Аннотация:
At ambient temperature, interaction of the solid radical anion salt [Na(15-crown-5)][C2N4S2] with water vapour unexpectedly leads to the trithionate salt [Na(15-crown-5)]2[S(SO3)2], whose coordination pattern is very different from the previously studied trithionate salts.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
E. Lork, R. Mews, A. V. Zibarev, “Hydrolysis product of the [Na(15-crown-5)] salt of the [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl radical anion”, Mendeleev Commun., 19:3 (2009), 147–148
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3149
https://www.mathnet.ru/rus/mendc/v19/i3/p147
Эта публикация цитируется в следующих 16 статьяx:
Andrey V. Zibarev, Chalcogen Chemistry: Fundamentals and Applications, 2023, 168
Adam Le Gresley, Comprehensive Heterocyclic Chemistry IV, 2022, 120
Simon J. Coles, Sarah J. Fieldhouse, Wim T. Klooster, Anthony M.J. Lees, Andrew W.G. Platt, “Lanthanide tri- and tetrathionates and their complexes with triphenylphosphine oxide”, Polyhedron, 179 (2020), 114404
Nikolay A. Pushkarevsky, Elena A. Chulanova, Leonid A. Shundrin, Anton I. Smolentsev, Georgy E. Salnikov, Elena A. Pritchina, Alexander M. Genaev, Irina G. Irtegova, Irina Yu. Bagryanskaya, Sergey N. Konchenko, Nina P. Gritsan, Jens Beckmann, Andrey V. Zibarev, “Radical Anions, Radical‐Anion Salts, and Anionic Complexes of 2,1,3‐Benzochalcogenadiazoles”, Chemistry A European J, 25:3 (2019), 806
Oleg A. Rakitin, Andrey V. Zibarev, “Synthesis and Applications of 5‐Membered Chalcogen‐Nitrogen π‐Heterocycles with Three Heteroatoms”, Asian J Org Chem, 7:12 (2018), 2397
E. A. Chulanova, N. A. Semenov, N. A. Pushkarevsky, N. P. Gritsan, A. V. Zibarev, “Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles”, Mendeleev Commun., 28:5 (2018), 453–460
Maria R. Catalano, Anna L. Pellegrino, Patrizia Rossi, Paola Paoli, Paolo Cortelletti, Marco Pedroni, Adolfo Speghini, Graziella Malandrino, “Upconverting Er3+,Yb3+ activated β-NaYF4 thin films: a solution route using a novel sodium β-diketonate polyether adduct”, New J. Chem., 41:12 (2017), 4771
Lidia S. Konstantinova, Ekaterina A. Knyazeva, Oleg A. Rakitin, “Recent Developments in the Synthesis and Applications of 1,2,5-Thia- and Selenadiazoles. A Review”, Organic Preparations and Procedures International, 46:6 (2014), 475
Alexander Yu. Makarov, Elena A. Chulanova, Nikolay A. Semenov, Nikolay A. Pushkarevsky, Anton V. Lonchakov, Artem S. Bogomyakov, Irina G. Irtegova, Nadezhda V. Vasilieva, Enno Lork, Nina P. Gritsan, Sergey N. Konchenko, Victor I. Ovcharenko, Andrey V. Zibarev, “A novel sulfur–nitrogen π-heterocyclic radical anion, (6H-1,2,3-benzodithiazol-6-ylidene)malononitrilidyl, and its homo- and heterospin salts”, Polyhedron, 72 (2014), 43
R.T. Boeré, T.L. Roemmele, Comprehensive Inorganic Chemistry II, 2013, 375
Anton Lonchakov, Oleg Rakitin, Nina Gritsan, Andrey Zibarev, “Breathing Some New Life into an Old Topic: Chalcogen-Nitrogen π-Heterocycles as Electron Acceptors”, Molecules, 18:8 (2013), 9850
René T. Boeré, Electron Paramagnetic Resonance, 2012, 22
N. P. Gritsan, A. V. Zibarev, “Chalcogen-nitrogen π-heterocyclic radical anion salts: the synthesis and properties”, Russ Chem Bull, 60:11 (2011), 2131
Elizaveta A. Suturina, Nikolay A. Semenov, Anton V. Lonchakov, Irina Yu. Bagryanskaya, Yuri V. Gatilov, Irina G. Irtegova, Nadezhda V. Vasilieva, Enno Lork, Rüdiger Mews, Nina P. Gritsan, Andrey V. Zibarev, “Interaction of 1,2,5-Chalcogenadiazole Derivatives with Thiophenolate: Hypercoordination with Formation of Interchalcogen Bond versus Reduction to Radical Anion”, J. Phys. Chem. A, 115:18 (2011), 4851
Andrey V. Zibarev, Rüdiger Mews, Selenium and Tellurium Chemistry, 2011, 123
Nikolay A. Semenov, Nikolay A. Pushkarevsky, Anton V. Lonchakov, Artem S. Bogomyakov, Elena A. Pritchina, Elizaveta A. Suturina, Nina P. Gritsan, Sergey N. Konchenko, Ruediger Mews, Victor I. Ovcharenko, Andrey V. Zibarev, “Heterospin π-Heterocyclic Radical-Anion Salt: Synthesis, Structure, and Magnetic Properties of Decamethylchromocenium [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl”, Inorg. Chem., 49:16 (2010), 7558
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