Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Todd F. Markle"'
Publikováno v:
Journal of the American Chemical Society. 139:2090-2101
The distance dependence of concerted proton-coupled electron transfer (PCET) reactions was probed in a series of three new compounds, where a phenol is covalently bridged by a 5, 6, or 7 membered carbocycle to the quinoline. The carbocycle bridge enf
Publikováno v:
Chemical Science
Kinetic studies of the reactions of two previously characterized copper(III)-hydroxide complexes with a series of para substituted phenols (XArOH where X = NMe2, OMe, Me, H, Cl, NO2, or CF3) indicate competition between concerted CPET and sequential
Autor:
Giovanny A. Parada, Sascha Ott, Todd F. Markle, Burkhard Zietz, Leif Hammarström, Starla D. Glover
Publikováno v:
Chemistry - A European Journal. 21:6362-6366
The influence of H-bond geometry on the dynamics of excited state intramolecular proton transfer (ESIPT) and photoinduced tautomerization in a series of phenol-quinoline compounds is investigated. Control over the proton donor-acceptor distance (dDA
Publikováno v:
The Journal of Physical Chemistry A. 116:12249-12259
Separated concerted proton-electron transfer (sCPET) reactions of two series of phenols with pendent substituted pyridyl moieties are described. The pyridine is either attached directly to the phenol (HOAr-pyX) or connected through a methylene linker
Autor:
Todd F. Markle, James M. Mayer, Virginia W. Manner, Elizabeth A. Mader, James A. Franz, Adam Wu
Publikováno v:
Journal of the American Chemical Society. 131:4335-4345
Reported herein are thermochemical studies of hydrogen atom transfer (HAT) reactions involving transition metal H-atom donors M(II)LH and oxyl radicals. [Fe(II)(H(2)bip)(3)](2+), [Fe(II)(H(2)bim)(3)](2+), [Co(II)(H(2)bim)(3)](2+), and Ru(II)(acac)(2)
Publikováno v:
Proceedings of the National Academy of Sciences. 105:8185-8190
A series of seven substituted 4,6-di- tert -butyl-2-(4,5-diarylimidazolyl)-phenols have been prepared and characterized, along with two related benzimidazole compounds. X-ray crystal structures of all of the compounds show that the phenol and imidazo
Autor:
Ming-Tian Zhang, Todd F. Markle, Linus O. Johannissen, Leif Hammarström, Marie Pierre Santoni
Publikováno v:
Markle, T F, Zhang, M T, Santoni, M P, Johannissen, L O & Hammarström, L 2016, ' Proton-coupled electron transfer in a series of ruthenium-linked tyrosines with internal bases : Evaluation of a tunneling model for experimental temperature-dependent kinetics ', Journal of Physical Chemistry B, vol. 120, no. 35, pp. 9308-9321 . https://doi.org/10.1021/acs.jpcb.6b05885
Photoinitiated proton-coupled electron transfer (PCET) kinetics has been investigated in a series of four modified tyrosines linked to a ruthenium photosensitizer in acetonitrile, with each tyrosine bearing an internal hydrogen bond to a covalently l
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http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-305468
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-305468
Autor:
Todd F. Markle, Mark A. Lockwood, Antonio G. DiPasquale, Ian J. Rhile, Hirotaka Nagao, James M. Mayer, Katrina Rotter, Oanh P. Lam
Publikováno v:
Journal of the American Chemical Society. 128:6075-6088
Three phenols with pendant, hydrogen-bonded bases (HOAr-B) have been oxidized in MeCN with various one-electron oxidants. The bases are a primary amine (-CPh(2)NH(2)), an imidazole, and a pyridine. The product of chemical and quasi-reversible electro
Autor:
Antonio G. DiPasquale, Frank Bartnik Larsen, Ian J. Rhile, Elizabeth A. Mader, Todd F. Markle, James M. Mayer
Publikováno v:
Mayer, J M, Rhile, I J, Larsen, F B, Mader, E A, Markle, T F & DiPasquale, A G 2006, ' Models for proton-coupled electron transfer in photosystem II ', Photosynthesis Research, vol. 87, no. 1, pp. 3-20 .
The coupling of proton and electron transfers is a key part of the chemistry of photosynthesis. The oxidative side of photosystem II (PS II) in particular seems to involve a number of proton-coupled electron transfer (PCET) steps in the S-state trans
Autor:
Todd F. Markle, James M. Mayer
Publikováno v:
Angewandte Chemie International Edition. 47:738-740