Author

Sergey A. Pisarev

Observed names: Pisarev, S.A., Pisarev, Sergey, Pisarev, Sergey A., S. A. PISAREV, S. A. Pisarev, S.A. Pisarev, Sergei A. Pisarev, Sergey A. Pisarevd, Sergey Pisarev

Institution: Institute of Synthetic Polymeric Materials

Observed institutions: Russian Academy of Sciences, Lomonosov Moscow State University, Frumkin Institute of Physical Chemistry and Electrochemistry Russian Academy of Sciences, Institute of Synthetic Polymeric Materials, Institute of Physiologically Active Compounds

ORCID: 0000-0003-0262-4397

Observed ORCID: 0000-0003-0262-4397

OpenAlex ID: A5080314011

Self-assembly in double-tailed surfactants in dilute aqueous solutions

1995 · Tatiana F. Svitova, Yulia P. Smirnova, et al. · Colloids and Surfaces A Physicochemical and Engineering Aspects · 70

Palladium-containing hypercrosslinked polystyrene as an easy to prepare catalyst for Suzuki reaction in water and organic solvents

2009 · Sergey E. Lyubimov, Andrei A. Vasil’ev, et al. · Reactive and Functional Polymers · 62

Atomic Charges via Electronegativity Equalization: Generalizations and Perspectives

2006 · Alexander A. Oliferenko, Sergei A. Pisarev, et al. · Advances in quantum chemistry · 34

A novel highly efficient nanostructured organosilicon luminophore with unusually fast photoluminescence

2016 · T. Yu. Starikova, N. M. Surin, et al. · Journal of Materials Chemistry C · 29

Influence of the structure of electron-donating aromatic units in organosilicon luminophores based on 2,1,3-benzothiadiazole electron-withdrawing core on their absorption-luminescent properties

2018 · Maxim S. Skorotetcky, Evgeniya D. Krivtsova, et al. · Dyes and Pigments · 28

Fast tools for calculation of atomic charges well suited for drug design

2008 · D.A. Shulga, A.A. Oliferenko, et al. · SAR and QSAR in environmental research · 22

Novel point charge models: reliable instruments formolecular electrostatic

2001 · Alexander A. Oliferenko, Vladimir A. Palyulin, et al. · Journal of Physical Organic Chemistry · 22

Highly soluble and thermally stable alkyl-free star-shaped D-π-A oligomer with electron-withdrawing phenyldicyanovinyl groups for organic photovoltaics

2017 · Yuriy N. Luponosov, Alexander N. Solodukhin, et al. · Organic Electronics · 21

Triphenylamine-based luminophores with different side and central aromatic blocks: Synthesis, thermal, photophysical and photochemical properties

2020 · Yuriy N. Luponosov, Alexander N. Solodukhin, et al. · Dyes and Pigments · 18

New highly cytotoxic organic and organometallic bexarotene derivatives

2017 · Yulia N. Nosova, Dmitry S. Karlov, et al. · Journal of Organometallic Chemistry · 18

Interaction of silver nanoparticles with ozone in aqueous solution

2011 · P. A. Morozov, E. V. Abkhalimov, et al. · Colloid Journal · 18

The “Hockey Sticks” Effect Revisited: The Conformational and Electronic Properties of 3,7-Dithia-1,5-diazabicyclo[3.3.1]nonane from the QTAIM Perspective

2011 · I. S. Bushmarinov, I. V. Fedyanin, et al. · The Journal of Physical Chemistry A · 17

Synthesis of polyvinylpyrrolidone and its nanosilver-based polymer composites in supercritical carbon dioxide

2010 · E. E. Said-Galiev, A. I. Stakhanov, et al. · Polymer Science Series B · 14

Ultrafast intramolecular energy transfer in a nanostructured organosilicon luminophore based on p -terphenyl and 1,4-bis(5-phenyloxazol-2-yl)benzene

2019 · Sergey A. Ponomarenko, Nikolay M. Surin, et al. · Journal of Materials Chemistry C · 13

Synthesis and photostability of 1,4-bis(5-phenyloxazol-2-yl)benzene (POPOP) structural isomers and their trimethylsilyl derivatives

2017 · Maxim S. Skorotetcky, Oleg V. Borshchev, et al. · Dyes and Pigments · 12

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Synthesis and photovoltaic effect in red/near-infrared absorbing A-D-A-D-A-type oligothiophenes containing benzothiadiazole and thienothiadiazole central units

2015 · Yuriy N. Luponosov, Jie Min, et al. · Journal of Photonics for Energy · 12

Crystals of Diphenyl-Benzothiadiazole and Its Derivative with Terminal Trimethylsilyl Substituents: Growth from Solutions, Structure, and Fluorescence Properties

2024 · Valery A. Postnikov, Nataliya I. Sorokina, et al. · ACS Omega · 11

Computational characterization of the glutamate receptor antagonist perampanel and its close analogs: density functional exploration of conformational space and molecular docking study

2019 · Abdul-Akim D. Guseynov, Sergey A. Pisarev, et al. · Journal of Molecular Modeling · 9

General Purpose Electronegativity Relaxation Charge Models Applied to CoMFA and CoMSIA Study of GSK‐3 Inhibitors

2011 · Daria A. Tsareva, Dmitry I. Osolodkin, et al. · Molecular Informatics · 9

p-Flurophenyldicyanovinyl as electron-withdrawing group for highly soluble and thermally stable donor–acceptor small molecules

2018 · Dmitry O. Balakirev, Yuriy N. Luponosov, et al. · Journal of Photonics for Energy · 8

Synthesis and Photophysical Properties of Novel Meta-Conjugated Organic Molecules with 1,3,5-Benzene Branching Units

2022 · Maxim S. Skorotetcky, Nikolay M. Surin, et al. · The Journal of Physical Chemistry B · 7

Lone pairs vs. covalent bonds: conformational effects in bicyclo[3.3.1]nonane derivatives

2018 · Sergey A. Pisarev, Dmitry A. Shulga, et al. · Structural Chemistry · 7

Multipole models of sulphur for accurate anisotropic electrostatic interactions within force fields

2017 · D. A. Shulga, O. I. Titov, et al. · SAR and QSAR in environmental research · 6

Structural and morphological changes induced by intense shock waves in carbon nanotubes

2008 · A. M. Molodets, A. A. Golyshev, et al. · Nanotechnologies in Russia · 6

Parameterization of empirical schemes of partial atomic charge calculation for reproducing the molecular electrostatic potential

2008 · D. A. Shulga, A. A. Oliferenko, et al. · Doklady Chemistry · 6

Works count: 52

Citation count: 518

H-index: 13

I10-index: 17