Grover W. Everett
Chancellors Club Teaching Professor, 1994-1999
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Academic Degrees
- B.S., 1962, University of North Carolina
- Ph.D., 1966, Harvard University
Research Interests
Professor Everett retired in 1999 after 33 years at KU. During this period he took four sabbatical leaves, one to England and three to Australia. Much of his research focused on various applications of nuclear magnetic resonance spectroscopy (1H, 2H, 13C, 59Co, 15N, 31P, 19F) to study coordination compounds of transition metals and to reveal binding sites of cations on biological ionophores. Nmr isotropic shifts and spin-lattice relaxation times were used to establish solution structures of compounds containing paramagnetic ions. He was one of the first to show the advantage of deuteron nmr for studying paramagnetic compounds. Other interests included investigations of stereoselectivity, stereoisomerization (thermal, photochemical, and electrochemical), and determination of absolute configurations of chiral complexes using circular dichroism and crystallographic techniques. He also studied reactions of coordinated ligands, membrane ion transport by ionophores, and enzyme-substrate interactions (in collaboration with Professor Himes in the Department of Biochemistry).
Since retiring, Professor Everett has been avidly studying geology, astronomy, meteorology, physics, biology, and Spanish.
Representative Publications
C.R. Powers and G.W. Everett, Jr., “The Stereochemistry and Proton Resonance Study of Bis[3-(N-substituted-amino)methylenecamphorato]nickel(II) Complexes,” J. Amer. Chem. Soc., 1969, 91, 3468 – 3476.
R.M. King and G.W. Everett, Jr., “Stereoselectivity in Octahedral Complexes IV. Separation and Identification of the Diastereomers of Tris[(+)-3-acetylcamphorato]Cobalt(III) and –Chromium(III),” Inorg. Chem., 1971, 10, 1237 – 1241.
R.R. Horn and G.W. Everett, Jr., “Proton and Deuteron Nuclear Magnetic Resonance Isotope Shifts in Partially Deuterated Tris[2,4-pentanedionato)vanadium(III),” J. Amer. Chem. Soc., 1971, 93, 7173 – 7178.
A. Johnson and G.W. Everett, Jr., “A Comparison of Proton and Deuteron Nuclear Magnetic Resonance of Some Paramagnetic Transition-Metal Complexes,” J. Amer. Chem. Soc., 1972, 94, 1419 – 1425.
G.W. Everett, Jr. and R.R. Horn, “Electrochemistry and Isomerization Kinetics of Tris[(+)-3-acetylcamphorato]ruthenium(III). Circular Dichroism and Absolute Configurations of the Analogous Ruthenium(II) and Ruthenium(IV) Diastereomers,” J. Amer. Chem. Soc., 1974, 96, 2087 – 2094.
S.A. Brawner, I.J.B. Lin, J.H. Kim, and G.W. Everett, Jr., “Synthesis of Beta-Diiminate Chelates by Condensation of 2,4-Pentanedione with Pt(NH3)6Cl4, Pt(en)3Cl4, and Au(en)2Cl3. Crystal and Molecular Structure of Trans[Pt(NH3)2(2,4-pentanediiminate)2](ClO4)2,” Inorg. Chem., 1978, 17, 1304 – 1308.
J.H. Kim and G.W. Everett, Jr., “Crystal and Molecular Structure of a Macrocyclic Complex of Gold(III),” Inorg. Chem., 1981, 20, 853 – 856.
J.Y. Lee and G.W. Everett, Jr., “Binding of Manganese(II) by Tetracycline. A Carbon-13 NMR Spin-Lattice Relaxation Study,” J. Amer. Chem. Soc., 1981, 103, 5221 – 5225.
D.A. Hanna, C. Yeh, J. Shaw, and G.W. Everett, Jr., “Gadolinium(III) and Manganese(II) Binding by a Polyether Ionophore. Influence of Cation Charge and Solvent Polarity on the Binding Sites of Lasalocid A (X-537A),” Biochemistry, 1983, 22, 5619 – 5626.
M.F. Wendland, T.H. Stevens, D.H. Buttlaire, G.W. Everett, Jr., and R.H. Himes, “Nuclear Magnetic Resonance Studies of Formyltetrahydrofolate Synthetase Interactions with Formate and Methylammonium Ion,” Biochemistry, 1983, 22, 819 – 826.
C. Yeh, D.A. Hanna, G.W. Everett, Jr., and R.H. Himes, “Nuclear Magnetic Resonance Relaxation Studies of the Interaction of Ligands with the Monomer and Tetramer Forms of Formyltetrahydrafolate Synthetase,” Biochemical Journal, 1988, 251, 89 – 93.
P.S.K. Chia, L.F. Lindoy, G.W. Walker, and G.W. Everett, Jr., “Supramolecular Transport of Metal Ammine and Amine Complexes Through Chloroform Membranes by the Natural Ionophore, Lasalocid A. The Selective Enantiomeric Transport of Chiral Metal Complexes, “ J. Amer. Chem. Soc., 1991, 113, 2533 – 2537.





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