Loading…
Homomolecular Triplet-Triplet Annihilation in Metalloporphyrin Photosensitizers
Metalloporphyrins are ubiquitous in their applications as triplet photosensitizers, particularly for promoting sensitized photochemical upconversion processes. In this study, bimolecular excited state triplet-triplet quenching kinetics, termed homomolecular triplet-triplet annihilation (HTTA), exhib...
Saved in:
Published in: | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2024-09, Vol.128 (36), p.7648-7656 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Metalloporphyrins are ubiquitous in their applications as triplet photosensitizers, particularly for promoting sensitized photochemical upconversion processes. In this study, bimolecular excited state triplet-triplet quenching kinetics, termed homomolecular triplet-triplet annihilation (HTTA), exhibited by the traditional triplet photosensitizers-zinc(II) tetraphenylporphyrin (ZnTPP), palladium(II) octaethylporphyrin (PdOEP), platinum(II) octaethylporphyrin (PtOEP), and platinum(II) tetraphenyltetrabenzoporphyrin (PtTPBP)─were revealed using conventional transient absorption spectroscopy. Nickel(II) tetraphenylporphyrin was used as a control sample as it is known to be rapidly quenched intramolecularly through ligand-field state deactivation and, therefore, cannot result in triplet-triplet annihilation (TTA). The single wavelength transients associated with the metalloporphyrin triplet excited state decay─measured as a function of incident laser pulse energy in toluene─were well modeled using parallel first- and second-order kinetics, consistent with HTTA being operable. The combined transient kinetic data enabled the determination of the first-order rate constants (
) for excited triplet decay in ZnTPP (4.0 × 10
s
), PdOEP (3.6 × 10
s
), PtOEP (1.2 × 10
s
), and PtTPBP (2.1 × 10
s
) as well as the second-order rate constant (
) for HTTA in ZnTPP (5.5 × 10
M
s
), PdOEP (1.1 × 10
M
s
), PtOEP (7.1 × 10
M
s
), and PtTPBP (1.6 × 10
M
s
). In most instances, triplet excited state extinction coefficients are either reported for the first time or have been revised using ultrafast transient absorption spectroscopy and singlet depletion: ZnTPP (78,000 M
cm
) at 470 nm, PdOEP (67,000 M
cm
) at 430 nm, PtOEP (51,000 M
cm
) at 418 nm, and PtTPBP (100,000 M
cm
) at 460 nm. The combined experimental results establish competitive time scales for homo- and heteromolecular TTA rate constants, implying the significance of considering HTTA processes in future research endeavors harnessing TTA photochemistry using common metalloporphyrin photosensitizers. |
---|---|
ISSN: | 1089-5639 1520-5215 1520-5215 |
DOI: | 10.1021/acs.jpca.4c05052 |