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Solvation shift of a conical intersection in clusters of excited tetrakis(dimethyl amino)ethylene with ammonia and acetonitrile molecules

机译:在激发的四(二甲基氨基)乙烯簇与氨和乙腈分子的锥形交叉点的溶剂化转移

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摘要

A supersonic expansion of the title molecule (TDMAE) with helium and polar solvent molecules S (ammonia or acetonitrile) generates TDAME(S)10 clusters. By applying the femtosecond pump–probe technique, a wavepacket is launched on the S1 potential energy surface of TDMAE. The electronic configuration of TDMAE changes from valence V(ππ*) to Zwitterionic C+C− when the wavepacket passes in the vicinity of a conical intersection. While argon as solvent slows down this switch by an inertial effect, the present polar molecules move the conical intersection, reduce the length of the way to access it and accelerate the corresponding V-to-Z energy transfer.
机译:用氦和极性溶剂分子S(氨或乙腈)对标题分子(TDMAE)进行超音速膨胀,生成TDAME(S)10簇。通过应用飞秒泵浦探针技术,在TDMAE的S1势能面上发射了一个波包。当波包在圆锥形交叉点附近通过时,TDMAE的电子构型从化合价V(ππ*)变为两性离子C + C-。尽管作为溶剂的氩气通过惯性效应减慢了这种转换的速度,但当前的极性分子移动了圆锥形的相交点,缩短了进入它的方式的长度,并加快了相应的V到Z的能量转移。

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