Relevant bibliographies by topics / Super-Electron-Donor

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  1. Journal articles

Academic literature on the topic 'Super-Electron-Donor'

Author: Grafiati
Published: 4 June 2025
Last updated: 15 July 2025

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Journal articles on the topic "Super-Electron-Donor"

1

Nozawa-Kumada, Kanako, Shungo Ito, Koto Noguchi, Masanori Shigeno, and Yoshinori Kondo. "Super electron donor-mediated reductive desulfurization reactions." Chemical Communications 55, no. 86 (2019): 12968–71. http://dx.doi.org/10.1039/c9cc06775b.

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2

Panetti, Grace B., Patrick J. Carroll, Michael R. Gau, Brian C. Manor, Eric J. Schelter, and Patrick J. Walsh. "Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions." Chemical Science 12, no. 12 (2021): 4405–10. http://dx.doi.org/10.1039/d0sc04822d.

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The super electron donor (SED) capabilities of 2-azaallyl anions has recently been discovered and applied to diverse reactivity; their structures and electron transfer characteristics are reported herein.
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3

Nozawa-Kumada, Kanako, Erina Abe, Shungo Ito, Masanori Shigeno, and Yoshinori Kondo. "Super electron donor-mediated reductive transformation of nitrobenzenes: a novel strategy to synthesize azobenzenes and phenazines." Organic & Biomolecular Chemistry 16, no. 17 (2018): 3095–98. http://dx.doi.org/10.1039/c8ob00271a.

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4

Garnier, Jean, Douglas W. Thomson, Shengze Zhou, Phillip I. Jolly, Leonard E. A. Berlouis, and John A. Murphy. "Hybrid super electron donors – preparation and reactivity." Beilstein Journal of Organic Chemistry 8 (July 3, 2012): 994–1002. http://dx.doi.org/10.3762/bjoc.8.112.

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Neutral organic electron donors, featuring pyridinylidene–imidazolylidene, pyridinylidene–benzimidazolylidene and imidazolylidene–benzimidazolylidene linkages are reported. The pyridinylidene–benzimidazolylidene and imidazolylidene–benzimidazolylidene hybrid systems were designed to be the first super electron donors to convert iodoarenes to aryl radicals at room temperature, and indeed both show evidence for significant aryl radical formation at room temperature. The stronger pyridinylidene–imidazolylidene donor converts iodoarenes to aryl anions efficiently under appropriate conditions (3 equiv of donor). The presence of excess sodium hydride base has a very important and selective effect on some of these electron-transfer reactions, and a rationale for this is proposed.
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5

Zi, Quanxing, Minyan Li, Jielun Cong, et al. "Super-Electron-Donor 2-Azaallyl Anions Enable Construction of Isoquinolines." Organic Letters 24, no. 9 (2022): 1786–90. http://dx.doi.org/10.1021/acs.orglett.2c00140.

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6

Vaid, Thomas P., and Melanie S. Sanford. "An organic super-electron-donor as a high energy density negative electrolyte for nonaqueous flow batteries." Chemical Communications 55, no. 74 (2019): 11037–40. http://dx.doi.org/10.1039/c9cc06080d.

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An organic “super-electron-donor” is well-suited as a negative electrolyte for nonaqueous redox flow batteries, with a highly negative 2<sup>+</sup>/0 reduction potential, a low mass per electron stored, and good solubility in CH<sub>3</sub>CN in both redox states.
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7

Humphries, Matthew E., Emily S. Wusterbarth, and Dennis L. Lichtenberger. "Weak acids with super-electron-donor dimetal complexes: Synergy in bifunctional activity." Polyhedron 158 (January 2019): 471–77. http://dx.doi.org/10.1016/j.poly.2018.11.001.

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8

Cumine, Florimond, Fabrizio Palumbo, and John A. Murphy. "Reduction of nitroarenes, azoarenes and hydrazine derivatives by an organic super electron donor." Tetrahedron 74, no. 38 (2018): 5539–45. http://dx.doi.org/10.1016/j.tet.2018.04.069.

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9

Jolly, Phillip I., Nadia Fleary-Roberts, Steven O'Sullivan, Eswararao Doni, Shengze Zhou, and John A. Murphy. "Reactions of triflate esters and triflamides with an organic neutral super-electron-donor." Organic & Biomolecular Chemistry 10, no. 30 (2012): 5807. http://dx.doi.org/10.1039/c2ob25116g.

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10

Schoenebeck, Franziska, John A. Murphy, Sheng-ze Zhou, Yoshitaka Uenoyama, Yves Miclo, and Tell Tuttle. "Reductive Cleavage of Sulfones and Sulfonamides by a Neutral Organic Super-Electron-Donor (S.E.D.) Reagent." Journal of the American Chemical Society 129, no. 44 (2007): 13368–69. http://dx.doi.org/10.1021/ja074417h.

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