Warren J. Oldham

ORCID: 0000-0002-0997-2653
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Research Areas
  • Radioactive contamination and transfer
  • Radioactive element chemistry and processing
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Radioactivity and Radon Measurements
  • Nuclear Physics and Applications
  • Organic Light-Emitting Diodes Research
  • Nuclear reactor physics and engineering
  • Ionic liquids properties and applications
  • Nuclear Materials and Properties
  • Organic Electronics and Photovoltaics
  • Molecular Junctions and Nanostructures
  • Organometallic Complex Synthesis and Catalysis
  • Synthesis and Properties of Aromatic Compounds
  • Conducting polymers and applications
  • Radiopharmaceutical Chemistry and Applications
  • Luminescence and Fluorescent Materials
  • Electrochemical Analysis and Applications
  • Nuclear and radioactivity studies
  • Chemical Synthesis and Characterization
  • Coordination Chemistry and Organometallics
  • Molten salt chemistry and electrochemical processes
  • Molecular spectroscopy and chirality
  • Lichen and fungal ecology
  • Crystallography and molecular interactions

Los Alamos National Laboratory
2010-2023

University of Cincinnati
2003

University of Rochester
1998-2001

University of Washington
1996-2000

University of California, Santa Barbara
1998-2000

National Iranian Oil Company (Iran)
1947

A novel topological strategy is described for designing amorphous molecular solids suitable optoelectronic applications. In this approach, chromophores are attached to a tetrahdral point of convergence. Stilbenoid units were covalently linked tetraphenylmethane, tetraphenyladamantane, or tetraphenylsilane cores using palladium catalyzed coupling methodology. Thus, reaction E(C6H5X)4 (E = C and adamantane, X I; E Si, Br) with styrene 4,4'-tert-butylvinylstilbene under Heck conditions yields...

10.1021/ja992924w article EN Journal of the American Chemical Society 2000-06-01

A series of paracyclophane derivatives that hold chromophores varying conjugation lengths has been synthesized using palladium-mediated coupling reactions. These molecules mimic solid-state interactions in main-chain polychromophores and conjugated emissive polymers such as poly(p-phenylenevinylene) (PPV). Their optical properties give insight into the energetics photoexcitations localized a discrete chromophore relative to state containing through-space delocalized core. Thus,...

10.1021/ja973816h article EN Journal of the American Chemical Society 1998-08-29

Protonation of TpM(PR3)H2 (M = Rh, Ir) complexes with HBF4·Et2O or [H(Et2O)2][B(Ar)4] (Ar 3,5-(CF3)2C6H3) affords cationic which exhibit a single hydride resonance at all accessible temperatures in the 1H NMR spectrum. Formulation as fluxional dihydrogen/hydride is indicated by short T1(min) values ca. 22 ms (Ir) and 7 (Rh). The relaxation times are consistent H−H bond lengths 0.88−1.11 Å iridium 0.73−0.92 rhodium depending on relative rate dihydrogen rotational motion. In case complexes,...

10.1021/ja971627t article EN Journal of the American Chemical Society 1997-11-01

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTSynthesis, Spectroscopy, and Morphology of TetrastilbenoidmethanesWarren J. Oldham, Jr.†, Rene Lachicotte, Guillermo C. Bazan*View Author Information Department Chemistry, University Rochester Rochester, New York 14627 † Current address: FED Corporation, Hopewell Junction, NY 12533. In papers with more than one author, the asterisk indicates name author to whom inquiries about paper should be addressed.Cite this: Am. Chem. Soc. 1998, 120, 12,...

10.1021/ja974209x article EN Journal of the American Chemical Society 1998-03-17

Treatment of UO2Cl2(thf)3 in THF with two equivalents 1,3-dimesitylimidazole-2-ylidene (IMes) or 1,3-dimesityl-4,5-dichloroimidazole-2-ylidene (IMesCl2) yields novel monomeric uranyl N-heterocyclic carbene complexes, representing the first examples actinyl carbon bonds.

10.1039/b102649f article EN Chemical Communications 2001-01-01

This paper describes an approach to measuring extinct fission products that would allow for the characterization of a nuclear test at any time. The isotopic composition molybdenum in five samples glassy debris from 1945 Trinity has been measured. Nonnatural compositions were observed, reflecting input decay short-lived (95)Zr and (97)Zr. By both perturbation (95)Mo/(96)Mo (97)Mo/(96)Mo ratios total amount samples, it is possible calculate original concentrations (97)Zr isotopes formed...

10.1073/pnas.1602792113 article EN Proceedings of the National Academy of Sciences 2016-07-05

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPreparation and Properties of [TpIr(PMe3)(H2)H]BF4: observation Novel Isotopic PerturbationD. M. Heinekey Warren J. Oldham Jr.Cite this: Am. Chem. Soc. 1994, 116, 7, 3137–3138Publication Date (Print):April 1, 1994Publication History Published online1 May 2002Published inissue 1 April 1994https://pubs.acs.org/doi/10.1021/ja00086a059https://doi.org/10.1021/ja00086a059research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ja00086a059 article EN Journal of the American Chemical Society 1994-04-01

Room temperature ionic liquids composed of bis(trifluoromethylsulfonyl)imide anions and 1,3-ethylmethylimidazolium (EMI) cations are shown to stabilize monomeric ligand deficient transition metal complexes via four distinct binding modes: monodentate nitrogen or oxygen coordination and/or bidentate oxygen-oxygen' nitrogen-oxygen (eta1-N, eta1-O, eta2-O,O' eta2-N,O).

10.1039/b416830e article EN Chemical Communications 2005-01-01

Two pseudo-para substituted bis-diimino[2.2]paracyclophane ligands (4,16-bis(picolinaldimine)-[2.2]paracyclophane (BPPc) and 4,16-bis(methyl-picolinaldimine)-[2.2]paracyclophane (BmPPc)) were prepared by the condensation reaction of appropriate picolinaldimine with 4,16-diamino-[2.2]paracyclophane (2). An improved synthesis 2 from [2.2]paracyclophane also is reported. BPPc (3a): monoclinic, P2(1)/c, a = 8.2238(11) A, b 15.336(2) c 8.4532(11) beta 98.578(3) degrees, V 1054.2(2) A(3), Z 2. To...

10.1021/ic0348648 article EN Inorganic Chemistry 2003-12-13

As part of a nuclear forensics capability, rapid and effective methods to analyze for plutonium other actinide metals are needed. A key requirement these is that they afford high chemical yield while still providing isotopic information necessary forensic evaluation. Toward this objective, new method binding analysis by alpha spectrometry has been developed. Thin films Kläui-type tripodal oxygen donor ligands were prepared spin-casting solutions onto glass substrates. Three different...

10.1021/ac402997e article EN Analytical Chemistry 2014-01-07

Solutions of TpM(C2H4)2 (M = Rh (1a) and Ir (1b)) react with 1 equiv PPh3 to yield TpM(PPh3)(C2H4) (2a,b). The new complexes adopt trigonal-bipyramidal structures in solution triphenylphosphine coordinated the axial site ethylene positioned equatorial plane. For 2a pyrazolyl arms Tp ligand exchange positions on NMR time scale (ΔG⧧ 14.3 kcal mol-1, 279 K); however, no is observed case 2b, even at 353 K > 18.4 mol-1). Complexes 2a,b molecular hydrogen TpM(PPh3)H2 (3a,b) free ethylene. Kinetic...

10.1021/om9605140 article EN Organometallics 1997-02-01

New measurement and assessment techniques have been applied to the radiochemical reevaluation of Trinity Event. Thirteen trinitite samples were dissolved analyzed using a combination traditional decay counting methods mass spectrometry techniques. The resulting data assessed advanced simulation tools afford final yield determination 24.8 ± 2 kt TNT equivalent, substantially higher than previous U.S. Department Energy released value 21 kt.

10.1080/00295450.2021.1932176 article EN cc-by-nc-nd Nuclear Technology 2021-11-16

S. F. Birch, W. J. Oldham and E. A. Johnson, Chem. Soc., 1947, 818 DOI: 10.1039/JR9470000818

10.1039/jr9470000818 article EN Journal of the Chemical Society (Resumed) 1947-01-01

In nuclear forensic analyses, measurements of actinide elements in a sample can assist with identifying interdicted or unknown materials. While these radiochemical signatures have been extensively investigated uranium materials, less is known about bulk neptunium samples. This paper describes the measurement trace concentrations and isotopic profiles 237Np oxide sample. Uranium, plutonium, americium, curium were determined deemed potentially useful for distinguishing different sources 237Np....

10.1021/acs.analchem.3c01682 article EN Analytical Chemistry 2023-06-01

Abstract The N‐heterocyclic carbene, 1,3‐dimesityl‐imidazol‐2‐ylidene (IMes) reacts with tetrahydrofuran (THF) in the presence of an oxidizing uranyl triflate complex, UO 2 (OTf) (thf) 3 ( − OTf = OSO CF ), to give 1,4‐bis(1,3‐dimesityl‐2‐imidazolium)‐1,3‐butadiene bis(trifluoromethanesulfonate), formally understood as coupling product two equivalents IMes [CHCHCHCH](OTf) . Copyright © 2005 John Wiley & Sons, Ltd.

10.1002/aoc.1008 article EN Applied Organometallic Chemistry 2005-11-16

On July 16, 1945, the Trinity nuclear test exploded in desert near Alamogordo, New Mexico. A variety of new diagnostic experiments were fielded an effort to understand detailed performance device. This paper describes a series radiochemical that designed measure efficiency and neutron fluence test. These experiments, scientists who led them, laid foundation weapons radiochemistry for decades come.

10.1080/00295450.2021.1951538 article EN cc-by-nc-nd Nuclear Technology 2021-11-16

Nanosecond electroluminescence (EL) overshoots observed when multilayer blue 4,4′-bis(2,2′-diphenyl vinyl)-1,1′-biphenyl (DPVBi)-based organic light-emitting devices (OLEDs) are excited by rectangular voltage pulses described. The occur at the turn-off and exceed cw brightness up to an order of magnitude. Time-resolved images OLEDs demonstrate that emission from most sample surface decays with a single time constant τ1=13±3 ns. This decay is attributed recombination charges which accumulate...

10.1063/1.126076 article EN Applied Physics Letters 2000-03-20

Methylene chloride solutions of the tris(1-pyrazolyl)borate (Tp) complexes TpIr(PPh3)(C2H4) or TpIr(C2H4)2 react with excess PPh3 via activation a pyrazole C−H bond to form equilibrium mixtures TpIr(PPh3)(C2H4), (N,C5,N-Tp-H)Ir(PPh3)2H (1), and free ethylene upon standing at room temperature. Complete conversion 1 was accomplished by removing displaced ethylene. The hydride complex purified protonation unbound nitrogen ring afford cationic 2 as BF4 salt. Deprotonation affords in good yield...

10.1021/om990720i article EN Organometallics 2000-03-28
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