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William D. Jones
Researcher at University of Rochester
Publications - 318
Citations - 14914
William D. Jones is an academic researcher from University of Rochester. The author has contributed to research in topics: Catalysis & Oxidative addition. The author has an hindex of 68, co-authored 314 publications receiving 13989 citations. Previous affiliations of William D. Jones include University of Wisconsin-Madison & University of Rochester Medical Center.
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Journal ArticleDOI
Rapid oxidative hydrogen evolution from a family of square-planar nickel hydride complexes
Srinivasan Ramakrishnan,Sumit Chakraborty,William W. Brennessel,Christopher E. D. Chidsey,William D. Jones +4 more
TL;DR: A series of square-planar nickel hydride complexes supported by bis(phosphinite) pincer ligands with varying substituents (OMe, Me, and But) on the pincers backbone have been synthesized and completely characterized by NMR spectroscopy, IR and X-ray crystallography as mentioned in this paper.
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Organometallics Roundtable 2011
John A. Gladysz,Zachary T. Ball,Guy Bertrand,Suzanne A. Blum,Vy M. Dong,Reto Dorta,Reto Dorta,F. Ekkehardt Hahn,Mark G. Humphrey,William D. Jones,Jerzy Klosin,Ian Manners,Tobin J. Marks,James M. Mayer,Bernhard Rieger,Joachim C. Ritter,Alfred P. Sattelberger,Jennifer M. Schomaker,Vivian Wing-Wah Yam +18 more
TL;DR: A panel of seventeen experts who share their thoughts on a variety of matters of importance to our field was assembled by Organometallics in 2011 as discussed by the authors, where an attempt was made to secure representation from a number of countries and career stages.
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Chemical and electrochemical oxidation of CpRe(PAr3)2H2 complexes to give stable 17-electron radical cations. Disproportionation to diamagnetic species via electron-transfer catalysis
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Synthesis and X-ray crystallographic characterization of substituted aryl imines
TL;DR: In this article, the synthesis of α-diimine 1,4-bis(2,5-di-tert-butylphenyl)-2,3-dimethyl-1, 4-diaza 1, 3-butadiene, 1, and α-iminoketones 2-[(3, 5-xylyl)imino]acenaphthylen-1-one, 4, and 2]-(4-chlorophenyl)IMino]acetyln-enaphthene, 5, all
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P−C Bond Scission at the TRIPHOS Ligand and C−CN Bond Cleavage in 2-Methyl-3-butenenitrile with [Ni(COD)2]
TL;DR: The use of catalytic amounts of [Ni(COD)2] and TRIPHOS (bis(2-diphenylphosphinoethyl)phenylphophosphine) allowed the isomerization of 2-methyl-3-butenenitrile (2M3BN) at 100 °C, to yield Z- and E-2-methyl 2-butensynitrile(2M2BN) as mentioned in this paper.