Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 36 checked references that resolve
resolves10.3354/ame031279Dissolved organic nitrogen: a dynamic participant in aquatic ecosystems
resolves10.1038/381404a0Photochemical release of biologically available nitrogen from aquatic dissolved organic matter
resolves10.1063/1.2348868Competition between ultrafast relaxation and photoionization in excited prefluorescent states of tryptophan and indole
resolves10.1016/S1010-6030(00)00235-5Nanosecond UV laser photoionization of aqueous tryptophan: temperature dependence of quantum yield, mechanism, and kinetics of hydrated electron decay
resolves10.1063/1.555805Critical Review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals (⋅OH/⋅O− in Aqueous Solution
resolves10.1021/ja00843a004Excited state chemistry of aromatic amino acids and related peptides. III. Tryptophan
resolves10.1016/S0304-4165(02)00215-5Electron transfer oxidation of tryptophan and tyrosine by triplet states and oxidized radicals of flavin sensitizers: a laser flash photolysis study
resolves10.1021/es300142yInvestigating the Mechanism of Phenol Photooxidation by Humic Substances
resolves10.1021/es800185dIndirect Photodegradation of Dissolved Free Amino Acids: The Contribution of Singlet Oxygen and the Differential Reactivity of DOM from Various Sources
resolves10.1039/b719982aInhibitory effect of dissolved organic matter on triplet-induced oxidation of aquatic contaminants
resolves10.1021/es102212tEffect of Dissolved Organic Matter on the Transformation of Contaminants Induced by Excited Triplet States and the Hydroxyl Radical
resolves10.1021/es300485uPhenolic Antioxidants Inhibit the Triplet-Induced Transformation of Anilines and Sulfonamide Antibiotics in Aqueous Solution
resolves10.1021/es0110731Electrochemical Properties of Natural Organic Matter (NOM), Fractions of NOM, and Model Biogeochemical Electron Shuttles
resolves10.1021/es302468qLow Molecular Weight Components in an Aquatic Humic Substance As Characterized by Membrane Dialysis and Orbitrap Mass Spectrometry
resolves10.1021/es0340782Photochemical Fate of Pharmaceuticals in the Environment: Cimetidine and Ranitidine
resolves10.1021/es801847gQuantifying Interactions between Singlet Oxygen and Aquatic Fulvic Acids
resolves10.1016/S0043-1354(98)00447-3Relationships between the structure of natural organic matter and its reactivity towards molecular ozone and hydroxyl radicals
resolves10.1021/es2000694Assessing the Contribution of Free Hydroxyl Radical in Organic Matter-Sensitized Photohydroxylation Reactions
resolves10.1021/es062529nElectron Pulse Radiolysis Determination of Hydroxyl Radical Rate Constants with Suwannee River Fulvic Acid and Other Dissolved Organic Matter Isolates
resolves10.1021/es800349bQuantitative Correlation of Absolute Hydroxyl Radical Rate Constants with Non-Isolated Effluent Organic Matter Bulk Properties in Water
resolves10.1021/es0611238Aqueous Oxidation of Phenylurea Herbicides by Triplet Aromatic Ketones
resolves10.1021/es00131a008Photosensitized transformations involving electronic energy transfer in natural waters: role of humic substances
resolves10.1021/jf980737wBenzoic and Cinnamic Acid Derivatives as Antioxidants: Structure−Activity Relation
resolves10.1016/S0304-4165(02)00285-4Higher radical scavenging activities of polyphenolic antioxidants can be ascribed to chemical reactions following their oxidation
resolves10.1006/abio.2002.5577Mechanistic Study of the Oxidation of Caffeic Acid by Digital Simulation of Cyclic Voltammograms
resolves10.1021/j100155a035Kinetics and energetics of one-electron-transfer reactions involving tryptophan neutral and cation radicals
resolves10.1021/jp9930550Oxidation of Phenols by Triplet Aromatic Ketones in Aqueous Solution
resolves10.1021/es404236cReactivity Differences of Combined and Free Amino Acids: Quantifying the Relationship between Three-Dimensional Protein Structure and Singlet Oxygen Reaction Rates
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