Stabilization of Super Electrophilic Pd+2 Cations in Small-Pore SSZ-13 Zeolite

We provide the first observation and characterization of super-electrophilic metal cations on a solid support. For Pd/SSZ-13 the results of our combined experimental (FTIR, XPS, HAADF-STEM) and density functional theory study reveal that Pd ions in zeolites, previously identified as Pd +3 and Pd +4 , are in fact present as super electrophilic Pd +2 species (charge-transfer complex/ion pair with the negatively charged framework oxygens). In this contribution we re-assign the spectroscopic signatures of these species, discuss the unusual coordination environment of “naked” (ligand-free) super-electrophilic Pd +2 in SSZ-13, and their complexes with CO and NO. With CO, non-classical, highly positive [Pd(CO) 2 ] 2+ ions are formed with the zeolite framework acting as a weakly coordinating anion (ion pairs). Non-classical carbonyl complexes also form with Pt +2 and Ag + in SSZ-13. The Pd +2 (CO) 2 complex is remarkably stable in zeolite cages even in the presence of water. Dicarbonyl and nitrosyl Pd +2 complexes, in turn, serve as precursors to the synthesis of previously inaccessible Pd +2 -carbonyl-olefin [Pd(CO)(C 2 H 4 )] and -nitrosyl-olefin [Pd(NO)(C 2 H 4 )] complexes. Overall, we show that zeolite framework can stabilize super electrophilic metal (Pd) cations, and show the new chemistry of Pd/SSZ-13 system with implications for adsorption and catalysis.