Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Daniel Ess"'
Autor:
Arun K. Bhunia, Tao Geng, Angela Valadez, Aparna Kothapalli, Byoung-Kwon Hahm, Daniel Ess, Mark T. Morgan, Giyoung Kim, Viswaprakash Nanduri
Publikováno v:
Sensors, Vol 6, Iss 8, Pp 808-822 (2006)
Recent outbreaks of food borne illnesses continue to support the need for rapidand sensitive methods for detection of foodborne pathogens. A method for detecting Listeriamonocytogenes in food samples was developed using an automated fiber-optic-based
Externí odkaz:
https://doaj.org/article/9a3cf63ccfc24c2eb23e8399adb6aa31
Dinuclear metal complexes with a direct metal-metal interaction have the potential for unique mechanisms, intermediates, and selectivity during catalysis. Here we report density functional theory (DFT) calculations that directly evaluate the influenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3fb28752d6639f7dc6c3c7b27ae2448
https://doi.org/10.26434/chemrxiv-2023-v4b8f
https://doi.org/10.26434/chemrxiv-2023-v4b8f
Autor:
Jeong-Yu Son, Santeri Aikonen, Nathan Morgan, Alexander Harmata, Jesse Sabatini, Rosario Sausa, Edward Byrd, Daniel Ess, Robert Paton, Corey Stephenson
Cuneane is a strained hydrocarbon accessible via metal-catalyzed isomerization of cubane. The carbon atoms of cuneane define a polyhedron of the C2v point group with six faces- two triangular, two quadrilateral, and two pentagonal. The rigidity, stra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e08bc97863c5561818d34fcf9e371f5
https://doi.org/10.26434/chemrxiv-2023-0xn9c
https://doi.org/10.26434/chemrxiv-2023-0xn9c
Ni-catalyzed electrochemical aryl amination (e-amination) is an attractive, emerging approach to forging C−N bonds as it uses air-stable Ni catalysts and efficiently proceeds at room temperature. However, in-depth mechanistic understandings of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd6319a21422f97a60dd9f5c4ce24c7a
https://doi.org/10.26434/chemrxiv-2022-bpzwt
https://doi.org/10.26434/chemrxiv-2022-bpzwt
Autor:
Daniel Ess, Nathan Morgan, Steven Maley, Doo-Hyun Kwon, Michael Webster-Gardiner, Brooke Small, Orson Sydora, Steven Bischof
One approach to selectively generate 1-hexene is through ethylene trimerization using highly active Cr N-phosphinoamidine catalysts ((P,N)Cr). Depending on the ligand, (P,N)Cr catalysts can either generate nearly pure 1-hexene or form 1-hexene with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5ba64d9c50e4e1938a4a9dfaf43ca4a
https://doi.org/10.26434/chemrxiv-2021-brx24
https://doi.org/10.26434/chemrxiv-2021-brx24
Au and Pd complexes have emerged as highly effective π-bond cyclization catalysts to construct heterocycles. These cyclization reactions are generally proposed to proceed through multi-step addition-elimination mechanisms involving Au- or Pd-alkyl i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4e22d6156b25e16525a9a5291dacb46
https://doi.org/10.26434/chemrxiv.14700045
https://doi.org/10.26434/chemrxiv.14700045
Autor:
Matthew Asplund, Daniel Ess, David Michaelis, Michael R. Talley, Erin E. Martinez, Doo-Hyun Kwon, Jacob Davis, Kyle Clark
This work reports the synthesis of a triethylsilyl-substituted Fe-Cu complex that provided cyclohexane solubility to conduct time-resolved UV-IR studies. These studies suggest that UV light induces a photochemically active heterodinuclear species for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07f0e4695eefcf64cb037533b4617d9a
https://doi.org/10.26434/chemrxiv.14176646
https://doi.org/10.26434/chemrxiv.14176646
Autor:
Steven Maley, Doo-Hyun Kwon, Nick Rollins, Johnathan Stanley, Orson Sydora, Steven M. Bischof, Daniel Ess
The use of data science tools to provide the emergence of nontrivial chemical features for catalyst design is an important goal in catalysis science. Additionally, there is currently no general strategy for computational homogeneous, molecular cataly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::858d570066feb77d1634767971591c48
https://doi.org/10.26434/chemrxiv.12578552
https://doi.org/10.26434/chemrxiv.12578552
The synthesis and characterization of an iridium polyhydride complex (Ir-H4)supported by an electron-rich PCP framework is described. This complex readily loses molecularhydrogen allowing for rapid room temperature hydrogen isotope exchange (HIE) at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f704b2b47f6680584f9ab6bf5dc4983
https://doi.org/10.26434/chemrxiv.12276632.v1
https://doi.org/10.26434/chemrxiv.12276632.v1
The transfer of a -hydrogen from a metal-alkyl group to ethylene is a fundamentalorganometallic transformation. Previously proposed mechanisms for this transformation involve either atwo-step -hydrogen elimination and migratory insertion sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34c7161a24d53d5288c657af83c7abaa
https://doi.org/10.26434/chemrxiv.12156462.v1
https://doi.org/10.26434/chemrxiv.12156462.v1