Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1984, 49, 684-703
https://doi.org/10.1135/cccc19840684

1,2,3-Dithiazolyle, eine neue Klasse persistenter Radikale

Roland Mayera, Gunter Domschkea, Siegfried Bleischa, Jürgen Fabiana, Anton Bartlb and Andrej Staško

a Sektion Chemie der Technischen Universitaet Dresden, DDR
b Zentralinstut fur Festkoerperphysik und Werkstofforschung, Akademie der Wissenschaften der DDR, 8027 Dresden, DDR

Crossref Cited-by Linking

  • Buravlev Alexander A., Makarov Alexander Yu., Rakitin Oleg A., Zibarev Andrey V.: Wolmershäuser radicals: Chemistry and materials science. Mendeleev Communications 2023, 33, 439. <https://doi.org/10.1016/j.mencom.2023.06.001>
  • Makarov Alexander Yu., Volkova Yulia M., Zikirin Samat B., Irtegova Irina G., Bagryanskaya Irina Yu., Gatilov Yuri V., Nefedov Andrey A., Zibarev Andrey V.: New 3,1,2,4-benzothiaselenadiazines, related π-heterocycles including Herz cations, radicals and molecular complexes, and Bunte salts. New J. Chem. 2022, 46, 3687. <https://doi.org/10.1039/D1NJ05979C>
  • Nicholls Alexander J., Baxendale Ian R.: Benzo[1,2,3]dithiazole Compounds: A History of Synthesis and Their Renewed Applicability in Materials and Synthetic Chemistry, Originating from the Herz Reaction. Reactions 2021, 2, 175. <https://doi.org/10.3390/reactions2030013>
  • Volkova Yulia M., Makarov Alexander Yu., Pritchina Elena A., Gritsan Nina P., Zibarev Andrey V.: Herz radicals: chemistry and materials science. Mendeleev Communications 2020, 30, 385. <https://doi.org/10.1016/j.mencom.2020.07.001>
  • Rakitin Oleg A., Zibarev Andrey V.: Synthesis and Applications of 5‐Membered Chalcogen‐Nitrogen π‐Heterocycles with Three Heteroatoms. Asian J Org Chem 2018, 7, 2397. <https://doi.org/10.1002/ajoc.201800536>
  • Makarov Alexander Yu., Bagryanskaya Irina Yu., Volkova Yulia M., Shakirov Makhmut M., Zibarev Andrey V.: Salts of Sterically Hindered Chalcogen‐Varied Herz Cations Including Those with [Te3Cl14]2– and [Te4Cl18]2– Anions. Eur J Inorg Chem 2018, 2018, 1322. <https://doi.org/10.1002/ejic.201701470>
  • Konstantinova Lidia S., Baranovsky Ilia V., Pritchina Elena A., Mikhailov Maksim S., Bagryanskaya Irina Yu., Semenov Nikolay A., Irtegova Irina G., Salnikov Georgy E., Lyssenko Konstantin A., Gritsan Nina P., Zibarev Andrey V., Rakitin Oleg A.: Fused 1,2,3‐Thiaselenazoles Synthesized from 1,2,3‐Dithiazoles through Selective Chalcogen Exchange. Chemistry A European J 2017, 23, 17037. <https://doi.org/10.1002/chem.201703182>
  • Volkova Yulia M., Makarov Alexander Yu., Zikirin Samat B., Genaev Alexander M., Bagryanskaya Irina Yu., Zibarev Andrey V.: 3,1,2,4-Benzothiaselenadiazine and related heterocycles: synthesis and transformation into Herz-type radicals. Mendeleev Communications 2017, 27, 19. <https://doi.org/10.1016/j.mencom.2017.01.005>
  • Grayfer Tatiana D., Makarov Alexander Yu., Bagryanskaya Irina Yu., Irtegova Irina G., Gatilov Yuri V., Zibarev Andrey V.: Interaction of 1,3,2,4‐Benzodithiadiazines with Aromatic Phosphines and Phosphites. Heteroatom Chemistry 2015, 26, 42. <https://doi.org/10.1002/hc.21209>
  • Makarov Alexander Yu., Chulanova Elena A., Semenov Nikolay A., Pushkarevsky Nikolay A., Lonchakov Anton V., Bogomyakov Artem S., Irtegova Irina G., Vasilieva Nadezhda V., Lork Enno, Gritsan Nina P., Konchenko Sergey N., Ovcharenko Victor I., Zibarev Andrey V.: A novel sulfur–nitrogen π-heterocyclic radical anion, (6H-1,2,3-benzodithiazol-6-ylidene)malononitrilidyl, and its homo- and heterospin salts. Polyhedron 2014, 72, 43. <https://doi.org/10.1016/j.poly.2014.01.027>
  • Constantinides Christos P., Ioannou Theodosia A., Koutentis Panayiotis A.: Manipulating the singlet–triplet energy gaps of arene-fused bis(1,2,3-dithiazoles): A computational study. Polyhedron 2013, 64, 172. <https://doi.org/10.1016/j.poly.2013.03.054>
  • Makarov Alexander Yu., Blockhuys Frank, Bagryanskaya Irina Yu., Gatilov Yuri V., Shakirov Makhmut M., Zibarev Andrey V.: Experimental and Computational Study on the Structure and Properties of Herz Cations and Radicals: 1,2,3-Benzodithiazolium, 1,2,3-Benzodithiazolyl, and Their Se Congeners. Inorg. Chem. 2013, 52, 3699. <https://doi.org/10.1021/ic302203t>
  • Gritsan Nina P., Makarov Alexander Yu., Zibarev Andrey V.: A New Approach to Chalcogen–Nitrogen π-Heterocyclic Radicals. Appl Magn Reson 2011, 41, 449. <https://doi.org/10.1007/s00723-011-0240-6>
  • Pivtsov Andrey V., Kulik Leonid V., Makarov Alexander Yu., Blockhuys Frank: Pulse EPR and ENDOR study of 1,2,3-benzodithiazolyl, 2,1,3-benzothiaselenazolyl and 1,2,3-benzodiselenazolyl radicals. Phys Chem Chem Phys 2011, 13, 3873. <https://doi.org/10.1039/c0cp02051f>
  • Risto Maarit, Assoud Abdeljalil, Winter Stephen M., Oilunkaniemi Raija, Laitinen Risto S., Oakley Richard T.: Heavy Atom Analogues of 1,2,3-Dithiazolylium Salts: Preparation, Structures and Redox Chemistry. Inorg. Chem. 2008, 47, 10100. <https://doi.org/10.1021/ic8013738>
  • Gritsan Nina P., Kim Stanislav N., Makarov Alexander Yu., Chesnokov Eugenii N., Zibarev Andrey V.: Photochemistry of 1,3,2,4-benzodithiadiazines: formation and oxidation of 1,2,3-benzodithiazolyl radicals. Photochem Photobiol Sci 2006, 5, 95. <https://doi.org/10.1039/b510188c>
  • Oakley Richard T., Reed Robert W., Robertson Craig M., Richardson John F.: Naphthalene-1,2,3-Dithiazolyl and Its Selenium-Containing Variants. Inorg. Chem. 2005, 44, 1837. <https://doi.org/10.1021/ic048534e>
  • Beer Leanne, Brusso Jaclyn L., Cordes A. Wallace, Haddon Robert C., Itkis Mikhail E., Kirschbaum Kristin, MacGregor Douglas S., Oakley Richard T., Pinkerton A. Alan, Reed Robert W.: Resonance-Stabilized 1,2,3-Dithiazolo-1,2,3-dithiazolyls as Neutral π-Radical Conductors. J. Am. Chem. Soc. 2002, 124, 9498. <https://doi.org/10.1021/ja026118s>
  • Kaszynski Piotr: Theoretical Analysis of Heteroaromatic Thioaminyl Radicals. Part 1:  A Comparison of Ab Initio and Density Functional Methods in Calculations of Molecular Geometry and Isotropic Hyperfine Coupling Constants. J. Phys. Chem. A 2001, 105, 7615. <https://doi.org/10.1021/jp003459o>
  • Boeré René T, Roemmele Tracey L: Electrochemistry of redox-active Group 15/16 heterocyles. Coord Chem Rev - 2000, 210, 369. <https://doi.org/10.1016/S0010-8545(00)00349-0>
  • Barclay T. M., Cordes A. W., Haddon R. C., Itkis M. E., Oakley R. T., Reed R. W., Zhang H.: Preparation and Characterization of a Neutral π-Radical Molecular Conductor. J. Am. Chem. Soc. 1999, 121, 969. <https://doi.org/10.1021/ja983490s>
  • Barclay T. M., Beer L., Cordes A. W., Haddon R. C., Itkis M. I., Oakley R. T., Preuss K. E., Reed R. W.: trans-4,4‘-Dichloro-1,1‘,2,2‘,3,3‘-tetrathiadiazafulvalene (DC-TAF) and Its 1:1 Radical Cation Salts [DC-TAF][X]:  Preparation and Solid-State Properties of BF4-, ClO4-, and FSO3- Derivatives. J. Am. Chem. Soc. 1999, 121, 6657. <https://doi.org/10.1021/ja990933z>
  • Kim Kyongtae: Synthesis and Reactions of 1,2,3-Dithiazoles. Sulfur reports 1998, 21, 147. <https://doi.org/10.1080/01961779808047935>
  • Barclay T. M., Cordes A. W., Goddard J. D., Mawhinney R. C., Oakley R. T., Preuss K. E., Reed R. W.: Benzo-Bridged Bis(1,2,3-dithiazoles) and Their Selenium Analogues. Preparation, Molecular and Electronic Structures, and Redox Chemistry. J. Am. Chem. Soc. 1997, 119, 12136. <https://doi.org/10.1021/ja972927d>
  • Mayer Roland: ‘Schwefel-Mayer’ und Seine Schule: Vier Jahrzehnte Naturstoffchemie und Organische Schwefelchemie in Leipzig, Tharandt und Dresden. Sulfur Reports 1997, 20, 31. <https://doi.org/10.1080/01961779708047913>
  • Domschke G�nter, Walther Christiane, Tsch�pe Petra, Bartl Anton: C-Substituierte 1,2,3,5-Dithiadiazoliumsalze und 1,2,3,5-Dithiadiazolyle. J. Prakt. Chem. 1994, 336, 266. <https://doi.org/10.1002/prac.19943360315>
  • Oakley Richard T., Richardson John F., Spence Rupert E. V. H.: Tetrathiadiazafulvalenes; preparation and characterisation of cis- and trans-[RCNS2CCS2NCR](R = Me, Ph). J. Chem. Soc., Chem. Commun. 1993, 1226. <https://doi.org/10.1039/C39930001226>
  • Preston K. F., Sutcliffe L. H.: Electron spin resonance spectroscopy of free radicals containing sulphur linked to nitrogen. Magnetic Reson in Chemistry 1990, 28, 189. <https://doi.org/10.1002/mrc.1260280302>
  • Domschke Günter, Heimbold Ilka: Benzo[c] [1,2,5]thiadiazolo aus primären aromatischen Aminen und 1,3,5‐Trichlor‐1,3,5,2,4,6‐trithiatriazin. Zeitschrift fuer Chemie 1987, 27, 31. <https://doi.org/10.1002/zfch.19870270113>
  • Mayer Roland: S,N-Compounds via Amines and Sulphur Halides. Phosphorus and Sulfur and the Related Elements 1985, 23, 277. <https://doi.org/10.1080/03086648508073390>
  • MAYER R., DOMSCHKE G., BLEISCH S., FABIAN J., BARTL A., STASKO A.: ChemInform Abstract: 1,2,3‐DITHIAZOLYLS, A NEW CLASS OF PERSISTENT RADICALS. Chemischer Informationsdienst 1984, 15. <https://doi.org/10.1002/chin.198427107>