Szakács Zoltán, Tasior Mariusz, Gryko Daniel T, Vauthey Eric
Department of Physical Chemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211, Genève 4, Switzerland.
Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224, Warsaw, Poland.
Chemphyschem. 2020 Aug 4;21(15):1718-1730. doi: 10.1002/cphc.202000253. Epub 2020 Jul 3.
Upon photoexcitation, a majority of quadrupolar dyes, developed for large two-photon absorption, undergo excited-state symmetry breaking (ES-SB) and behave as dipolar molecules. We investigate how the change of quadrupole moment upon S ←S excitation, ΔQ, influences the propensity of a dye to undergo ES-SB using a series of molecules with a A-π-D-π-A motif where D is the exceptionally electron-rich pyrrolo[3,2-b]pyrrole and A are accepting groups. Tuning of ΔQ is achieved by appending a secondary acceptor group, A', on both sides of the D core and ES-SB is monitored using a combination of time-resolved IR and broadband fluorescence spectroscopy. The results reveal a clear correlation between ΔQ and the tendency to undergo ES-SB. When A is a stronger acceptor than A', ES-SB occurs already in non-dipolar but quadrupolar solvents. When A and A' are identical, ES-SB is only partial even in highly dipolar solvents. When A is a weaker acceptor than A', the orientation of ΔQ changes, ES-SB is observed in dipolar solvents only and involves major redistribution of the excitation over the D-π-A and D-A' branches of the dye.
在光激发下,为实现大的双光子吸收而开发的大多数四极染料会经历激发态对称性破缺(ES-SB),并表现为偶极分子。我们使用一系列具有A-π-D-π-A结构的分子来研究S←S激发时四极矩的变化ΔQ如何影响染料发生ES-SB的倾向,其中D是特别富电子的吡咯并[3,2-b]吡咯,A是受体基团。通过在D核的两侧连接一个二级受体基团A'来调节ΔQ,并使用时间分辨红外光谱和宽带荧光光谱相结合的方法监测ES-SB。结果揭示了ΔQ与发生ES-SB的倾向之间存在明显的相关性。当A是比A'更强的受体时,ES-SB已经在非偶极但四极的溶剂中发生。当A和A'相同时,即使在高度偶极的溶剂中,ES-SB也只是部分发生。当A是比A'更弱的受体时,ΔQ的方向会改变,ES-SB仅在偶极溶剂中观察到,并且涉及激发在染料的D-π-A和D-A'分支上的主要重新分布。