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Публикации Черешнева В.А.
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1.
Инвентарный номер: нет.
   

   
    Sorption selectivity of palladium(II) by poly(N-2-sulfoethylallylamine) under static and dynamic conditions / L. M. Alifkhanova, Yu. S. Petrova, K. Ya. Kuznetsova [et al.] // Russian Journal of Applied Chemistry. - 2022. - Vol. 95, № 3. - P451-459
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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2.
Инвентарный номер: нет.
   

    Shishmakov, A. B.
    Few-step synthesis of PdO/TiO2 and Pd/TiO2 xerogels / A. B. Shishmakov, Yu. V. Mikushina, O. V. Koryakova // Inorganic Materials. - 2021. - Vol. 57, № 2. - P164-170
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
XEROGEL -- TITANIUM DIOXIDE -- PALLADIUM
Аннотация: We demonstrate a few-step technique for the synthesis of PdO/TiO2 and Pd/TiO2 (0.1–2.0 wt % Pd) xerogels, which comprises hydrolysis of a palladium nitrate solution in titanium tetrabutoxide in the vapor atmosphere over an aqueous acetic acid solution, drying, and calcination of the material between 800 and 870°C. According to X-ray diffraction and electron microscopy characterization results, after calcination at 800°C the xerogels contained palladium in the form of PdO particles ≤3–5 nm in size. The highly dispersed palladium(II) oxide covered the surface of the rutile crystallites and filled pores in between. Throughout the range of Pd(NO3)2 concentrations studied, the PdO particles were identical in size. In the material calcined at 870°C, palladium had the form of metallic particles ranging in diameter from 55 to 420 nm. Raising the palladium nitrate concentration in titanium tetrabutoxide was shown to increase the average size of the Pd particles.

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3.
Инвентарный номер: нет.
   
   F 33

   
    Features of sorption preconcentration of noble metal ions with sulfoethylated amino polymers / L. M. Alifkhanova, K. Y. Lopunova, A. A. Marchuk [и др.] // Russian journal of inorganic chemistry. - 2021. - Vol. 66, № 6. - С. 909-915
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Dependencies for the sorption of palladium(II), gold(III), and platinum(IV) chloro complexes from individual and binary solutions with sorbents based on sulfoethylated polyallylamine and poly(aminostyrene) have been obtained. It has been found that predominant sorption mechanism is complexation with functional groups of the sorbents for gold(III) and palladium(II) and ion exchange for platinum(IV). It has been shown that increase in the sulfoethylation degree of aminopolymer matrix leads to decrease of platinum(IV) sorption and therefore, to increase in palladium(II) sorption selectivity relative to this ion. This effect is the largest for the sorbents based on polyallylamine. The conditions of quantitative desorption of the studied metals from sorbent surface have been determined. The sorption of gold(III) by the sorbent based on polyallylamine has been shown to be complicated by gold(III) reduction in sorbent phase.

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4.
Инвентарный номер: нет.
   

   
    Effect of the degree of sulfoethylation of polyethylenimine on the selectivity of sorption of palladium(II) from binary solutions / E. I. Kapitanova, A. R. Sinelshchikova, Yu. S. Petrova [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 6. - P1161-1166
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYETHYLENIMINE -- SULFOETHYLATION -- SORPTION -- PLATINUM(IV) -- PALLADIUM(II) -- GOLD(III)

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5.
Инвентарный номер: нет.
   

   
    Oxidative C–H functionalization of arenes: main tool of 21st century green chemistry. A review / A. V. Shchepochkin, F. V. Antipin, V. N. Charushin, O. N. Chupakhin // Doklady Chemistry. - 2021. - Vol. 499, № 1. - P123-157
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Recent advances in the field of direct oxidative C–H functionalization of inactivated arenes, as one of the main tools of green chemistry, are discussed. Examples of building carbon–carbon, carbon–oxygen, carbon–nitrogen, and carbon–sulfur bonds, using catalysis with palladium compounds, oxidation with hypervalent iodine derivatives, and through electrochemical and photochemical transformations, are given.

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6.
Инвентарный номер: нет.
   

   
    Advances in transition-metal catalyzed carbonylative suzuki-miyaura coupling reaction: an update / D. Bhattacherjee, M. Rahman, S. Ghosh [et al.] // Advanced synthesis and catalysis. - 2021. - Vol. 363, № 6. - P1597-1624
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CARBONYLATION -- SUZUKI-MIYAURA COUPLING -- TRANSITION-METAL CATALYSIS
Аннотация: Transition metals have been an indispensable component of modern catalysis and among these palladium is the top-ranked choice of chemists as a catalyst. After the several important developments of palladium catalysed C−C cross-coupling reactions, carbonylative transformations have been realised as an attractive post modification of these reactions. Carbonylative Suzuki-Miyaura coupling reaction is among such transformations for direct incorporation of CO fragment for the preparation of biaryl or aryl/alkyl ketones via transition-metal catalysis. Ketone functionality is basically a valuable building block having huge pharmaceutical and agrochemical applications. Moreover, carbonylative Suzuki-Miyaura coupling is also used in the synthesis of various natural bioactive molecules through the direct joining of molecular fragments via CO bridge. In this review, the past decade developments in the carbonylative Suzuki-Miyaura coupling reactions are documented in detail with modern approaches in transition-metal catalysis.

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7.
Инвентарный номер: нет.
   

   
    Synthesis of heteroannulated indolopyrazines through domino N-H palladium-catalyzed/metal-free oxidative C-H bond activation / Y. A. Kvashnin, E. V. Verbitskiy, E. F. Zhilina [et al.] // ACS Omega. - 2020. - Vol. 5, № 25. - P15681-15690
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A convenient approach to [1,2,5]oxadiazolo[3′,4′:5,6]pyrazino[2,3-b]indoles and their heteroannulated analogues bearing various aryl substituents in the backbone has been developed. This synthetic protocol is based on Pd-catalyzed Buchwald–Hartwig and subsequent annulation by intramolecular oxidative cyclodehydrogenation. The photophysical properties for new polycycles have been measured.

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8.
Инвентарный номер: нет.
   
   I-60

   
    Influence of the degree of chitosan sulfoethylation on the sorption of palladium(ii) chloride complexes from multicomponent solutions / E. I. Kapitanova, A. A. Ibragimova, Y. S. Petrova, A. V. Pestov, L. K. Neudachina // Russian Journal of Applied Chemistry. - 2018. - Vol. 91, № 2. - P297-303
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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9.
Инвентарный номер: нет.
   
   A 10

   
    A new synthetic approach to fused nine-ring systems of the indolo[3,2-b] carbazole family through double Pd-catalyzed intramolecular C-H arylation [Electronic resource] / R. A. Irgashev, N. A. Kazin, G. A. Kim, G. L. Rusinov, V. N. Charushin // RSC Advances. - 2016. - Vol. 6, № 74. - С. 70106-70116
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
IGHT-EMITTING-DIODES -- BIPOLAR HOST MATERIALS -- HOLE-TRANSPORTING MATERIALS
Аннотация: A series of new polycyclic compounds bearing the 5,11-dihydroindolo[3,2-b] carbazole ring system, as the common motif of their nine-ring scaffolds, has been successfully prepared with the usage of an efficient two-step strategy, based on the double Friedel-Crafts acylation of 5,11-dihexyl-6,12-di(hetero) aryl-substituted 5,11-dihydroindolo[3,2-b] carbazoles with 2-iodobenzoyl chloride in the presence of SnCl4, followed by regioselective palladium-catalyzed cyclization of the obtained 2,8-bis(2-iodobenzoyl) derivatives into the desired fused 9H-fluoren-9-ones. Some modifications of these nine-ring structures have been performed to afford compounds of the same family bearing the 9H-fluorene fragments. Basic photophysical and electrochemical properties as well as thermal stability of the new fused indolo[3,2-b] carbazole derivatives have been determined.

\\\\expert2\\NBO\\RSC Advances\\2016. Vol. 6, N 74. P. 70106.pdf
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10.
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
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11.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of new bidentate ligands-terpene derivatives of ethylenediamine and their palladium complexes [Electronic resource] / O. A. Gur'eva, I. N. Alekseev, O. A. Zalevskaya, P. A. Slepukhin, A. V. Kutchin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2016. - Vol. 52, № 6. - С. 781-784
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PALLADIUM CHELATES -- DRUGS
Аннотация: New enantiomerically pure Schiff bases and palladium chelates based thereon were synthesized starting from (-)-alpha-pinene or (aEuro')-camphor and N,N-dimethylethane-1,2-diamine.

\\\\expert2\\NBO\\Russian Journal of Organic Chemistry\\2016, 52, (6), 781-784.pdf
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12.
Инвентарный номер: нет.
   
   A 10

   
    A new route towards dithienoquinazoline and benzo[f]thieno[3,2-h]quinazoline systems using Pd-catalyzed intramolecular cyclization under microwave irradiation [Electronic resource] / E. V. Verbitskiy, G. L. Rusinov, O. N. Chupakhin, V. N. Charushin // ARKIVOC. - 2016. - № 4. - С. 204-216
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PYRIMIDINES -- INTRAMOLECULAR CYCLIZATIONS -- FUSED RING SYSTEMS -- THIENOACENES
Аннотация: A novel synthetic route to novel thienoacene systems bearing a fused pyrimidine ring is proposed. The commercially available 5-bromopyrimidine is used as the starting material to obtain various dithienoquinazoline and benzo[f]thieno[3,2-h] quinazoline systems through the Suzuki cross-coupling, nucleophilic aromatic substitution of hydrogen (the S-N(H) reaction), and finally palladium-catalyzed intramolecular cyclization under microwave irradiation. Redox properties of some of the new compounds have been investigated. The data obtained show that these systems have plausible potential for use in organic electronic applications.

\\\\expert2\\NBO\\ARKIVOC\\2016, p.204-216.pdf
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13.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of 6-thienyl-substituted 2-amino-3-cyanopyridines [Electronic resource] / E. V. Verbitskiy, E. M. Cheprakova, M. G. Pervova, G. G. Danagulyan, G. L. Rusinov, O. N. Chupakhin, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2015. - С. 689-694. - Bibliogr. : p. 694 (25 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PYRIMIDINES -- TRANSFORMATIONS OF HETEROCYCLE -- PYRIDINES
Аннотация: An efficient method for the synthesis of 6-thienyl-substituted 2-amino-3-cyanopyridines by the ring transformation in the corresponding pyrimidines was developed. Further modification of the pyridines obtained under conditions of a room temperature aerobic Suzuki reaction in the presence of trans-bis(dicyclohexylamine) palladium(II) acetate as a catalyst was studied.

\\\\expert2\\nbo\\Russian Chemical Bulletin\\2015, 64 (3), 689-694.pdf
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14.
Инвентарный номер: нет.
   
   C 52

   
    Chiral palladium complexes with monoterpenoids oximes [Electronic resource] / O. A. Gur'eva, O. A. Zalevskaya, L. L. Frolova, I. N. Alekseev, P. A. Slepukhin, A. V. Kuchin // Russian Journal of General Chemistry. - 2014. - Vol.84, №1. - С. 137-142. - Bibliogr. : p. 142 (16 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CIS-VERBANONE -- MENTHONE -- OXIMES
Аннотация: Oximes of cis-caran-4-one, 3α- and 3β-hydroxycaran-4-ones, cis-verbanone, menthone, and 2β-hydroxybornan-3-one have been synthesized. The obtained oximes react with lithium tetrachloropalladate to give new chiral palladium complexes containing mono-or bidentate oxime ligands

\\\\expert2\\nbo\\Russian Journal of General Chemistry\\2014, V. 84, N 1, p. 137–142.pdf
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15.
Инвентарный номер: нет.
   
   T 98

   
    Two Approaches in the Synthesis of Planar Chiral Azinylferrocenes [Electronic resource] / I. A. Utepova, O. N. Chupakhin, P. O. Serebrennikova, A. A Musikhina, V. N. Charushin // Journal of Organic Chemistry. - 2014. - Vol. 79, № 18. - С. 8659-8667. - Bibliogr. : p. 8666-8667 (34 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHIRAL AZINYLFERROCENES -- CROSS-COUPLING REACTION -- HALOGENATED AZINES
Аннотация: Two synthetic routes to the chiral azinylferrocenes (CAFs) 5 and 15, key intermediates for the synthesis of new enantiomerically enriched P,N-ligands, have been compared. The first approach is based on the palladium-catalyzed cross-coupling reaction of halogenated azines with organozinc derivatives of ferrocenes (the Negishi reaction). The second approach exploits a new synthetic methodology, which provides a shorter pathway, through the direct C–H functionalization of aromatics by the C–C coupling of halogen-free (hetero)arenes with lithium ferrocenes bearing stereogenic C and S atoms. The palladium complexes of P,N-ligands have been used as catalysts for the Tsuji–Trost reaction, which proceeds with high enantioselectivity to give allylic substitution products in good yields.

\\\\expert2\\nbo\\Journal of Organic Chemistry\\2014, v.79, p.8659.pdf
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16.
Инвентарный номер: нет.
   
   D 62

   
    Direct C(sp2)-H Bond Functionalization in Cyclic Aldonitrones: Palladium(II)-Catalyzed Oxidative Cross-Coupling and Eliminative SNH Reactions / M. V. Varaksin, O. N. Chupakhin, V. N. Charushin, S. V. Mikhaylov, I. A. Utepova, B. A. Trofimov // 18th European Symposium on Organic Chemistry ESOC-2013, Marseille, France, 7-12 July 2013 : book of abstracts. - Marseille, France, 2013. - С. 329
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PALLADIUM(II) -- SNH REACTIONS -- CYCLIC ALDONITRONES

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17.
Инвентарный номер: нет.
   
   C 21

   
    Carboxyethenylation of polychlorobiphenyls / A. Mechaev, A. V. Pestov, Yu. G. Yatluk, M. G. Pervova, A. A. Panyukova // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2013. - Vol.49, №5. - С. 691-695. - Библиогр.: с. 695 (12 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BUTYL ACRYLATE -- PALLADIUM CATALYSTS -- POLYCHLOROBIPHENYLS
Аннотация: For the first time 2-carboxyethenylation was performed with butyl acrylate in the presence of palladium catalysts of bromine derivatives of polychlorobiphenyls obtained by bromination of polychlorobiphenyls. The haloderivatives of the butyl phenylcinnamate are readily hydrolyzed and hydrodehalogenized affording a mixture of phenylhydrocinnamic acids

\\\\expert2\\NBO\\Russian Journal of Organic Chemistry\\2013, 49, (5), 691-695.pdf
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18.
Инвентарный номер: нет.
   
   T 82

   
    Trans-Dichlorobis{(1R,4S)-1,7,7-trimethyl-3-[(S)-α-methylbenzylimino]bicyclo[2.2.1]heptan-2-one-N}Palladium(II): Synthesis and structural examination [Electronic resource] / O. A. Zalevskaya, O. A. Gur'eva, L. L. Frolova, I. N. Alekseev, P. A. Slepukhin, A. V. Kuchin // Russian Journal of Coordination Chemistry. - 2013. - Vol.39, №1. - P37-40
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PALLADIUM(II) -- SYNTHESIS -- STRUCTURAL EXAMINATION
Аннотация: A reaction of (1R,4S)-1,7,7-trimethyl-3-[(S)-α-methylbenzylimino]bicyclo[2.2.1]heptan-2-one with lithium tetrachloropalladate gave a chiral palladium(II) complex with monodentate coordination of the organic ligand. The structure of the complex was confirmed by NMR spectra and X-ray diffraction data

\\\\Expert2\\NBO\\Russian Journal of Coordination Chemistry\\2013, v. 39, N. 1, p.37.pdf
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19.
Инвентарный номер: нет.
   
   M 65

   
    Microwave-assisted palladium-catalyzed C–C coupling versus nucleophilic aromatic substitution of hydrogen (SNH) in 5-bromopyrimidine by action of bithiophene and its analogues [Электронный ресурс] / E. V. Verbitskiy, E. M. Cheprakova, E. F. Zhilina, M. I. Kodess, M. A. Ezhikova, M. G. Pervova, P. A. Slepukhin, V. N. Charushin // Tetrahedron. - 2013. - Vol.69, №25. - P5164-5172
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
C–H BOND ACTIVATIONS -- PYRIMIDINES -- PALLADIUM
Аннотация: 5-Bromopyrimidine reacts with 2,2′-bithiophene, [2,2′:5′,2″]terthiophene and 2-phenylthiophene in the presence of a palladium catalyst to give 5-(het)aryl substituted pyrimidines due to the palladium-catalyzed aryl–aryl C–C coupling. However 5-bromo-4-(het)aryl-pyrimidines have been prepared from the same starting materials through the SNH-reaction catalyzed by a Lewis acid. Conditions for both types of reactions were optimized. All components of the reaction mixtures, including by-products, have been elucidated by gas–liquid chromatography/mass-spectrometry. Evidence for the structure of 4- and 5-bithiophenyl-substituted pyrimidines has first been obtained by means of X-ray crystallography analysis. Molecular orbital calculations (TDDFT), as well as the redox and optical measurements for all new compounds have also been performed

\\\\Expert2\\NBO\\Tetrahedron\\2013, v. 68, p. 5164.pdf
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20.
Инвентарный номер: нет.
   
   P 17

   
    Palladium(II)-Catalyzed Oxidative C–H/C–H Coupling and Eliminative SNH Reactions in Direct Functionalization of Imidazole Oxides with Indoles / M. V. Varaksin, I. A. Utepova, O. N. Chupakhin, V. N. Charushin // Journal of Organic Chemistry. - 2012. - Vol.77, №20. - С. 9087-9093
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
IMIDAZOLE OXIDES -- INDOLES
Аннотация: Two novel synthetic approaches to realize the direct C(sp2)–H bond functionalization in cyclic nitrones are reported. Palladium(II)-catalyzed oxidative C–C coupling of 2,2-dialkyl-4-phenyl-2H-imidazole 1-oxides with indoles was shown to result in the formation of 5-indolyl-3-yl derivatives, while nucleophilic substitution of hydrogen (SNH) at C(5) of the same imidazole system was found to afford the corresponding deoxygenated compounds

\\\\Expert2\\nbo\\Journal of Organic Chemistry\\2010, v.77, p.9087.pdf
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  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

  

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