Главная Новые поступления Описание Шлюз Z39.50

Базы данных


Публикации Чарушина В.Н. - результаты поиска

Вид поиска
Каталог книг и продолжающихся изданий
Сводный каталог иностранных периодических изданий, имеющихся в библиотеках УрО РАН
Сводный каталог отечественных периодических изданий, имеющихся в библиотеках УрО РАН
Каталог диссертаций и авторефератов диссертаций УрО РАН
Каталог препринтов УрО РАН (1975 г. - )
Имидж-каталог отечественных книг (до 2010 г.)
Имидж-каталог иностранных книг (до 2010 г.)
Алфавитно-предметный указатель (АПУ) ЦНБ УрО РАН
Публикации об УрО РАН
Изобретения уральских ученых
Интеллектуальная собственность (статьи из периодики)
Нанотехнологии
Демидовские премии
Гибель династии Романовых
История Урала
Личная библиотека С. В. Вонсовского
Книжная коллекция Шубиных
Труды Института высокотемпературной электрохимии УрО РАН
Труды Института истории и археологии УрО РАН
Труды сотрудников Института горного дела УрО РАН
Труды сотрудников Института органического синтеза УрО РАН
Труды сотрудников Института теплофизики УрО РАН
Труды сотрудников Института химии твердого тела УрО РАН
Расплавы
Труды сотрудников ЦНБ УрО РАН
Публикации Черешнева В.А.
Публикации Чарушина В.Н.
Каталог библиотеки ИЭРиЖ УрО РАН
Электронная энциклопедия «Дискурсология»
Библиометрия
Область поиска
в найденном
 Найдено в других БД:Труды сотрудников Института органического синтеза УрО РАН (81)
Формат представления найденных документов:
полныйинформационныйкраткий
Отсортировать найденные документы по:
авторузаглавиюгоду изданиятипу документа
Поисковый запрос: (<.>A=Nosova, E. V.$<.>)
Общее количество найденных документов : 75
Показаны документы с 1 по 20
 1-20    21-40   41-60   61-75 
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

Найти похожие
2.
Инвентарный номер: нет.
   

   
    Synthesis and photophysical properties of pyridyl- and quinolinyl-substituted bis(arylthienyl)pyridines / T. N. Moshkina, E. V. Nosova, A. E. Kopotilova [et al.] // Journal of photochemistry and photobiology A: Chemistry. - 2022. - Vol. 427. - Ст. 113805
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие
3.
Инвентарный номер: нет.
   

   
    Synthesis and photophysical properties of pyridyl- and quinolinyl-substituted 4-(4-aminophenyl)quinazolines / T. N. Moshkina, E. V. Nosova, A. E. Kopotilova [et al.] // Journal of photochemistry and photobiology A: Chemistry. - 2022. - Vol. 429. - Ст. 113917
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие
4.
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.

Найти похожие
5.
Инвентарный номер: нет.
   
   T 44

   
    The Rh(III)-catalysed C-H/N-H annulation of 2-thienyl- and 2-phenyl-quinazolin-4(3: H)-ones with diphenylacetylene / T. N. Moshkina, E. V. Nosova, G. N. Lipunova [et al.] // New Journal of Chemistry. - 2021. - Vol. 45, № 19. - P8456-8466
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A series of 4,5-diphenyl-7H-thieno[2′,3′:3,4]pyrido[2,1-b]quinazolin-7-ones was synthesized via the Rh(III)-catalyzed annulation of 2-thienylquinazolin-4(3H)-ones with diphenylacetylene. 2-Phenylquinazolin-4(3H)-one amide alcoholysis and double C–H functionalization proceeded under the same reaction conditions with the formation of 2,3,7,8-tetraphenyl-1H-benzo[d,e][1,8]-naphthyridine derivatives. All compounds possess fluorescence properties in MeCN and toluene solutions as well as in the solid state. The aggregation induced emission (AIE) properties and the ability to detect Fe3+ cations were evaluated.

Найти похожие
6.
Инвентарный номер: нет.
   

    Mochulskaya, N. N.
    Antiviral agents – benzazine derivatives / N. N. Mochulskaya, E. V. Nosova, V. N. Charushin // Chemistry of heterocyclic compounds. - 2021. - Vol. 57. - С. 374–382
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BENZAZINES -- QUINAZOLINE -- QUINOLINE -- QUINOXALINE
Аннотация: The review outlines the results of studies of the antiviral activity of quinoline, quinoxaline, and quinazoline derivatives published over the past 5 years. The supplied data indicate the enormous potential of benzazines for the design of effective antiviral drugs.

Найти похожие
7.
Инвентарный номер: нет.
   

   
    Synthesis of “push-pull” fluorophores based on 2-aryl(heteryl)quinazolines / T. N. Moshkina, A. E. Kopotilova, E. V. Nosova [et al.] // Mendeleev 2021: book of abstracts XII international conference on chemistry for young scientists. - Saint Petersburg, 2021. - P607
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие
8.
Инвентарный номер: нет.
   

   
    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.

Найти похожие
9.
Инвентарный номер: нет.
   

   
    Substituted 2-(2-hydroxyphenyl)–3H-quinazolin-4-ones and their difluoroboron complexes: Synthesis and photophysical properties / T. N. Moshkina, E. V. Nosova, V. N. Charushin [et al.] // Spectrochimica acta part A: molecular and biomolecular spectroscopy. - 2021. - Vol. 252. - P119497
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ESIPT -- FLUORESCENCE -- O-LIGAND -- BF2-COMPLEX2-(2-HYDROXYPHENYL)–3H-QUINAZOLIN-4-ONES
Аннотация: 2-(2-Hydroxyphenyl)–3H-quinazolin-4-ones with diverse substituents at phenol ring and their six-membered difluoroboron complexes have been synthesized via few-stage approach. The photophysical properties of target compounds have been investigated in two solvents as well as in the solid state. The nature of substituents and substitution point in the phenol moiety of ligands and resulting BF2-complexes on the photophysical properties of dyes have been explored. The complex bearing two t-Bu groups proved to be the most emissive in solid state, whereas its 5-methoxy and 4-diethylamino counterparts possess strong emission in toluene solution. The dyes exhibited large Stokes shifts which was attributed to excited state intramolecular proton transfer (ESIPT). Additionally, fluorescence of quinazolinones in the mixture of THF/water was studied. All ligands demonstrated emission enhancement with increase of water fraction which was due to aggregation induced emission.

Найти похожие
10.
Инвентарный номер: нет.
   

   
    Synthesis and photophysical studies of novel v-shaped 2,3-bis{5-aryl-2-thienyl}(dibenzo[f,h])quinoxalines / T. N. Moshkina, E. V. Nosova, A. E. Kopotilova [et al.] // Asian journal of organic chemistry. - 2020. - Vol. 9, № 4. - P673-681
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CROSS-COUPLING -- DIBENZO[F,H]QUINOXALINE -- DONOR-ACCEPTOR-DONOR CHROMOPHORES -- FLUORESCENCE -- SENSORS
Аннотация: A series of novel V-shaped luminophores containing electron-withdrawing dibenzo[f,h]quinoxaline core and arylthienyl donor fragments at positions 2 and 3 has been synthesized. The absorption spectra (UV/vis) were recorded in several solvents, whereas emission spectra were recorded in solutions and powders. The solvatochromism as well as halochromism of obtained compounds was also explored. Electronic-structure calculations using quantum-chemistry methods were performed to further analyse experimental results. All characteristics were compared with that of 2,3-bis(arylthienyl)quinoxaline counterparts. The halochromic effect studies showed that upon gradual addition of trifluoroacetic acid (TFA) to the toluene solution of diethylaminophenyl-substituted dibenzo[f,h]quinoxaline chromophore, absorption and emission changed. Observed band shifts were more distinct in the case of mentioned quinoxaline than for other derivatives. All of the (dibenzo[f,h])quinoxaline chromophores exhibited good sensitivity toward nitro-containing explosives with high Stern-Volmer constants up to 57800 M−1, these results are remarkable for such heterocyclic systems.

Найти похожие
11.
Инвентарный номер: нет.
   

   
    Synthesis of novel 8-nitrosubstituted 1,3-benzothiazin-4-ones / E. V. Nosova, O. A. Batanova, G. N. Lipunova, V. N. Charushin // Mendeleev Communications. - 2020. - Т. 30, № 4. - P427
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие
12.
Инвентарный номер: нет.
   

   
    Synthesys and photophysical properties of 2-(het)arylderivatives of 4-morpholinylquinazolines / E. V. Nosova, T. N. Moshkina, Ju. V. Permyakova [et al.] // Actual problems of organic chemistry and biotechnology. - Екатеринбург, 2020. - P281-283
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
4-(4-MORPHOLINYL)QUINAZOLINES -- CROSS-COUPLING -- FLUORESCENCE

Найти похожие
13.
Инвентарный номер: нет.
   

    Moshkina, T. N.
    BF2 complexes based on 4-phenylquinazoline: synthesis and photophysical properties / T. N. Moshkina, E. V. Nosova, G. N. Lipunova, V. N. Charushin // Актуальные направления фундаментальных и прикладных исследований: Материалы XXII международной научно-практической конференции. - Morrisville, 2020. - P86-88
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие
14.
Инвентарный номер: нет.
   

   
    Synthesis and photophysical studies of novel 2-[5-(4-diethylaminophenyl)thiophen-2-yl]quinazoline derivatives / E. V. Nosova, T. N. Moshkina, D. S. Kopchuk, V. N. Charushin, G. N. Lipunova, I. V. Baklanova , P. A. Slepukhin // Mendeleev communications. - 2018. - Vol. 28, № 1. - С. 14-16
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие
15.
Инвентарный номер: нет.
   

   
    Synthesis and photophysical studies of novel 4-aryl substituted 2-phenyl-, 2-(fluoren-2-yl)- and 2-cymantrenylquinazolines / E. V. Nosova, T. N. Moshkina, V. N. Charushin, G. N. Lipunova, P. A. Slepukhin, I. V. Baklanova, E. S. Kelbysheva, N. M. Loim // Mendeleev Communications. - 2018. - Vol. 28, № 1. - P33-35
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие
16.
Инвентарный номер: нет.
   
   N 52

   
    New quinazoline derivatives as perspective components for optical materials / E. V. Nosova, T. N. Moshkina, G. N. Lipunova, V. N. Charushin // Успехи синтеза и комплексообразования = Advances in synthesis and complexing: Сборник тезисов четвертой Международной научной конференции. - Москва : РУДН, 2017. - Ч. 1 : Секция «Органическая химия». - P82
ББК 24
Рубрики: ХИМИЧЕСКИЕ НАУКИ

\\\\Expert2\\NBO\\статьи из сборников\\Успехи синтеза и комплексообразования 2017 Ч. 1 С. 82.pdf
Найти похожие
17.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis and Photophysical Studies of 2-(Thiophen-2-yl)-4-(morpholin-4-yl) quinazoline Derivatives [Electronic resource] / E. V. Nosova, T. N. Moshkina, G. N. Lipunova, D. S. Kopchuk, P. A. Slepukhin, I. V. Baklanova , V. N. Charushin // European Journal of Organic Chemistry. - 2016. - № 16. - С. 2876-2881
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PHOTOPHYSICS -- CHARGE TRANSFE -- FLUORESCENCE
Аннотация: The synthesis of a series of push-pull aryl and arylethynyl 2-(thiophen-2-yl) quinazoline derivatives is presented. The photophysical properties of the newly generated compounds are also described. Functionalization of the (2-thienyl) quinazoline fluorophore at the 5'-position with aryl and arylethynyl moieties was performed using bromination and subsequent palladium-catalyzed cross-coupling reactions. Optical studies revealed that 4-(diethylamino) phenyl and 4-(diphen-ylamino) phenyl derivatives emit green light upon irradiation, whereas their 4-(9H-carbazol-9-yl) phenyl, methoxyphenyl, thienyl and arylethynyl counterparts are characterized by blue light emission capabilities. The effect of protonation has also been studied, and the ability of some of these molecules to function as colorimetric and luminescent pH sensors has been demonstrated with significant color changes and luminescence switching upon the introduction of acid.

\\\\expert2\\NBO\\European Journal of Organic Chemistry\\2016, №16. p.2876-2881.pdf
Найти похожие
18.
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
Найти похожие
19.
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
Найти похожие
20.
Инвентарный номер: нет.
   
   F 70

   
    Fluorine-containing indazoles: Synthesis and biological activity / G. N. Lipunova, E. V. Nosova, V. N. Charushin, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2016. - Vol. 192. - С. 1-21. - Bibliogr. : p. 19-21 (108 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
INDAZOLES -- SYNTHESIS -- FLUORINE-CONTAINING INDAZOLES
Аннотация: New synthetic approaches to fluorinated indazoles, as well as the features of their biological properties are presented and discussed in the frames of this review article.

\\\\expert2\\nbo\\Journal of Fluorine Chemistry\\2016,V.192, p.1-21.pdf
Найти похожие
 1-20    21-40   41-60   61-75 
 
Описание базы данных
Стандартный
По словарю
Расширенный
ГРНТИ-навигатор
Статистика обращений

Сиглы отделов ЦНБ УрО РАН


  бр.ф. - Бронированный фонд

  бф - Научно-библиографический отдел

  БХЛ - Фонд художественной литературы

  ИИиА -Фонд исторической литературы в ЦНБ УрО РАН

  ИМЕТ -Отдел ЦНБ в Институте металлургии УрО РАН

  кх - Отдел фондов (книгохранениe)

  МБА - Межбиблиотечный абонемент

  мф - Методический фонд

  ок - Отдел научной каталогизации

  оку - Отдел комплектования и учета

  орф - Обменно-резервный фонд

  пф - Читальный зал деловой и патентной информации

  рк - Фонд редкой книги

  ч/з - Главный читальный зал

  эр - Зал электронных ресурсов

  

Сиглы библиотек институтов и НЦ УрО РАН
© Международная Ассоциация пользователей и разработчиков электронных библиотек и новых информационных технологий
(Ассоциация ЭБНИТ)
Яндекс.Метрика