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Amy L. McCarty

Researcher at Wichita State University

Publications -  18
Citations -  918

Amy L. McCarty is an academic researcher from Wichita State University. The author has contributed to research in topics: Porphyrin & Electron transfer. The author has an hindex of 14, co-authored 18 publications receiving 889 citations.

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Energy Transfer Followed by Electron Transfer in a Supramolecular Triad Composed of Boron Dipyrrin, Zinc Porphyrin, and Fullerene: A Model for the Photosynthetic Antenna-Reaction Center Complex

TL;DR: The first example of a working model of the photosynthetic antenna-reaction center complex, constructed via self-assembled supramolecular methodology, is reported, and it is reported that the important feature of the present model system is its relative "simplicity".
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Supramolecular Triads Formed by Axial Coordination of Fullerene to Covalently Linked Zinc Porphyrin−Ferrocene(s): Design, Syntheses, Electrochemistry, and Photochemistry

TL;DR: In this article, photo-induced charge-separation and charge-recombination processes were examined in the dyads and triads by means of time-resolved transient absorption and fluorescence lifetime measurements.
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Effect of axial ligation or π-π-type interactions on photochemical charge stabilization in two-point bound supramolecular porphyrin-fullerene conjugates

TL;DR: Two types of structurally well-defined, self-assembled zinc porphyrin-fullerene conjugates were formed by "two-point" binding strategies to probe the effect of axial ligation or pi-pi-type interactions on the photochemical charge stabilization in the supramolecular dyads.
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Self-assembled via axial coordination magnesium porphyrin-imidazole appended fullerene dyad: spectroscopic, electrochemical, computational, and photochemical studies.

TL;DR: Spectroscopic, redox, and electron transfer reactions of a self-assembled donor-acceptor dyad formed by axial coordination of magnesium meso-tetraphenylporphyrin and fulleropyrrolidine appended with an imidazole coordinating ligand were investigated and suggested an excellent opportunity to utilize the charge-separated state for further electron-mediating processes.
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Highly nonplanar, electron deficient, N-substituted tetra-oxocyclohexadienylidene porphyrinogens: structural, computational, and electrochemical investigations.

TL;DR: Electrochemical analyses indicate that the N-benzylated meso-tetra (oxo-cyclohexadienylidene) porphyrinogens can be considered as quinones conjugated via the unsaturated tetrapyrrolic macrocycle and ab initio molecular orbital calculations at the B3LYP/3-21G() level confirmed the high degree of conjugation.