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Michael M. Haley

University of Oregon, Eugene, OR, United States 
Organic, Organometallic, & Materials Chemistry
"Michael Haley"
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Sherbow TJ, Fargher HA, Haley MM, et al. (2020) Solvent-Dependent Linear Free Energy Relationship in a Flexible Host-Guest System. The Journal of Organic Chemistry
Dressler J, Barker JE, Karas LJ, et al. (2020) Late-stage Modification of Electronic Properties of Antiaromatic and Diradicaloid Indeno[1,2-b]fluorene Analogues via Sulfur Oxidation. The Journal of Organic Chemistry
Fargher HA, Lau N, Richardson HC, et al. (2020) Tuning Supramolecular Selectivity for Hydrosulfide: Linear Free Energy Relationships Reveal Preferential C-H Hydrogen Bond Interactions. Journal of the American Chemical Society
Nojo W, Reingold ID, Bard JP, et al. (2019) Donor-/Acceptor-Substituted Tetrakis(arylethynyl)benzenes: The Influence of Donor Group on Optoelectronic Properties. Chempluschem. 84: 1391-1395
Barker JE, Kodama T, Song MK, et al. (2019) Serendipitous Rediscovery of the Facile Cyclization of Z,Z-3,5-Octadiene-1,7-diyne Derivatives to Afford Stable, Substituted Naphthocyclobutadienes. Chempluschem. 84: 665-672
Barker JE, Dressler JJ, Cárdenas Valdivia A, et al. (2019) Molecule Isomerism Modulates the Diradical Properties of Stable Singlet Diradicaloids. Journal of the American Chemical Society
Bard JP, Bates HJ, Deng CL, et al. (2019) Amplification of the Quantum Yields of 2-λ-Phosphaquinolin-2-ones Through Phosphorus Center Modification. The Journal of Organic Chemistry
Deng CL, Bard JP, Zakharov LN, et al. (2019) PN-Containing Pyrene Derivatives: Synthesis, Structure, and Photophysical Properties. Organic Letters
Deng CL, Bard JP, Zakharov LN, et al. (2019) Naphtho[2,1- e]-1,2-azaphosphorine-2-oxide Derivatives: Synthesis, Optoelectronic Properties, and Self-Dimerization Phenomena. The Journal of Organic Chemistry
Eytel LM, Fargher HA, Haley MM, et al. (2019) The road to aryl CHanion binding was paved with good intentions: fundamental studies, host design, and historical perspectives in CH hydrogen bonding. Chemical Communications (Cambridge, England)
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