Reversible Uptake of CO2 by Pincer Ligand Supported Dimetallynes.

Abstract

We report on the reversible uptake of carbon dioxide by dimetallynes featuring ancillary hemi-labile pincer ligands. Insertion into the Ge-Ge/Sn-Sn bonds yields species containing an E(CO2 )E unit, with the mode of ligation of the CO2 fragment determined crystallographically being found to be dependent on the identity of the Group 14 element. The thermodynamics of CO2 uptake/loss can be established through VT NMR (ΔH°=+24.6(2.3) kJ mol-1 , ΔS°=+64.9(3.8) J mol-1 K-1 , ΔG°298 =+5.3(1.9) kJ mol-1 for the loss of CO2 in the Ge case), and the chemical consequences of reversibility demonstrated by thermodynamically-controlled exchange reactions.