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Origin of Panchromaticity in Multichromophore–Tetrapyrrole Arrays

2018; American Chemical Society; Volume: 122; Issue: 36 Linguagem: Inglês

10.1021/acs.jpca.8b06815

1520-5215

Jonathan M. Yuen, James R. Diers, Eric J. Alexy, Arpita Roy, Amit Kumar Mandal, Hyun Suk Kang, Dariusz M. Niedzwiedzki, Christine Kirmaier, Jonathan S. Lindsey, David F. Bocian, Dewey Holten,

Photochemistry and Electron Transfer Studies

Panchromatic absorbers that have robust photophysical properties enable new designs for molecular-based light-harvesting systems. Herein, we report experimental and theoretical studies of the spectral, redox, and excited-state properties of a series of perylene-monoimide-ethyne-porphyrin arrays wherein the number of perylene-monoimide units is stepped from one to four. In the arrays, a profound shift of absorption intensity from the strong violet-blue (B y and B x) bands of typical porphyrins into the green, red, and near-infrared (Q x and Q y) regions stems from mixing of chromophore and tetrapyrrole molecular orbitals (MOs), which gives multiplets of MOs having electron density spread over the entire array. This reduces the extensive mixing between porphyrin excited-state configurations and the transition-dipole addition and subtraction that normally leads to intense B and weak Q bands. Reduced configurational mixing derives from moderate effects of the ethyne and perylene on the MO energies and a more substantial effect of electron-density delocalization to reduce the configuration-interaction energy. Quantitative oscillator-strength analysis shows that porphyrin intensity is also shifted into the perylene-like green-region absorption and that the ethyne linkers lend absorption intensity. The reduced porphyrin configurational mixing also endows the S1 state with bacteriochlorin-like properties, including a 1-5 ns lifetime.