pd0 complex as [Pd(benzene)(O2CPh)]− provides a similar result (ΔG‡ = 5.6 kcal/mol), allowing entry to PhPdII species to be able to undergo migratory insertion for CH2═CAr (ΔG‡ = 14.4 kcal/mol) and β-hydride elimination (ΔG‡ = 16.2 kcal/mol) processes of Pd0/PdII Heck-type catalysis. Activation barriers for reduction of PdIV to Pd0, and in the Heck-type process, are lower than the initial oxidation to form PdIV species, ensuring that only a small quantity of PdII(NCN)(OBz) (3) is consumed, in accord with its presence on completion of catalysis. Computational studies of PdIV-mediated Heck-type catalysis revealed energetically unfavorable processes and a preference for the formation of CH2═C(Ar)Ph rather than the experimentally reported PhCH═CHAr. This study reveals the role of a pincer complex as a precatalyst, the oxidation of PdII to PdIV followed by reductive elimination, the role of bicarbonate in reducing PdII to Pd0, the extremely facile oxidative addition of a diaryliodine(III) reagent to Pd0, and the selectivity differences in migratory insertion for PdII and PdIV centers.

Description

Keywords

Citation

Source

Organometallics

Book Title

Entity type

Publication

Access Statement

License Rights

Restricted until