Demystifying the Origin of Vibrational Coherence Transfer Between the S1 and T1 States of the Pt-pop Complex

Abstract

We demonstrate that spin-vibronic coupling is the most significant mechanism in vibrational coherence transfer (VCT) from the singlet (S₁) to the triplet (T₁) state of the [Pt₂(P₂O₅H₂)₄]^4– complex. Our time-dependent correlation function-based study shows that the rate of intersystem crossing (<i>k</i>_ISC) through direct spin–orbit coupling is negligibly small, making VCT vanishingly small due to the ultrashort decoherence time (2.5 ps). However, the inclusion of the spin-vibronic contribution to the net <i>k</i>_ISC in selective normal modes along the Pt–Pt axis increases the <i>k</i>_ISC to such an extent that VCT becomes feasible. Our results suggest that <i>k</i>_ISC for the S₁ →T₂ (τ_ISC = 1.084 ps) is much faster than the S₁ → T₁ (τ_ISC = 763.4 ps) and S₁ → T₃ (τ_ISC = 13.38 ps) in CH3CN solvent, indicating that VCT is possible from the low-lying excited singlet (S₁) to the triplet (T₁) state through the intermediate T₂ state. This is the first example where VCT occurs solely due to spin-vibronic interactions. This finding can pave the way for new types of photocatalysis.