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Creators/Authors contains: "Jones, William D"

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  1. ; ; (, Journal of Organometallic Chemistry)
    Free, publicly-accessible full text available November 1, 2026
  2. ; ; ; ; ; ; ; ; ; ; et al (, Soil Security)
    Free, publicly-accessible full text available June 1, 2026
  3. ; ; ; (, ACS Catalysis)
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  4. ; ; (, Chemistry)
    A single-step method for aniline formation was examined. Using a vanadate catalyst with an iron oxide co-catalyst and hydroxylamine hydrochloride as the amine source, an up to 90% yield of aniline was obtained with high selectivity. Further study showed that the overall reaction was pseudo-second order in terms of hydroxylamine concentration. Regioselective H-D exchange experiments suggest that the C-N bond formation step occurs via an irreversible electrophilic pathway. Based on all of the key observations, a mechanism is proposed. 
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  5. ; ; ; ; (, Inorganica Chimica Acta)
    Bipyridyl ligands are commonplace in catalysis. Structurally similar to this ligand class with unique properties is the novel di-(2-pyridyl)methanesulfonate (dpms) ligand, which is prepared and reacted with [Cp*IrCl2]2 to afford Cp*Ir(dpms)Cl (1) in high yield. Its single-crystal X-ray structure indicates an exo–(kappa2) conformation of the ligand, with the sulfonate group directed away from the iridium center. Halogen exchange by treatment of 1 with NaI gives the iodide derivative, Cp*Ir(dpms)I (2). Abstraction of the halogen from 1 using AgPF6 generates [Cp*Ir(dpms)]PF6 (3), which was not found to activate the C-H bonds of benzene. 
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  6. ; (, European Journal of Organic Chemistry)
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  7. ; ; ; (, Polyhedron)
    null (Ed.)
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  8. ; ; ; (, Polyhedron)
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  9. ; ; (, The Journal of Organic Chemistry)
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  10. ; ; ; (, Organometallics)