Photocatalytic Carbon Disulfide Production via Charge Transfer Quenching of Quantum Dots

Christopher M. Bernt, Peter T. Burks, Anthony W. DeMartino, Agustin E. Pierri, Elizabeth S. Levy, David F. Zigler, Peter C. Ford

Journal of the American Chemical Society · 2013 · 51 citations · 17 references

DOIFull text

Open access

Concepts

Abstract

Carbon disulfide, a potentially therapeutic small molecule, is generated via oxidative cleavage of 1,1-dithiooxalate (DTO) photosensitized by CdSe quantum dots (QDs). Irradiation of DTO-QD conjugates leads to λ(irr) independent photooxidation with a quantum yield of ~4% in aerated pH 9 buffer solution that drops sharply in deaerated solution. Excess DTO is similarly decomposed, indicating labile exchange at the QD surfaces and a photocatalytic cycle. Analogous photoreaction occurs with the O-tert-butyl ester (t)BuDTO in nonaqueous media. We propose that oxidation is initiated by hole transfer from photoexcited QD to surface DTO and that these substrates are a promising class of photocleavable ligands for modifying QD surface coordination.

References

17