Bioinspired, Multidisciplinary, Iterative Catalyst Design Creates the Highest Performance Peroxidase Mimics and the Field of Sustainable Ultradilute Oxidation Catalysis (SUDOC)
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Longzhu Q. Shen | A. Ryabov | Julia A. Taylor | F. V. vom Saal | Genoa R. Warner | T. J. Collins | M. Hendrich | T. Pintauer | M. Mills | Yogesh Somasundar | Kyle C. Jansen | Evan Z. Kaaret | Cindy Weng | Abigail E. Burton | Gabrielle Pros | S. Biswas
[1] Howard Hu,et al. Prenatal fluoride exposure and attention deficit hyperactivity disorder (ADHD) symptoms in children at 6-12 years of age in Mexico City. , 2018, Environment international.
[2] Longzhu Q. Shen,et al. Structural, Mechanistic, and Ultradilute Catalysis Portrayal of Substrate Inhibition in the TAML-Hydrogen Peroxide Catalytic Oxidation of the Persistent Drug and Micropollutant, Propranolol. , 2018, Journal of the American Chemical Society.
[3] B. Glass,et al. Advanced oxidation process-mediated removal of pharmaceuticals from water: A review. , 2018, Journal of environmental management.
[4] M. Ehrampoush,et al. Impact of Drinking Water Fluoride on Human Thyroid Hormones: A Case- Control Study , 2018, Scientific Reports.
[5] Longzhu Q. Shen,et al. Iron(III) Ejection from a "Beheaded" TAML Activator: Catalytically Relevant Mechanistic Insight into the Deceleration of Electrophilic Processes by Electron Donors. , 2017, Inorganic chemistry.
[6] A. Ryabov,et al. Targeting of High-Valent Iron-TAML Activators at Hydrocarbons and Beyond. , 2017, Chemical reviews.
[7] R. Gil,et al. Homogeneous Catalysis Under Ultradilute Conditions: TAML/NaClO Oxidation of Persistent Metaldehyde. , 2017, Journal of the American Chemical Society.
[8] A. Ryabov,et al. A "Beheaded" TAML Activator: A Compromised Catalyst that Emphasizes the Linearity between Catalytic Activity and pKa. , 2016, Inorganic chemistry.
[9] Ana M Soto,et al. Minireview: Endocrine Disruptors: Past Lessons and Future Directions. , 2016, Molecular endocrinology.
[10] A. Ryabov,et al. Unifying Evaluation of the Technical Performances of Iron-Tetra-amido Macrocyclic Ligand Oxidation Catalysts. , 2016, Journal of the American Chemical Society.
[11] A C Gore,et al. EDC-2: The Endocrine Society's Second Scientific Statement on Endocrine-Disrupting Chemicals. , 2015, Endocrine reviews.
[12] Judy Strickland,et al. A Curated Database of Rodent Uterotrophic Bioactivity , 2015, Environmental health perspectives.
[13] Longzhu Q. Shen,et al. Removal of ecotoxicity of 17α-ethinylestradiol using TAML/peroxide water treatment , 2015, Scientific Reports.
[14] A. Ryabov,et al. Reactivity and operational stability of N-tailed TAMLs through kinetic studies of the catalyzed oxidation of orange II by H2 O2 : synthesis and X-ray structure of an N-phenyl TAML. , 2015, Chemistry.
[15] C. Stamm,et al. Reducing the discharge of micropollutants in the aquatic environment: the benefits of upgrading wastewater treatment plants. , 2014, Environmental science & technology.
[16] A. Ryabov,et al. Estimation of rate constants in nonlinear reactions involving chemical inactivation of oxidation catalysts , 2014, Journal of Mathematical Chemistry.
[17] Robert L. Tanguay,et al. Zebrafish Assays as Developmental Toxicity Indicators in The Design of TAML Oxidation Catalysts. , 2013, Green chemistry : an international journal and green chemistry resource : GC.
[18] L. Giudice,et al. State of the Science of Endocrine Disrupting Chemicals - 2012 , 2012 .
[19] John P Sumpter,et al. Predicted‐no‐effect concentrations for the steroid estrogens estrone, 17β‐estradiol, estriol, and 17α‐ethinylestradiol , 2012, Environmental toxicology and chemistry.
[20] Laura N. Vandenberg,et al. Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses. , 2012, Endocrine reviews.
[21] A. Ryabov,et al. Designing green oxidation catalysts for purifying environmental waters. , 2010, Journal of the American Chemical Society.
[22] Brian C. Berry,et al. Cycloaddition of CO2 to Epoxides Using a Highly Active Co(III) Complex of Tetraamidomacrocyclic Ligand , 2010 .
[23] A. Ryabov,et al. Design of more powerful iron-TAML peroxidase enzyme mimics. , 2009, Journal of the American Chemical Society.
[24] Evan S. Beach,et al. Activation of Hydrogen Peroxide by an Fe-TAML Complex in Strongly Alkaline Aqueous Solution: Homogeneous Oxidation Catalysis with Industrial Significance , 2009 .
[25] C. Cramer,et al. Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions. , 2009, The journal of physical chemistry. B.
[26] Benjamin D. Stanford,et al. Pharmaceuticals and endocrine disrupting compounds in U.S. drinking water. , 2009, Environmental science & technology.
[27] A. Ryabov,et al. Catalase-peroxidase activity of iron(III)-TAML activators of hydrogen peroxide. , 2008, Journal of the American Chemical Society.
[28] A. Ryabov,et al. Mechanistically inspired design of Fe(III)-TAML peroxide-activating catalysts. , 2008, Journal of the American Chemical Society.
[29] Sushil K. Khetan,et al. Human pharmaceuticals in the aquatic environment: a challenge to Green Chemistry. , 2007, Chemical reviews.
[30] Karen A Kidd,et al. Collapse of a fish population after exposure to a synthetic estrogen , 2007, Proceedings of the National Academy of Sciences.
[31] A. Ryabov,et al. Activity-stability parameterization of homogeneous green oxidation catalysts. , 2006, Chemistry.
[32] R. Schwarzenbach,et al. The Challenge of Micropollutants in Aquatic Systems , 2006, Science.
[33] P. Berget,et al. "Green" oxidation catalysis for rapid deactivation of bacterial spores. , 2006, Angewandte Chemie.
[34] W. Tsang,et al. Acyl vs sulfonyl transfer in N-acyl beta-sultams and 3-oxo-beta-sultams. , 2004, Organic letters.
[35] Duane E. Prasuhn,et al. Understanding the mechanism of H(+)-induced demetalation as a design strategy for robust iron(III) peroxide-activating catalysts. , 2003, Journal of the American Chemical Society.
[36] T. J. Collins. TAML oxidant activators: a new approach to the activation of hydrogen peroxide for environmentally significant problems. , 2002, Accounts of chemical research.
[37] Terry Collins,et al. Toward Sustainable Chemistry , 2001, Science.
[38] M. Page,et al. Reactivity and Mechanism in the Hydrolysis of β-Sultams , 2000 .
[39] T. Ternes,et al. Pharmaceuticals and personal care products in the environment: agents of subtle change? , 1999, Environmental health perspectives.
[40] C. P. Horwitz,et al. Ligand Design Approach for Securing Robust Oxidation Catalysts , 1998 .
[41] T. J. Collins. Designing Ligands for Oxidizing Complexes , 1994 .
[42] A. Becke. Density-functional thermochemistry. III. The role of exact exchange , 1993 .
[43] D. W. Margerum. Metal peptide complexes , 1983 .
[44] K. Chellappa,et al. Ligand effects on the thermodynamic stabilization of copper(III)-peptide complexes. , 1977, Journal of the American Chemical Society.
[45] W. Carmody. Easily prepared wide range buffer series , 1963 .
[46] P. George. The chemical nature of the second hydrogen peroxide compound formed by cytochrome c peroxidase and horseradish peroxidase. I. Titration with reducing agents. , 1953, The Biochemical journal.
[47] T. J. Collins,et al. Review of the twenty-three year evolution of the first university course in green chemistry: teaching future leaders how to create sustainable societies , 2017 .
[48] G. B. Buck Louis,et al. Male Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility. , 2016, Physiological reviews.
[49] R. Moreira,et al. Kinetics and mechanism of hydrolysis of N-amidomethylsulfonamides , 2001 .
[50] J. Sumpter,et al. Endocrine disruption in wildlife: a critical review of the evidence. , 1998, Critical reviews in toxicology.