scholarly journals Formation of an Unusual Four-Membered Nitrogen Ring (Tetrazetidine) Radical Cation

2012 ◽  
Vol 134 (39) ◽  
pp. 16188-16196 ◽  
Author(s):  
David Camp ◽  
Marc Campitelli ◽  
Graeme R. Hanson ◽  
Ian D. Jenkins
Keyword(s):  
Radical Cation ◽  
Nitrogen Ring

The electronic properties of a radical cation salt of bis-ethylenedioxodibenzofuran, [(bEDODBF)5 (AsF6)2(CH2Cl 2)0.2]

1988 ◽  
Vol 49 (4) ◽  
pp. 667-673 ◽  
Author(s):  
S. Söderholm ◽  
J. Hellberg ◽  
G. Ahlgren ◽  
M. Krebs ◽  
J.U. von Schütz ◽  
...  
Keyword(s):  
Electronic Properties ◽  
Radical Cation ◽  
Radical Cation Salt

Effects of Ultrasounds on Neat nitrobenzene

2019 ◽  
Vol 70 (8) ◽  
pp. 3085-3088
Author(s):  
Carmen Eugenia Stavarache ◽  
Yasuaki Maeda ◽  
Mircea Vinatoru
Keyword(s):  
Nitro Group ◽  
Radical Cation ◽  
Reaction Mechanisms ◽  
Diphenyl Ether ◽  
Argon Atmosphere ◽  
Phenyl Radical ◽  
Dissolved Gas ◽  
Decomposition Products ◽  
Oxygenated Compounds ◽  
Phenyl Cation

Neat nitrobenzene was continuously irradiated at two ultrasonic frequencies: 40 and 200 kHz, under air and argon atmosphere, respectively. Samples taken at intervals of 1, 5, 10 and 24 h were analyzed by GC-MS and decomposition products were identified. Possible reaction mechanisms are discussed. Presence of air as dissolved gas leads to oxygenated compounds such as 1,4-benzoquinone, 2,4-dinitrophenol, m-dinitrobenzene while argon inhibits the decomposition of nitrobenzene, especially at sonication times under 5 h. Based on the nature of the compounds identified we advanced a mechanism, involving a divergent splitting of unstable radical cation of NB in air and argon respectively. Thus, under air, the phenyl cation formation is preferred leading to 1,4-benzoquinone nitro-biphenyls and dinitrobenzene, while under argon, the phenyl radical formation seems to be favored, leading to phenol and diphenyl ether. The oxygenated compounds detected under argon clearly are a consequence of the nitro group splitting.

Structure of tetramethylsilane radical cation: an ESR and theoretical study

1991 ◽  
Vol 95 (8) ◽  
pp. 3132-3135 ◽  
Author(s):  
L. Bonazzola ◽  
J. P. Michaut ◽  
J. Roncin
Keyword(s):  
Radical Cation ◽  
Theoretical Study

scholarly journals New Radical Cation Salts Based on BDH-TTP Donor: Two Stable Molecular Metals with a Magnetic [ReF6]2− Anion and a Semiconductor with a [ReO4]− Anion

2021 ◽  
Vol 7 (4) ◽  
pp. 54
Author(s):  
Nataliya D. Kushch ◽  
Gennady V. Shilov ◽  
Lev I. Buravov ◽  
Eduard B. Yagubskii ◽  
Vladimir N. Zverev ◽  
...  
Keyword(s):  
Radical Cation ◽  
Low Temperatures ◽  
Ac Susceptibility ◽  
Slow Relaxation ◽  
Organic Radical ◽  
Inorganic Anion ◽  
Distinctive Features ◽  
Metallic Character ◽  
Radical Cation Salts ◽  
Partial Population

Three radical cation salts of BDH-TTP with the paramagnetic [ReF6]2− and diamagnetic [ReO4]− anions have been synthesized: κ-(BDH-TTP)4ReF6 (1), κ-(BDH-TTP)4ReF6·4.8H2O (2) and pseudo-κ″-(BDH-TTP)3(ReO4)2 (3). The crystal and band structures, as well as the conducting properties of the salts, have been studied. The structures of the three salts are layered and characterized by alternating κ-(1, 2) and κ″-(3) type organic radical cation layers with inorganic anion sheets. Similar to other κ-salts, the conducting layers in the crystals of 1 and 2 are formed by BDH-TTP dimers. The partial population of positions of Re atoms and disorder in the anionic layers of 1–3 are their distinctive features. Compounds 1 and 2 show the metallic character of conductivity down to low temperatures, while 3 is a semiconductor. The ac susceptibility of crystals 1 was investigated in order to test the possible slow relaxation of magnetization associated with the [ReF6]2− anion.

Electron n-doping of a highly electron-deficient chlorinated benzodifurandione-based oligophenylene vinylene polymer using benzyl viologen radical cations

2021 ◽  
Author(s):  
Teck Lip Dexter Tam ◽  
Albertus Denny Handoko ◽  
Ting Ting Lin ◽  
Jianwei Xu
Keyword(s):  
Radical Cation ◽  
Radical Cations ◽  
Benzyl Viologen ◽  
Electron Doping ◽  
N Doping ◽  
Polyphenylene Vinylene

Successful electron-doping of highly electron-deficient chlorinated benzodifurandione-based polyphenylene vinylene using viologen radical cation.

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