124774-74-9Relevant academic research and scientific papers
Dual dopable poly(phenylacetylene) with nitronyl nitroxide pendants for reversible ambipolar charging and discharging
Oyaizu, Kenichi,Sukegawa, Takashi,Nishide, Hiroyuki
, p. 184 - 185 (2011)
An electrode-attached layer of poly(phenylacetylene) bearing a pendant nitronyl nitroxide group per repeating unit, obtained by the Rh-catalyzed polymerization of 2-(4-ethynylphenyl)-4,4,5,5- tetramethylimidazoline-l-oxyl 3-oxide, underwent oxidation and
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
Petunin, Pavel V.,Rybalova, Tatyana V.,Trusova, Marina E.,Uvarov, Mikhail N.,Kazantsev, Maxim S.,Mostovich, Evgeny A.,Postulka, Lars,Eibisch, Paul,Wolf, Bernd,Lang, Michael,Postnikov, Pavel S.,Baumgarten, Martin
, p. 159 - 162 (2020)
An antiferromagnetically (AFM) coupled biradical based on oxoverdazyl and nitronylnitroxide was synthesized in 46 % yield using Sonogashira coupling. The obtained heterobiradical evidenced distinct properties of both radical entities in solution. Dependin
Cascade reactions of Me3Si-substituted imidazolidine-1,3-diols with PbO2, including oxidation of the corresponding diol and subsequent elimination of the trimethylsilyl fragment
Tretyakov, Eugene,Romanenko, Galina,Ikorskii, Vladimir,Stass, Dmitry,Vasiliev, Vladimir,Demina, Maria,Mareev, Alexander,Medvedeva, Alevtina,Gorelik, Elena,Ovcharenko, Victor
, p. 3639 - 3647 (2008/03/18)
It was found that reactions of 2-Me3Si-R-substituted (Si-C sp or Si-Csp2) imidazolidine-1,3-diols with PbO 2 in MeOH are cascade reactions, which involve the oxidation of imidazolidine-1,3-diols into nitronyl ni
Spin exchange interaction through phenylene-ethynylene bridge in diradicals based on iminonitroxide and nitronylnitroxide radical derivatives. 1. Experimental investigation of the through-bond spin exchange coupling
Wautelet, Pascale,Le Moigne, Jacques,Videva, Vladimira,Turek, Philippe
, p. 8025 - 8036 (2007/10/03)
A series of bis-iminonitroxide diradical derivatives of different lengths and geometry have been prepared that incorporate a conjugated phenylene-ethynylene bridge as a rigid spacer. This paper describes the synthesis of these new components and their main characterizations. An unexpected singlet ground state and substituent effects on the singlet-triplet gap have been found for substituted "m-phenylene"-based diradicals. The effects of the π-conjugation on the intramolecular through-bond spin coupling have been investigated by changing the length of the spacer within linear derivatives. The EPR studies demonstrate the intramolecular magnetic coupling between the radical spins within all compounds. This result is very attractive and unusual, given the large distance between the radicals from 15 A in the dimer to 36 A in the pentamer.
Cross-coupling of aryl iodides with paramagnetic terminal acetylenes derived from 4,4,5,5-tetramethyl-2-imidazoline-2-oxyl 3-oxide
Klyatskaya, S. V.,Tretyakov, E. V.,Vasilevsky, S. F.
, p. 128 - 134 (2007/10/03)
2-(Arylylethynylphenyl)-4,4,5,5-tetramethyl-2-imidazoline-1-oxyl 3-oxides 12 and 13 were synthesized by cross-coupling of aryl iodides with 1-alkynes containing the 4,4,5,5-tetramethyl-2-imidazoline-1-oxyl 3-oxide fragment. A procedure was developed for the preparation of 3-and 4-ethynyibenzaldehydes with the use of 2-methylbut-3-yn-2-ol.
