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Two-Dimensional Electronic Spectroscopy Reveals Dynamics and Mechanisms of Solvent-Driven Inertial Relaxation in Polar BODIPY Dyes
Author(s) -
Luca Bolzonello,
Annalisa Polo,
Andrea Volpato,
Elena Meneghin,
Massimiliano Cordaro,
Mariachiara Trapani,
Mariagrazia Fortino,
Alfonso Pedone,
Maria Angela Castriciano,
Elisabetta Collini
Publication year - 2018
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.7b03393
Subject(s) - chemical physics , bodipy , femtosecond , chemistry , relaxation (psychology) , intramolecular force , stokes shift , spectroscopy , molecule , molecular physics , physics , optics , fluorescence , quantum mechanics , psychology , social psychology , laser , organic chemistry , stereochemistry
In this work, we demonstrate the use of two-dimensional electronic spectroscopy (2DES) to study the mechanism and time scale of the femtosecond Stokes shift dynamics in molecules characterized by intramolecular charge transfer, such as distyryl-functionalized boron dipyrromethene (BODIPY) molecules. The obtained results demonstrate that 2DES allows clear and direct visualization of the phenomenon. The analysis of the 2D data in terms of 2D frequency-frequency decay associated maps provides indeed not only the time scale of the relaxation process but also the starting and the final point of the energy flow and the associated reorganization energy, identified by looking at the coordinates of a negative signature below the diagonal. The sensitivity of the 2DES technique to vibrational coherence dynamics also allowed the identification of a possible relaxation mechanism involving specific interaction between a vibrational mode of the dye and the solvent.

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