1240404-70-9Relevant academic research and scientific papers
The molecular structure of N,N′-disulfinyl-3,4,5,6-tetrafluoro-1,2-diaminobenzene: A computational and X-ray diffraction study
Makarov, Arkady G.,Bagryanskaya, Irina Yu.,Gatilov, Yuri V.,Makarov, Alexander Yu.,Tersago, Karla,Alsenoy, Christian Van,Blockhuys, Frank,Zibarev, Andrey V.
, p. 158 - 162 (2010)
According to the results of quantum chemical calculations at various levels of theory, an isolated molecule of the title compound prefers a non-planar Z,Z configuration, which is very similar to the configuration observed in the crystal. This is in contra
Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
Mikhailovskaya, Tatiana F.,Makarov, Arkady G.,Selikhova, Natalia Yu.,Makarov, Alexander Yu.,Pritchina, Elena A.,Bagryanskaya, Irina Yu.,Vorontsova, Elena V.,Ivanov, Igor D.,Tikhova, Vera D.,Gritsan, Nina P.,Slizhov, Yuri G.,Zibarev, Andrey V.
, p. 44 - 58 (2016)
Previously unknown mono-, di- and in some cases tri- and tetra- carbocycle-substituted quinoxalines (2–8), 2,1,3-benzothiadiazoles (11, 12, 14–17) and 2,1,3-benzoselenadiazoles (20-25) were synthesized by nucleophilic substitution of fluorine in 5,6,7,8-t
The molecular structure of N,N'-disulfinyl-3,4,5,6-tetrafluoro-1,2- diaminobenzene: A computational and X-ray diffraction study
Makarov, Arkady G.,Bagryanskaya, Irina Yu.,Gatilov, Yuri V.,Makarov, Alexander Yu.,Tersago, Karla,Van Alsenoy, Christian,Blockhuys, Frank,Zibarev, Andrey V.
experimental part, p. 158 - 162 (2011/01/08)
According to the results of quantum chemical calculations at various levels of theory, an isolated molecule of the title compound prefers a non-planar Z,Z configuration, which is very similar to the configuration observed in the crystal. This is in contra
