Frank McKay

ORCID: 0009-0009-5093-4753
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Research Areas
  • High Entropy Alloys Studies
  • 2D Materials and Applications
  • High-Temperature Coating Behaviors
  • Chalcogenide Semiconductor Thin Films
  • Chemical Synthesis and Analysis
  • Additive Manufacturing Materials and Processes
  • MXene and MAX Phase Materials
  • Metal and Thin Film Mechanics
  • Synthesis and pharmacology of benzodiazepine derivatives
  • Electron and X-Ray Spectroscopy Techniques
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Synthesis and biological activity
  • Advanced Thermoelectric Materials and Devices
  • Aluminum Alloy Microstructure Properties
  • High Temperature Alloys and Creep
  • Advanced Materials Characterization Techniques
  • Synthesis and Characterization of Heterocyclic Compounds
  • Advanced materials and composites
  • Synthesis and Biological Evaluation
  • Chemical Synthesis and Reactions
  • Oxidative Organic Chemistry Reactions
  • Asymmetric Synthesis and Catalysis

Louisiana State University
2021-2024

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTNew Amine-masking Groups for Peptide SynthesisFrank C. McKay and Noel F. AlbertsonCite this: J. Am. Chem. Soc. 1957, 79, 17, 4686–4690Publication Date (Print):September 1, 1957Publication History Published online1 May 2002Published inissue 1 September 1957https://pubs.acs.org/doi/10.1021/ja01574a029https://doi.org/10.1021/ja01574a029research-articleACS PublicationsRequest reuse permissionsArticle Views1452Altmetric-Citations234LEARN ABOUT THESE...

10.1021/ja01574a029 article EN Journal of the American Chemical Society 1957-09-01

High-entropy alloys (HEAs) have intriguing material properties, but their potential as catalysts has not been widely explored. Based on a concise theoretical model, we predict that the surface of quaternary HEA base metals, CoCrFeNi, should go from being nearly fully oxidized except for pure Ni sites when exposed to O

10.1021/acs.jpcc.1c03646 article EN cc-by The Journal of Physical Chemistry C 2021-08-03

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTAcid-catalyzed DecarbobenzoxylationNoel F. Albertson and Frank C. McKayCite this: J. Am. Chem. Soc. 1953, 75, 21, 5323–5326Publication Date (Print):November 1, 1953Publication History Published online1 May 2002Published inissue 1 November 1953https://pubs.acs.org/doi/10.1021/ja01117a053https://doi.org/10.1021/ja01117a053research-articleACS PublicationsRequest reuse permissionsArticle Views145Altmetric-Citations35LEARN ABOUT THESE METRICSArticle...

10.1021/ja01117a053 article EN Journal of the American Chemical Society 1953-11-01

As new alloys are being developed for additive manufacturing (AM) applications, questions related to the temperature-dependent structural and compositional stability of these remain. In this work, benefits limitations a unique method testing presented. This system employs use polychromatic synchrotron light perform energy-dispersive x-ray diffraction (ED-XRD) on an electrostatically levitated sample at high temperatures. comparison with traditional angular-dispersive setup, container-less...

10.1063/5.0213480 article EN Review of Scientific Instruments 2024-11-01

The vibrational properties of CO, O2, and H2 molecularly or dissociatively adsorbed on a CoCrFeNi(110) surface have been probed using high-resolution energy loss spectroscopy (HREELS) modeled density functional theory (DFT) calculations. Large (∼20 mm3) single-crystal, quaternary face-centered cubic CoCrFeNi was synthesized via modified Czochralski technique. We show strong evidence that CO adsorbs primarily bridge on-top sites in compositionally varied local environments, which reflect the...

10.1021/acs.jpcc.4c03938 article EN cc-by The Journal of Physical Chemistry C 2024-08-19

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSynthesis of some pentazocine metabolites and related compoundsNoel F. Albertson Frank C. McKayCite this: J. Med. Chem. 1977, 20, 4, 602–604Publication Date (Print):April 1, 1977Publication History Published online1 May 2002Published inissue 1 April 1977https://pubs.acs.org/doi/10.1021/jm00214a036https://doi.org/10.1021/jm00214a036research-articleACS PublicationsRequest reuse permissionsArticle Views158Altmetric-Citations4LEARN ABOUT THESE...

10.1021/jm00214a036 article EN Journal of Medicinal Chemistry 1977-04-01

Abstract Chloracetaldehyd (I) liefert das sterisch einheitliche Olefin (II), zu (IIIa) substituiert wird.

10.1002/chin.197736260 article DE Chemischer Informationsdienst 1977-09-06
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