A. F. Popov

ORCID: 0000-0002-5867-0598
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Research Areas
  • Chemical Reaction Mechanisms
  • Inorganic and Organometallic Chemistry
  • Analytical Chemistry and Chromatography
  • Surfactants and Colloidal Systems
  • Organic Chemistry Cycloaddition Reactions
  • Crystallization and Solubility Studies
  • Photochemistry and Electron Transfer Studies
  • Chemical Reactions and Mechanisms
  • Pesticide and Herbicide Environmental Studies
  • X-ray Diffraction in Crystallography
  • Chemical Synthesis and Analysis
  • Synthesis and Characterization of Heterocyclic Compounds
  • Pesticide Exposure and Toxicity
  • Environmental Chemistry and Analysis
  • Chemical Synthesis and Reactions
  • Organic and Inorganic Chemical Reactions
  • Organophosphorus compounds synthesis
  • Organic and Molecular Conductors Research
  • Crystallography and molecular interactions
  • Asymmetric Synthesis and Catalysis
  • Molecular Sensors and Ion Detection
  • Molecular spectroscopy and chirality
  • Chemical Thermodynamics and Molecular Structure
  • Coal and Coke Industries Research
  • Synthesis and Reactivity of Sulfur-Containing Compounds

National Academy of Sciences of Ukraine
2007-2019

Institute of Organic Chemistry
2019

Kharkiv National Automobile and Highway University
2019

Institute of Physical and Organic Chemistry
1984-2013

Donetsk State University of Internal Affairs
2011

University of California, Santa Barbara
2004

Durham University
1999

Donetsk National Technical University
1999

Russian Academy of Sciences
1996-1998

Donetsk Institute for Physics and Engineering named after O.O. Galkin
1993

Статтю присвячено пам’яті видатного українського вченого в галузі фізичної хімії, кінетики та каталізу, талановитого організатора науки, лауреата Державної премії України науки і техніки (1993, посмертно), імені Л.В. Писаржевського НАН (1969), директора Інституту геології геохімії горючих копалин (1982—1986), керівника Відділення фізико-хімії технології хімії ім. (1986—1991), доктора хімічних наук (1964), професора (1966), дійсного члена НТШ (1992, академіка (1973) Романа Володимировича...

10.15407/visn2025.03.090 article UK Visnik Nacional noi academii nauk Ukrai ni 2025-03-18

We report on a new approach for creating water-soluble functionalized vesicles employing N-alkyl-3-boronopyridinium triflates (alkyl = Me, C12H25, C16H33) as sensors monosaccharides. The nanoaggregate properties were studied by means of DLS, TEM, high-resolution (1)H NMR, and the solvatochromic dyes Reichardt's betaine Methyl Orange. shown to have 30-200 nm diameters depending amphiphile chain length. Diol binding was steady-state fluorescence UV-vis using Alizarin Red S probe in solution at...

10.1021/la304751p article EN Langmuir 2013-02-18

2,4,5,7-Tetranitro-9-fluorenone (1b) reacts readily with n-butanethiol in dipolar aprotic solvents selective substitution of nitro groups by butylsulfanyl positions 2 and 7 (2, 3); the 2,5-isomer 4 was formed only as a minor product (<1%). Condensation fluorenones 2-4 malononitrile yielded 9-dicyanomethylene derivatives 5-7, which showed strong intramolecular charge transfer (lambda approximately 510-560 nm) were found to sensitize photoconductivity carbazole-containing polymer films....

10.1021/jo991796r article EN The Journal of Organic Chemistry 2000-04-26

The synthesis and physical properties of four series novel fluorene push−pull compounds (4−7) the D−π−A type with intramolecular charge transfer (from 1,3- 1,2-dithiole 1,3-selenathiole donor (D) moieties) are described. nature heteroatom (S or Se) in fragment has no effect on maxima absorption bands (λICT), whereas a change position heteroatoms dithiole moiety from 1,3 to 1,2 leads substantial bathochromic shift λICT. Solvatochromism, thermochromism, negative halochromism these...

10.1021/jo990100r article EN The Journal of Organic Chemistry 1999-08-25

The synthesis and physical properties of a series novel fluorene π-electron acceptors (7−9) are described. Cyclic voltammograms 7 8 exhibit three separate reversible (or quasi-reversible) one-electron redox waves, characteristic strong electron acceptors. Spectroelectrochemical experiments show the appearance in long-wavelength visible region absorption bands at appropriate potentials which were attributed to transformations A → A•- A2-. Charge-transfer complexation with N-propylcarbazole...

10.1021/jo9803481 article EN The Journal of Organic Chemistry 1998-08-20

A new sterically shielded carbene with branched aromatic substituents (9a) and two palladium halogenide complexes (11a,b) have been prepared. The single crystal X-ray structures of free 9a 10b 11a were determined. Very high catalytic efficiencies evident for the 11a,b when latter employed as catalysts hydrodechlorination chloroarenes p-dichlorobenzene hexachlorobenzene. When optimized, foregoing approach is significantly more effective than those currently known transition metal complexes....

10.1039/c4dt02908a article EN Dalton Transactions 2014-01-01

Abstract Due to population upsurge, pesticides (derivatives of organophosphorus acids included) find widespread use in agriculture. The toxicity and long-term environmental hazard such compounds require detailed studies on decomposition mechanisms the development efficient, readily available, inexpensive systems for their decontamination. A simple straightforward method involves reactions with nucleophiles. Studies reactivity "normal" α-nucleophiles toward electron-deficient centers allowed...

10.1351/pac200880071381 article EN Pure and Applied Chemistry 2008-01-01

The new sterically shielded 1,3,4-trisubstituted 1,2,4-triazol-5-ylidenes 8b–d were synthesized by a three step method starting from 2-phenyl-1,3,4-oxadiazole. syntheses of palladium complexes 9a–d and 10a–d (including the derivatives 9c,d 10a–d) carried out via reactions stable carbenes 8a–d with halogenide salts in THF or toluene solution. Complexes found to be excellent catalysts for reductive dechlorination (hydrodechlorination) p-dichlorobenzene. structures 8c, 9a,b, 10a determined...

10.1039/c4dt01353k article EN Dalton Transactions 2014-01-01

Strong intramolecular charge transfer (ICT) in fluorenes 2 and 3 from a donor amino group to acceptor fluorene moiety leads exceptionally easy rotation around the C(9)(α) bond that has been registered by 1H NMR spectroscopy; single crystal X-ray analysis of 2i confirms changes numbers. Cyclic voltammetry (CV) compounds shows two closely spaced reversible single-electron reduction waves (in range –0.4 V –1.16 V, E1red½– E2red½⩽ 0.16 V) resulting radical anions dianions, respectively, third...

10.1039/p29960002453 article EN Journal of the Chemical Society. Perkin transactions II 1996-01-01

10.1023/a:1021699628721 article EN Russian Journal of Organic Chemistry 2002-01-01

Hypobromite ion, BrO-, is an effective α-nucleophile that reacts rapidly with activated phosphorus(V) and sulfonate esters. The parent acid oxidizes organic sulfides aryloxide ions. At pH 10−11 BrO- HOBr coexist in water are potentially useful as decontaminants of chlorosulfide blister agents the phosphonyl nerve agents. Bis(dialkylamide)hydrogen dibromobromates well characterized, stable, solids which form HOBr−BrO- mildly alkaline water. Reactions 4-nitrophenyl diethyl phosphate...

10.1021/jo0402430 article EN The Journal of Organic Chemistry 2004-11-10

Analysis of data for the transmission electronic effects in various biaryl systems has shown that introduction a bridge group between two benzene rings can both weaken and enhance interaction substituent functional centre located different rings. The nature mechanisms enhanced influences bridged systems, called positive effect (PBE), have been examined principal conditions manifestation PBE formulated. bibliography includes 192 references.

10.1070/rc1975v044n09abeh002372 article EN Russian Chemical Reviews 1975-09-30
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