K
Kristopher McNeill
Researcher at ETH Zurich
Publications - 193
Citations - 12134
Kristopher McNeill is an academic researcher from ETH Zurich. The author has contributed to research in topics: Singlet oxygen & Hydroxyl radical. The author has an hindex of 53, co-authored 184 publications receiving 9821 citations. Previous affiliations of Kristopher McNeill include University of St. Thomas (Minnesota) & University of California.
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Photochemical fate of sulfa drugs in the aquatic environment: sulfa drugs containing five-membered heterocyclic groups.
TL;DR: This study indicates that similarly structured antibiotics will be subject to a wide range of photodegradation rates with sulfathiazole degrading relatively quickly, sulfisoxazole and sulfamethizole degrading moderately, and sulfanilic acid degrading much more slowly.
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Photochemical fate of pharmaceuticals in the environment: Naproxen, diclofenac, clofibric acid, and ibuprofen
TL;DR: In this article, the aqueous photochemistry of four pharmaceutical compounds detected in surface waters (naproxen, diclofenac, ibuprofen, and clofibric acid) was investigated in purified (Milli-Q) water and in Mississippi River water (MRW).
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Photodegradation of pharmaceuticals in the aquatic environment: A review
TL;DR: A review with 310 references summarizes the current knowledge of the photochemical behavior of pharmaceuticals and highlights the use of the fundamental photochemistry and phototoxicity literature to help understand and predict the aquatic fate of pharmaceutical drugs.
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Triplet state dissolved organic matter in aquatic photochemistry: reaction mechanisms, substrate scope, and photophysical properties
TL;DR: It is proposed that through the use of appropriate sets of probe compounds and model photosensitizers an improved estimation of the distribution of triplet energies and one-electron reduction potentials of 3CDOM* can be achieved.
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Triplet-sensitized photodegradation of sulfa drugs containing six-membered heterocyclic groups: identification of an SO2 extrusion photoproduct.
TL;DR: Photodegradation of the sulfa drugs in a natural water sample was significantly enhanced relative to the degradation in deionized water, with the exception of sulfadimethoxine, which indicated an indirect photochemical process that was identified through the use of quenchers to be attributable to interaction with triplet excited-state dissolved organic matter (3DOM).