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Excited states of porphyrin and porphycene aggregates: Computational insights

[Display omitted] •Density functional and time-dependent density functional theory applied to porphyrin and porphycene aggregates.•Effect of different aggregation modes on electronic spectra investigated.•Long-range corrected functionals essential to describe aggregates in ground and excited states....

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Published in:Computational and theoretical chemistry 2014-07, Vol.1040-1041, p.274-286
Main Authors: Bergendahl, L. Therese, Paterson, Martin J.
Format: Article
Language:English
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Summary:[Display omitted] •Density functional and time-dependent density functional theory applied to porphyrin and porphycene aggregates.•Effect of different aggregation modes on electronic spectra investigated.•Long-range corrected functionals essential to describe aggregates in ground and excited states.•TD-DFT better reproduces expected exitonic coupling pattern for aggregates as opposed to J-aggregates.•Natural transition orbitals excellent tool at characterising complex excited states in aggregate systems. Computational studies of the structure and electronic spectroscopy of porphyrin and porphycene aggregates has been carried out using Density Functional Theory. A comparison of different DFT approaches has been undertaken, and we show that the proper treatment must include dispersion, here through the B97-D functional, to correctly find bound species. Accurate prediction of absorption spectra for aggregates is possible if care is taken when choosing an appropriate methodology. Excitonic bands are observed in the aggregates, which highlight the importance of using long-range corrected DFT functionals in order to capture aggregate excitations. Excited state stabilisation models developed in the past, and used for spectra analysis in the case of aggregation, are shown to be qualitatively valid for excitations along an aggregation slipping coordinate. It is shown that natural transition orbitals provide the best framework for analysing aggregate spectra.
ISSN:2210-271X
DOI:10.1016/j.comptc.2014.03.014