Spin-Vibronic Control of Intersystem Crossing in Iodine-Substituted Heptamethine Cyanines

Investor logo
Investor logo
Investor logo

Warning

This publication doesn't include Faculty of Economics and Administration. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

TOVTIK Radek MUCHOVA Eva ŠTACKOVÁ Lenka SLAVÍČEK Petr KLÁN Petr

Year of publication 2023
Type Article in Periodical
Magazine / Source Journal of Organic Chemistry
MU Faculty or unit

Faculty of Science

Citation
web https://pubs.acs.org/doi/10.1021/acs.joc.3c00005
Doi http://dx.doi.org/10.1021/acs.joc.3c00005
Keywords NEAR-INFRARED FLUORESCENCE; DENSITY-FUNCTIONAL THEORY; SINGLET OXYGEN; QUANTUM YIELD; TRIPLET-STATE; DYES; PHOTOPHYSICS; PHOTOCHEMISTRY; TRANSFORMATION; SPECTROSCOPY
Attached files
Description Spin-orbit coupling between electronic states of different multiplicity can be strongly coupled to molecular vibrations, and this interaction is becoming recognized as an important mechanism for controlling the course of photochemical reactions. Here, we show that the involvement of spin-vibronic coupling is essential for understanding the photophysics and photochemistry of heptamethine cyanines (Cy7), bearing iodine as a heavy atom in the C3 ' position of the chain and/or a 3H-indolium core, as potential triplet sensitizers and singlet oxygen producers in methanol and aqueous solutions. The sensitization efficiency was found to be an order of magnitude higher for the chain substituted than the 3H-indolium core-substituted derivatives. Our ab initio calculations demonstrate that while all optimal structures of Cy7 are characterized by negligible spin-orbit coupling (tenths of cm(-1)) with no dependence on the position of the substituent, molecular vibrations lead to its significant increase (tens of cm(-1) for the chain-substituted cyanines), which allowed us to interpret the observed position dependence.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.