Full kinetics investigation of the formation reaction of phosphonate esters in the gas-phase: a theoretical study

In the present work, the proposed multiple-mechanisms have been investigated theoretically for the reaction between triphenyl phosphite and dimethyl acetylenedicarboxylate in the presence of N-H acid such as aniline for generation of phosphonate esters using ab initio molecular orbital theory in gas phase. The profile of the potential energy surface was constructed at the HF/6-311G(d,p) level of theory. The kinetics of the gas phase reaction was studied by evaluating the reaction path of various mechanisms. Between 12 speculative proposed mechanisms {step1, step2 (with four possibilities), step3 (with three possibilities), and step4} only the third speculative mechanism was recognized as a desirable mechanism. Theoretical kinetics data involving k and E a , activation (ΔG ‡, ΔS ‡ and ΔH ‡), and thermodynamic parameters (ΔG°, ΔS° and ΔH °) were calculated for each step of the various mechanisms. Step1 of the desirable mechanism was identified as the rate determining step. Comparison of the theoretical desirable mechanism with the rate law that has been previously obtained by UV spectrophotometry experiments indicated that the results are in good agreement.