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Publikováno v:
Applied Magnetic Resonance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::368be1f8fed0104d571e1e37e28973a2
https://doi.org/10.1007/s00723-021-01397-0
https://doi.org/10.1007/s00723-021-01397-0
Publikováno v:
Applied Magnetic Resonance. 54:359-370
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bf5a3e2e70a376df328df92240cc2da
https://doi.org/10.1007/s00723-022-01514-7
https://doi.org/10.1007/s00723-022-01514-7
Autor:
Gareth R. Eaton
Publikováno v:
Foundations of Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454106e41d7ad227204dcc402a48d7fe
https://doi.org/10.1007/s10698-023-09473-y
https://doi.org/10.1007/s10698-023-09473-y
Publikováno v:
Antioxidants & Redox Signaling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c35a83cb16b256721d851eb823b75ef5
https://doi.org/10.1089/ars.2022.0216
https://doi.org/10.1089/ars.2022.0216
Autor:
Cassidy E. Jackson, Thacien Ngendahimana, Chun-Yi Lin, Gareth R. Eaton, Sandra S. Eaton, Joseph M. Zadrozny
Publikováno v:
The Journal of Physical Chemistry C. 126:7169-7176
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac55e3e987c3df378888866b366a94a9
https://doi.org/10.1021/acs.jpcc.2c01090
https://doi.org/10.1021/acs.jpcc.2c01090
Autor:
Gareth R. Eaton
Publikováno v:
Foundations of Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f24f39221854d30e5d7a2242ab377af
https://doi.org/10.1007/s10698-023-09469-8
https://doi.org/10.1007/s10698-023-09469-8
Autor:
Martin Poncelet, Thacien Ngendahimana, Teresa D. Gluth, Emily H. Hoblitzell, Timothy D. Eubank, Gareth R. Eaton, Sandra S. Eaton, Benoit Driesschaert
Publikováno v:
The Analyst. 147:5643-5648
We report an isotopologue of the trityl radical OX071, labeled with 13C at the central carbon highly sensitive to molecular tumbling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25146eb89ed619325492e8757f34552b
https://doi.org/10.1039/d2an01527g
https://doi.org/10.1039/d2an01527g
Autor:
Shengdian Huang, Suchada Rajca, Gareth R. Eaton, Thacien Ngendahimana, Andrzej Rajca, Sandra S. Eaton, Maren Pink
Publikováno v:
The Journal of Organic Chemistry. 86:13636-13643
Synthesis of bis-spiro-oxetane and bis-spiro-tetrahydrofuran pyrroline nitroxide radicals relies on the Mitsunobu reaction-mediated double cyclizations of N-Boc protected pyrroline tetraols. Structures of the nitroxide radicals are supported by X-ray
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bde6f98d683a9b201d1ac470a620adad
https://doi.org/10.1021/acs.joc.1c01670
https://doi.org/10.1021/acs.joc.1c01670
Autor:
Eric A. Legenzov, Nathaniel D. A. Dirda, Joseph P. Y. Kao, Lukas B. Woodcock, Whylder Moore, Gareth R. Eaton, Sandra S. Eaton
Publikováno v:
Applied Magnetic Resonance. 53:221-232
EPR line shapes in fluid solution and electron spin relaxation times and lineshapes in frozen solution were measured at X-band for two dinitroxides. For dinitroxide 1, which has two proxyl nitroxides connected by an amide linkage, the fluid solution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5998c698919fa5885508d17a0b49d36b
https://doi.org/10.1007/s00723-021-01372-9
https://doi.org/10.1007/s00723-021-01372-9