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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.
Инвентарный номер: нет.
   


   
    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.
Инвентарный номер: нет.
   
   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.
Инвентарный номер: нет.
   
   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.
Инвентарный номер: нет.
   
   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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11.
Инвентарный номер: нет.
   
   B 78


   
    Boron(III) Complexes with N,​N'- and N,​O-​Heterocyclic Ligands: Synthesis and Spectroscopic Properties [Electronic resource] / G. N. Lipunova, E. V. Nosova, V. N. Charushin, O. N. Chupakhin // Comments on Inorganic Chemistry. - 2016. - Vol. 2016. - С. 1153470
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PROPERTIES -- PREPARATION -- SYNTHETIC PREPARATION
Аннотация: This review is focused on consideration of effects of the nature of N,​N'- and N,​O-​bidentate ligands on the structure and optical properties of their B(III) complexes. It has been established that B(III) complexes with asym. N,​N'- and N,​O-​bidentate ligands, such as ortho-​hydroxyphenyl substituted azaheterocycles and heteryl-​β-​ketoimines, exhibit large Stokes shifts, enhanced intensity, and extended range for luminescence in solns. as well as in solid state, comparable with characteristics of the family of BODIPYs derivs. Complexes of some bidentate ligands can be considered as promising fluorophores for applications in biomedical imaging, electroluminescent, solar cell devices, and other fields.

\\\\expert2\\nbo\\Comments on Inorganic Chemistry\\2016. P. 1153470.pdf
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12.
Инвентарный номер: нет.
   
   C 47


    Charushin, V. N.
    Fluorinated derivatives of azaheterocycles [] / V. N. Charushin, E. V. Nosova, G. N. Lipunova // 20-th International Congress of Heterocyclic Chemistry, Palermo, July 31-August 5, 2005 : book of abstracts . - Palermo, Italy, 2005. - С. 506
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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13.
Инвентарный номер: нет.
   
   C 47


    Charushin, V. N.
    Fluorinated derivatives of condensed heterocycles on the basis of (polyfluorobenzoyl)chlorides [Text] : доклад, тезисы доклада / V. N. Charushin, E. V. Nosova, G. N. Lipunova // XXth European Colloquium on Heterocyclic Chemistry, Stockholm,Sweden, 18-21 Aug. 2002 г. - Stockholm, 2002. - PB:4
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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14.
Инвентарный номер: нет.
   
   C 47


    Charushin, V. N.
    Fluoroquinolones: Synthesis and Application / V. N. Charushin, E. V. Nosova, G. N. Lipunova // Fluorine in Heterocyclic Chemistry : Издательство "Springer", 2014. - Vol. 2. - С. 111-179. - Bibliogr. : p. 176-179 (377 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
QUINOLONE SYSTEM -- BIOLOGICAL ACTIVITY -- FLUOROQUINOLONES
Аннотация: The data on 6-fluorо-1,4-dihydroquinolin-4-oxo-3-carboxylic acids and their structural analogues accumulated in the literature for the last 10–15 years are reviewed. Synthetic approaches to the quinolone system, as well as all kind of structural modifications by incorporating substituents into 1–8 positions or by means of annelation have been discussed. The “structure-activity” relationships for antibacterial fluoroquinolones, as well as the data on other types of biological activity for the family of bi- and polycyclic fluoroquinolones are presented. The formation of complexes of fluoroquinolones with metals and their applications have been considered. The bibliography

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15.
Инвентарный номер: нет.
   
   C 98


   
    Cyclometallated Pt-II complexes of 2-(2-thienyl)-4-(cycloalkylimino)-substituted quinazolines [Electronic resource] / E. V. Nosova, T. N. Moshkina, D. S. Kopchuk, G. N. Lipunova, P. A. Slepukhin, V. N. Charushin // Mendeleev Communications. - 2016. - Vol. 26, № 2. - С. 129-130
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PLATINUM COMPLEXES -- DIODES
Аннотация: The title complexes were prepared based on 2-(thiophen-2-yl)-4-(morpholin-4-yl)- and 2-(thiophen-2-yl)-4-(piperidin-1-yl)-substituted quinazolines and found to exhibit luminescent properties

\\\\expert2\\NBO\\Mendeleev Communications\\2016, v.26, p. 129-130.pdf
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16.
Инвентарный номер: нет.
   
   F 70


   
    Fluorinated azines and benzazines containing oxygen or sulfur atoms [Text] / E. V. Nosova, G. N. Lipunova, V. N. Charushin, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2010. - Vol. 131, № 12. - P1267-1288
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: In the frames of this review article the recently obtained data on synthetic approaches to fluorinated oxa(thia)azines and benzazines, their chemical properties, structure, and biological activity have been analyzed

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2010, v. 131, p.1267.pdf
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17.
Инвентарный номер: нет.
   
   F 70


   
    Fluorinated benzazoles and benzazines [Text] / E. V. Nosova, N. N. Mochul`skaya, S. K. Kotovskaya, G. N. Lipunova, V. N. Charushin // Heteroatom Chemistry. - 2006. - Vol. 17, № 6. - P579-594. - Библиогр. : с. 592 (103 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The review surveys the recently obtained data on the synthesis of fluorinated benzazoles and benzazines.

\\\\expert2\\nbo\\Heteroatom Chemistry\\2006, V. 17, N 6, P. 579-564.pdf
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18.
Инвентарный номер: нет.
   
   F 70


   
    Fluorinated benzimidazo[1,2-a]quinolones [Electronic resource] / G. N. Lipunova, E. V. Nosova, E. B. Vasil'eva, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2003. - Vol. 52, № 2. - P457-460
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reactions of 2-cyanomethylbenzimidazole with polyfluorobenzoyl chlorides afforded 2-(1,3-dihydrobenzimidazol-2-ylidene)-3-oxo-3-polyfluorophenylpropionitriles. Refluxing of the latter compounds in acetonitrile in the presence of DBU or in dimethylformamide in the presence of amines gave rise to fluorine-containing derivatives of benzimidazo[1,2-a]quinolone

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2003, 52 (2), 457.pdf
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19.
Инвентарный номер: нет.
   
   F 70


   
    Fluorine containing quinoline and quinoxaline styryl derivatives: [Electronic resource] / E. V. Nosova, T. V. Trashakhova, V. S. Ustyugov, N. N. Mochul`skaya, M. S. Valova, G. N. Lipunova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2011. - Vol.60, №5. - С. 942-947. - Bibliogr. : p. 946-947 (25 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
STYRYLBENZAZINES -- PHOTOLUMINESCENCE -- 6,7-DIFLUOROQUINALDINE
Аннотация: (E)-2-Styryl-substituted 6,7-difluoroquinolines and quinoxalines were synthesized by the condensation of the corresponding 2 methylbenzazines with aromatic aldehydes. Photolumines cence of the synthesized 6,7 difluoro 2 styrylbenzazines was studied

\\\\expert2\\NBO\\Russian Chemical Bulletin\\2011, 60 (5), 942-947.pdf
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20.
Инвентарный номер: нет.
   
   F 70


   
    Fluorine-Containing Heterocycles. VIII. Transformations of 2-Polyfluorobenzoylacrylates Having a Thiosemicarbazide Fragment [Electronic resource] / G. N. Lipunova, E. V. Nosova, L. P. Sidorova, V. N. Charushin, O. M. Chasovskikh, A. V. Tkachev // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2002. - Vol. 38, № 12. - P1790-1796
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Depending on the conditions, 3-(4-R-thiosemicarbazido)-2-polyfluorobenzoylacrylates can be converted into the corresponding potassium salts, [1,3,4]thiadiazino[6,5,4-ij]quinolines, and pyrazole or 1,3,4-thiadiazole derivatives

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2002, 38 (12), 1790.pdf
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