Barlow Kyle, Eng Julien, Ivalo Iona, Coletta Marco, Brechin Euan K, Penfold Thomas J, Johansson J Olof
EaStCHEM School of Chemistry, University of Edinburgh, David Brewster Road, EH9 3FJ, Edinburgh, UK.
Chemistry, School of Natural and Environmental Sciences, Newcastle University, Newcastle Upon Tyne, UK.
Dalton Trans. 2022 Jul 19;51(28):10751-10757. doi: 10.1039/d2dt00889k.
Ultrafast transient absorption spectra were recorded for [Mn(terpy)X], where X = Cl, F, and N, to explore photoinduced switching from axial to equatorial Jahn-Teller (JT) distortion. Strong oscillations were observed in the transients, corresponding to a wavepacket on the excited-state potential energy surface with oscillation frequency around 115 cm for all three complexes. Multireference quantum chemistry calculations indicate that the reaction coordinate is a pincer-like motion of the terpyridine ligand arising from bond length changes in the excited state due to the JT switch. We observed long dephasing times of the wavepacket, with times of 620 fs for [Mn(terpy)Cl], 450 fs for [Mn(terpy)F], and 370 fs for [Mn(terpy)(N)]. The dephasing time of these coherences decreases with an increasing number of vibrational modes at lower energy than the mode dominating the reaction coordinate, suggesting they act as an effective bath to dissipate the excess energy obtained from photoexcitation.
记录了[Mn(terpy)X](其中X = Cl、F和N)的超快瞬态吸收光谱,以探索从轴向到赤道面的 Jahn-Teller(JT)畸变的光致开关。在瞬态中观察到强烈振荡,对应于所有三种配合物在激发态势能面上的一个波包,其振荡频率约为115 cm⁻¹。多参考量子化学计算表明,反应坐标是由于JT开关导致激发态键长变化而产生的三联吡啶配体的钳状运动。我们观察到波包的长退相时间,[Mn(terpy)Cl]为620 fs,[Mn(terpy)F]为450 fs,[Mn(terpy)(N)]为370 fs。这些相干性的退相时间随着比主导反应坐标的模式能量更低的振动模式数量增加而减小,这表明它们起到了有效浴的作用,以耗散光激发获得的多余能量。