Giovanny A Parada - Publications

Affiliations: 
The College of New Jersey, Ewing Township, NJ, United States 
Area:
PCET

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Pettersson Rimgard B, Tao Z, Parada GA, Cotter LF, Hammes-Schiffer S, Mayer JM, Hammarström L. Proton-coupled energy transfer in molecular triads. Science (New York, N.Y.). abq5173. PMID 35862490 DOI: 10.1126/science.abq5173  0.696
2021 Agarwal RG, Coste SC, Groff BD, Heuer AM, Noh H, Parada GA, Wise CF, Nichols EM, Warren JJ, Mayer JM. Free Energies of Proton-Coupled Electron Transfer Reagents and Their Applications. Chemical Reviews. PMID 34928136 DOI: 10.1021/acs.chemrev.1c00521  0.695
2021 Cattaneo M, Parada GA, Tenderholt AL, Kaminsky W, Mayer JM. Structural, Electronic and Thermochemical preference for multi-PCET reactivity of Ruthenium(II)-Amine and Ruthenium(IV)-Amido Complexes. European Journal of Inorganic Chemistry. 2021: 4042. PMID 34776777 DOI: 10.1002/ejic.202100761  0.587
2021 Cotter LF, Rimgard BP, Parada GA, Mayer JM, Hammarström L. Solvent and Temperature Effects on Photoinduced Proton-Coupled Electron Transfer in the Marcus Inverted Region. The Journal of Physical Chemistry. A. PMID 34432465 DOI: 10.1021/acs.jpca.1c05764  0.675
2020 Shen Z, Walker MM, Chen S, Parada GA, Chu DM, Dongbang S, Mayer JM, Houk KN, Ellman JA. General Light-Mediated, Highly Diastereoselective Piperidine Epimerization: From Most Accessible to Most Stable Stereoisomer. Journal of the American Chemical Society. PMID 33373212 DOI: 10.1021/jacs.0c11911  0.492
2019 Parada GA, Goldsmith ZK, Kolmar S, Pettersson Rimgard B, Mercado BQ, Hammarström L, Hammes-Schiffer S, Mayer JM. Concerted proton-electron transfer reactions in the Marcus inverted region. Science (New York, N.Y.). PMID 30975771 DOI: 10.1126/Science.Aaw4675  0.695
2018 Darcy JW, Koronkiewicz B, Parada GA, Mayer JM. A Continuum of Proton-Coupled Electron Transfer Reactivity. Accounts of Chemical Research. PMID 30234963 DOI: 10.1021/Acs.Accounts.8B00319  0.602
2018 Bowring MA, Bradshaw LR, Parada GA, Pollock TP, Fernández-Terán RJ, Kolmar SS, Mercado BQ, Schlenker CW, Gamelin DR, Mayer JM. Activationless Multiple-Site Concerted Proton-Electron Tunneling. Journal of the American Chemical Society. PMID 29847111 DOI: 10.1021/Jacs.8B04455  0.596
2017 Schlotthauer T, Parada GA, Görls H, Ott S, Jäger M, Schubert US. Asymmetric Cyclometalated Ru(II) Polypyridyl-Type Complexes with π-Extended Carbanionic Donor Sets. Inorganic Chemistry. PMID 28677955 DOI: 10.1021/Acs.Inorgchem.7B00392  0.533
2017 Glover SD, Parada GA, Markle TF, Ott S, Hammarström L. Isolating the Effects of the Proton Tunneling Distance on Proton-Coupled Electron Transfer in a Series of Homologous Tyrosine-Base Model Compounds. Journal of the American Chemical Society. PMID 28052668 DOI: 10.1021/Jacs.6B12531  0.681
2016 Schlotthauer T, Suchland B, Görls H, Parada GA, Hammarström L, Schubert US, Jäger M. Aryl-Decorated Ru(II) Polypyridyl-type Photosensitizer Approaching NIR Emission with Microsecond Excited State Lifetimes. Inorganic Chemistry. PMID 27228222 DOI: 10.1021/Acs.Inorgchem.6B00420  0.538
2015 Parada GA, Markle TF, Glover SD, Hammarström L, Ott S, Zietz B. Control over excited state intramolecular proton transfer and photoinduced tautomerization: influence of the hydrogen-bond geometry. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 6362-6. PMID 25728475 DOI: 10.1002/Chem.201500244  0.683
2013 Parada GA, Fredin LA, Santoni MP, Jäger M, Lomoth R, Hammarström L, Johansson O, Persson P, Ott S. Tuning the electronics of bis(tridentate)ruthenium(II) complexes with long-lived excited states: modifications to the ligand skeleton beyond classical electron donor or electron withdrawing group decorations. Inorganic Chemistry. 52: 5128-37. PMID 23597274 DOI: 10.1021/Ic400009M  0.664
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