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1.
Инвентарный номер: нет.
   


   
    (A)symmetric chromophores based on cyano and fluorine-substituted 2,3-bis(5-arylthiophen-2-yl)quinoxalines: Synthesis, photophysical properties and application prospects / T. N. Moshkina, E. V. Nosova, A. E. Kopotilova [et al.] // Dyes and Pigments. - 2022. - Vol. 204. - Ст. 110434
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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2.
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    1,2,4,5-Tetrazine derivatives as components and precursors of photo- and electroactive materials / G. N. Lipunova, E. V. Nosova, G. V. Zyryanov [et al.] // Organic chemistry frontiers. - 2021. - Vol. 8, № 18. - P5182-5205
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Extensive research on the synthesis and application of tetrazine derivatives for electronic devices, luminescent elements, photoelectric conversion elements, and image sensors has been published recently. This review covers reported data on the modern trends in the design of functionalized tetrazines obtained within the period 2010–2020. Aryl(heteroaryl) and arylvinyl derivatives of tetrazines and their photoluminescence and application for fluorogenic probes are discussed. Examples of photosensitive oligomers and polymer 3,6-dithienyltetrazines are reviewed.

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3.
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    1,2,4-Triazino[5,6,1-i,j]quinolines: a new type of tricyclic analogs of fluoroquinolones [Electronic resource] / G. N. Lipunova, E. V. Nosova, N. N. Mochul`skaya, A. A. Andreiko, O. M. Chasovskikh, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2002. - Vol. 51, № 4. - P663-667
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of C-aryl-substituted amidrazones and S-methylisothiosemicarbazide with 3-ethoxy-2-polyfluorobenzoylacrylates results in corresponding N-(quinolin-1-yl)amidines that undergo conversion into derivatives of 1,2,4-triazino[5,6,1-i,j]quinoline by heating in acetic anhydride

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2002, 51 (4), 663.pdf
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4.
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    1,3,4-Oxa(thia)diazino [i,j]-annelated quinolines: a new type of key intermediate in the synthesis of tricyclic fluoroquinolones [Electronic resource] / G. N. Lipunova, E. V. Nosova, V. N. Charushin, L. P. Sidorova, O. M. Chasovskikh // Mendeleev Communications. - 1998. - Vol. 8, № 4. - P131-132
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The synthesis of new derivatives of 1,3,4-oxa(thia)diazino[6,5,4-i,j]quinolines, which have a structure that is very similar to the ofloxacin skeleton, by intramolecular cyclizations of ethyl 3-(R-carbonylhydrazino)- and 3-(R-thiocarbonylhydrazino)-substituted 2-polyfluorobenzoyl acrylates, is described??????

\\\\expert2\\nbo\\Mendeleev Communications\\1998, v.8, N 4. p.131.pdf
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5.
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    2-Hydroxybenzaldehyde (2-phenylquinazolin-4-yl)hydrazones [Electronic resource] / T. V. Trashakhova, E. V. Nosova, P. A. Slepukhin, M. S. Valova, G. N. Lipunova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2011. - Vol.60, №11. - С. 2347-2353. - Bibliogr. : p. 2353 (23 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SALICYLIDENEHYDRAZINE -- ZINC(II) COMPLEXES -- PHOTOLUMINESCENT
Аннотация: N-(2-Phenylquinazolin-4-yl)-N´ salicylidenehydrazines and their ZnII complexes were obtained. The structures and luminescent properties of these new quinazoline derivatives were examined

\\\\expert2\\NBO\\Russian Chemical Bulletin\\2011, 60 (11), 2347-2353.pdf
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6.
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    3-Phenyl/Pyridinyl Derivatives of Trans-2-(aryl/heteryl)vinyl-3H-quinazolin-4-ones: Synthesis and Fluorescent Properties / E. V. Nosova, T. V. Stupina, G. N. Lipunova, M. S. Valova, P. A. Slepukhin, V. N. Charushin // International Journal of Organic Chemistry. - 2012. - Vol.2, №1. - С. 56-63. - Bibliogr.: p. 61-63 (28 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
STYRYL BENZAZINES -- X-RAY -- FL SPECTRA

\\\\expert2\\NBO\\International Journal of Organic Chemistry\\2012. v. 2, N 1. P. 56-63.pdf
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7.
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    8,9,10-Trifluoro-6-oxo-6H-pyrido[1,2-a]quinoline-5-carbonitrile in the synthesis of novel 1-heteryl-3,3-dimethyl-3,4-dihydroisoquinolines [Electronic resource] / T. S. Vshivkova, Yu. V. Shklyaev, E. V. Nosova, G. N. Lipunova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2012. - Vol.61, №8. - С. 1650-1652
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
3,4-dihydroisoquinolines -- THREE-COMPONENT CONDENSATION -- ISOBUTYRALDEHYDE
Аннотация: 3,4-Dihydroisoquinolines containing the 8,9,10-trifluoro-6H-pyrido[1,2-a]quinolin-6-one substituent in position 1 were obtained by three-component reactions between arenes, isobutyraldehyde, and 8,9,10-trifluoro-6-oxo-6H-pyrido[1,2-a]quinoline-5-carbonitrile in H2SO4

\\\\expert2\\NBO\\Russian Chemical Bulletin\\2012, 61 (8), 1650-1652.pdf
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8.
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   A 10


   
    A new approach to fluorinated 4(1H)-quinazolinones [Electronic resource] / A. A. Layeva, E. V. Nosova, G. N. Lipunova, T. V. Trashakhova, V. N. Charushin // Journal of Fluorine Chemistry. - 2007. - Vol. 128, № 7. - P748-754
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A new approach for the synthesis of fluorinated 1H-quinazolin-4-ones and 4-substituted quinazolines has been developed. 6-Fluoro-1H-quinazolin-4-ones were obtained by intramolecular cyclization of fluorine-containing S-ethyl N-benzoylisothioureas. Nucleophilic substitution reactions at positions 2 and 7, as well as alkylation at 1-position of quinazolinones were investigated. In addition, the synthesis of fluorine-containing 4-aminoquinazolines was carried out.

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2007, v.128. p.748.pdf
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9.
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   A 99


   
    Azapyrene-based fluorophores: synthesis and photophysical properties / O. S. Taniya, A. F. Khasanov, M. V. Varaksin [et al.] // New Journal of Chemistry. - 2021. - Vol. 45, № 45. - P20955-20971
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Azapyrenes are the nitrogen isosteres of pyrene. Based on theoretical and experimental studies, electron–acceptor azapyrene domains may be considered as convenient scaffolds for constructing a large variety of “push–pull” π-conjugated chromophores with pronounced ICT properties. Over the past decade, due to the unrelenting interest in functional materials and modern methodologies such as cross-coupling, peri-annulation, direct C–H-functionalization, etc., methods for the synthesis of aryl(alkyl) K-functionalized azapyrenes and other derivatives have been developed, and their photophysical and electrochemical properties have been studied. This short review aims at critical analysis of the best known/modern methods for the preparation of functionalized azapyrene derivatives, as well as an assessment of their photophysical/electrochemical properties in comparison with the structural and electronic properties of the parent pyrene.

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10.
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   A 99


   
    Azinylarylethenes: synthesis and photophysical and photochemical properties [Electronic resource] / G. N. Lipunova, E. V. Nosova, T. V. Trashakhova, V. N. Charushin // Russian Chemical Reviews. - 2011. - Vol.80, №11. - С. 1115-1133. - Bibliogr. : p. 1131-1133 (124 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
AZINYLARYLETHENES -- SYNTHESIS -- STYRYLAZINES
Аннотация: Methods for the synthesis of styrylazines and styrylbenzazines are considered, their photophysical and photochemical properties are analyzed. The review covers both published data and own works of the authors. Important data on the prospects of application of arylhetarylethenes as components of electroluminescence materials are discussed

\\\\expert2\\NBO\\Russian Chemical Reviews\\2011, V.80, N11, p.1115.pdf
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