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Mendeleev Communications, 2001, том 11, выпуск 2, страницы 45–47
DOI: https://doi.org/10.1070/MC2001v011n02ABEH001372
(Mi mendc4209)
 

Эта публикация цитируется в 33 научных статьях (всего в 33 статьях)

Unsymmetrical porphyrazines with annulated 1,2,5-thia(seleno)diazole and 3,6-diamyloxybenzene rings: synthesis, characterization and X-ray crystal structure of H2{XN2}{3,6-(OAm)2Bz}3Pz (X = S, Se)

E. V. Kudrika, E. M. Bauerb, C. Ercolanib, A. Chiesi-Villab, C. Rizzolic, A. A. Gaberkorna, P. A. Stuzhina

a Department of Organic Chemistry, Ivanovo State University of Chemical Technology, Ivanovo, Russian Federation
b Dipartimento di Chimica, Universita degli Studi di Roma 'La Sapienza', Roma, Italy
c Dipartimento di Chimica Generale ed Inorganica, Universita di Parma, Italy
Аннотация: Cyclotetramerization of a mixture of 3,4-dicyano-1,2,5-thiadiazole or 3,4-dicyano-1,2,5-selenodiazole with 3,6-diamyloxyphthalodinitrile gives new unsymmetrical porphyrazines with annulated 1,2,5-thia(seleno)diazole and 3,6-diamyloxybenzene rings; the structures of the 1:3 products H2{XN2}{3,6-(OAm)2Bz}3Pz (X = S, Se) has been elucidated by single-crystal X-ray diffraction.
Тип публикации: Статья
Язык публикации: английский


Образец цитирования: E. V. Kudrik, E. M. Bauer, C. Ercolani, A. Chiesi-Villa, C. Rizzoli, A. A. Gaberkorn, P. A. Stuzhin, “Unsymmetrical porphyrazines with annulated 1,2,5-thia(seleno)diazole and 3,6-diamyloxybenzene rings: synthesis, characterization and X-ray crystal structure of H2{XN2}{3,6-(OAm)2Bz}3Pz (X = S, Se)”, Mendeleev Commun., 11:2 (2001), 45–47
Образцы ссылок на эту страницу:
  • https://www.mathnet.ru/rus/mendc4209
  • https://www.mathnet.ru/rus/mendc/v11/i2/p45
  • Эта публикация цитируется в следующих 33 статьяx:
    1. Jan Svec, Petr Zimcik, Lucie Novakova, Oleg A. Rakitin, Stanislav A. Amelichev, Pavel A. Stuzhin, Veronika Novakova, “1,2,5‐Chalcogenadiazole‐Annulated Tripyrazinoporphyrazines: Synthesis, Spectral Characteristics, and Influence of the Heavy Atom Effect on Their Photophysical Properties”, Eur J Org Chem, 2015:3 (2015), 596  crossref
    2. Ergün Gonca, “New soluble porphyrazine derivatives containing electron-rich substituents”, Journal of Coordination Chemistry, 66:10 (2013), 1720  crossref
    3. V. N. Knyukshto, D. I. Volkovich, L. L. Gladkov, V. A. Kuzmitsky, A. Ul-Haque, I. A. Popkova, P. A. Stuzhin, K. N. Solovyov, “Phenyl substituted Mg porphyrazines: The effect of annulation of a chalcogen-containing heterocycle on the spectral-luminescent properties”, Opt. Spectrosc., 113:4 (2012), 359  crossref
    4. Yasuhito Miyoshi, Kouji Takahashi, Takuya Fujimoto, Hirofumi Yoshikawa, Michio M. Matsushita, Yukio Ouchi, Mikael Kepenekian, Vincent Robert, Maria Pia Donzello, Claudio Ercolani, Kunio Awaga, “Crystal Structure, Spin Polarization, Solid-State Electrochemistry, and High n-Type Carrier Mobility of a Paramagnetic Semiconductor: Vanadyl Tetrakis(thiadiazole)porphyrazine”, Inorg. Chem., 51:1 (2012), 456  crossref
    5. Pavel A. Stuzhin, Maksim S. Mikhailov, Elena S. Yurina, Mikhail I. Bazanov, Oskar I. Koifman, Georgy L. Pakhomov, Vlad V. Travkin, Anna A. Sinelshchikova, “First tellurium-containing phthalocyanine analogues: strong effect of tellurium on spectral, redox and conductivity properties of porphyrazines with annulated chalcogenodiazole ring(s)”, Chem. Commun., 48:81 (2012), 10135  crossref
    6. Maria Pia Donzello, Elisa Viola, Mauro Giustini, Claudio Ercolani, Fabrizio Monacelli, “Tetrakis(thiadiazole)porphyrazines. 8. Singlet oxygen production, fluorescence response and liposomal incorporation of tetrakis(thiadiazole)porphyrazine macrocycles [TTDPzM] (M = MgII(H2O), ZnII, AlIIICl, GaIIICl, CdII, CuII, 2HI)”, Dalton Trans., 41:20 (2012), 6112  crossref
    7. Takuya Fujimoto, Yasuhito Miyoshi, Michio M. Matsushita, Kunio Awaga, “A complementary organic inverter of porphyrazine thin films: low-voltage operation using ionic liquid gate dielectrics”, Chem. Commun., 47:20 (2011), 5837  crossref
    8. Yasuhito Miyoshi, Takuya Fujimoto, Hirofumi Yoshikawa, Michio M. Matsushita, Kunio Awaga, Terufumi Yamada, Hiroshi Ito, “Photoconductivity and FET performance of an n-type porphyrazine semiconductor, tetrakis(thiadiazole)porphyrazine”, Organic Electronics, 12:2 (2011), 239  crossref
    9. Xue Cai, YueXing Zhang, DongDong Qi, JianZhuang Jiang, “Density functional theory study on organic semiconductor for field effect transistors: Symmetrical and unsymmetrical porphyrazine derivatives with annulated 1,2,5-thiadiazole and 1,4-diamyloxybenzene moieties”, Sci. China Ser. B-Chem., 52:6 (2009), 840  crossref
    10. Yoshiaki Shuku, Rie Suizu, Kunio Awaga, Osamu Sato, “Fe(II) spincrossover complex of [1,2,5]thiadiazolo[3,4-f][1,10]phenanthroline”, CrystEngComm, 11:10 (2009), 2065  crossref
    11. N. E. Galanin, G. P. Shaposhnikov, “Porphyrazines of symmetric and unsymmetrical structure with fused fragments of 1,4-bis(2-phenoxyethoxy)benzene and 5,6-diphenylpyrazine. Synthesis and spectral characteristics”, Russ J Org Chem, 45:5 (2009), 681  crossref
    12. Maria Pia Donzello, Claudio Ercolani, Xiaohui Cai, Karl M. Kadish, Giampaolo Ricciardi, Angela Rosa, “Tetrakis(thiadiazole)porphyrazines. 6. Spectroelectrochemical and Density Functional Theory Studies of the Anions [TTDPzM]n- (n = 1-4; M = ZnII, MgII(H2O), CuII, 2HI)”, Inorg. Chem., 48:20 (2009), 9890  crossref
    13. N. E. Galanin, E. V. Kudrik, G. P. Shaposhnikov, “Synthesis and spectral characteristics of phthalocyanines of unsymmetrical structure containing fragments of 3,6-didecyloxyphthalonitrile and 2-methyl-5,6-dicyanobenzimidazole”, Russ J Org Chem, 44:2 (2008), 225  crossref
    14. Matthew J. Fuchter, Chang Zhong, Hong Zong, Brian M. Hoffman, Anthony G. M. Barrett, “Porphyrazines: Designer Macrocycles by Peripheral Substituent Change”, Aust. J. Chem., 61:4 (2008), 235  crossref
    15. S. Yamazaki, Comprehensive Heterocyclic Chemistry III, 2008, 517  crossref
    16. P.A. Koutentis, Comprehensive Heterocyclic Chemistry III, 2008, 515  crossref
    17. Maria Pia Donzello, Claudio Ercolani, Luisa Mannina, Elisa Viola, Alëna Bubnova, Ol'ga G. Khelevina, Pavel A. Stuzhin, “Synthesis and Spectroscopic Properties of Low-Symmetry Tribenzoporphyrazines with Annulated 6H-1,4-Diazepine Ring”, Aust. J. Chem., 61:4 (2008), 262  crossref
    18. P. A. Stuzhin, I. V. Pimkov, A. Ul'-Khak, S. S. Ivanova, I. A. Popkova, D. I. Volkovich, V. A. Kuz'mitskii, M. -P. Donzello, “Synthesis and spectral properties of 1,2,5-thiadiazolo-, 1,2,5-selenadiazolo-, and benzo-fused β-phenyl-substituted porphyrazines”, Russ J Org Chem, 43:12 (2007), 1854  crossref
    19. Yasuhito Miyoshi, Megumi Kubo, Tasuku Fujinawa, Yosuke Suzuki, Hirofumi Yoshikawa, Kunio Awaga, “Electrochromism and Stable n‐Type Doping of Highly Oriented Thin Films of Tetrakis(thiadiazole)porphyrazine”, Angew Chem Int Ed, 46:29 (2007), 5532  crossref
    20. Yasuhito Miyoshi, Megumi Kubo, Tasuku Fujinawa, Yosuke Suzuki, Hirofumi Yoshikawa, Kunio Awaga, “Electrochromism and Stable n‐Type Doping of Highly Oriented Thin Films of Tetrakis(thiadiazole)porphyrazine”, Angewandte Chemie, 119:29 (2007), 5628  crossref
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