Faculty

Institution

Unit

Venue

Mikhail V. Barybin

Professor

University of Kansas

Affiliations

College of Liberal Arts & Sciences

Chemistry

Mikhail V. Barybin is currently serving as a Chemistry Professor at University of Kansas.

Honors

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Experiences

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Education

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Mikhail V. Barybin

University of Kansas

Professor

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chemistry coordination chemistry inorganic chemistry materials science transition metal chemistry chemical synthesis organometallic chemistry organic synthesis organic chemistry inorganic synthesis biophysics material chemistry chemical engineering chemical sciences molecular structure structural chemistry redox chemistry structural characterizations homoleptic complexes self-assembly surface science redox biology surface chemistry synthetic chemistry electronic structure surface nanotechnology surface modification surface functionalization organic electronics stereoselective synthesis supramolecular assemblies supramolecular chemistry heterobimetallic complexation carbonyl chemistry magnetism laboratory investigation electronic materials biological chemistry condensed matter additive manufacturing plasma chemistry tribology composite science molecular science inorganic materials organic material chemistry biological inorganic chemistry molecular chemistry infrared spectroscopy lead identification functional modification heterocyclic texture analysis surface processing plasma processing molecular design crystal structures structure elucidation structure determination trinuclear molecular wire phthalocyanine motifs electronic properties first conventional syntheses structural characterization mm quadruple bonds long-range electronic coupling amidoximato ligand homoleptic carbonyl trifluorophosphane niobates homoleptic isocyanidemetalates organometallic isocyanocyclopentadienides organometallic catalysis

Notable Scholarly Works

Notable Federal Grants

Collaborators

Tuning the Redox Profile of the 6,6′-Biazulenic Platform Through Functionalization Along Its Molecular Axis. Chemical Communications (2024)

Shaun R. KelseyGeorgii GriaznovAndrew D. SpaethDaron E. JanzenJustin T. DouglasWard H. ThompsonMikhail V. Barybin

redox chemistrychemistrychemical synthesismedicinal chemistryredox biologypharmacologyredox profilemolecular axis

Ccdc 2157502: Experimental Crystal Structure Determination. The Cambridge Structural Database (2023)

Rao, YuPalumbo, Chad T.Venkatesh, AmritKeener, MeganStevanato, GabrieleChauvin, Anne-SophieMenzildjian, GeorgesKuzin, SergeiYulikov, MaximJeschke, GunnarLesage, AnneMazzanti, MarinellaEmsley, Lyndon

biophysicschemistrycrystal diffraction studycrystal engineeringcrystal researchcrystallographycrystal structuresccdc 2157502structure elucidationstructure determinationchemical structuredeposited datasetstructural chemistry

Homoleptic Complexes of Isocyano- and Diisocyanobiazulenes With a 12-Electron, Ligand-Based Redox Capacity. Dalton Transactions (2023)

Patrick T. ConnellyJason C. ApplegateDavid A. MaldonadoMonisola K. OkeowoWade C. HenkeAllen G. OliverCindy L. BerrieMikhail V. Barybin

homoleptic complexesredox chemistrychemical synthesismaterial chemistrymaterials sciencecoordination chemistry

Tuning π-Acceptor/σ-Donor Ratio of the 2-Isocyanoazulene Ligand: Non-Fluorinated Rival of Pentafluorophenyl Isocyanide and Trifluorovinyl Isocyanide Discovered. Molecules (2021)

Mason D. HartJohn J. MeyersZachary A. WoodToshinori NakakitaJason C. ApplegateNathan R. EricksonNikolay N. GerasimchukMikhail V. Barybin

chemistryorganic chemistrylead identificationchemical synthesisorganic synthesisnon-fluorinated rivalfunctional modificationcoordination chemistrytrifluorovinyl isocyanideheterocyclicpentafluorophenyl isocyanide

Quantitative Texture Analysis of a Hydroxyapatite Coatings Plasma-Sprayed on Titanium Substrates at Different Temperatures. Industrial laboratory Diagnostics of materials (2020)

V. F. ShamrayV. N. SerebryanyA. S. KolyanovaV. I. KalitaV. S. KomlevS. M. BarinovD. I. KomlevM. V. Barybin

materials engineeringmaterials sciencedifferent temperaturesmechanical engineeringsurface scienceadvanced materialstexture analysisbiomedical engineeringtitanium substratesadditive manufacturingplasma chemistrysurface processingtribologycharacterization (materials science)surface nanotechnologycomposite sciencesurface modificationcoatingsquantitative texture analysishydroxyapatite coatingsplasma processing

Positional Isomers of Isocyanoazulenes as Axial Ligands Coordinated to Ruthenium(II) Tetraphenylporphyrin: Fine-Tuning Redox and Optical Profiles. Inorganic Chemistry (2019)

Mahtab Fathi-RasekhGregory T. RohdeMason D. HartToshinori NakakitaYuriy V. ZatsikhaRashid R. ValievMikhail V. BarybinVictor N. Nemykin

redox chemistryinorganic chemistryfine-tuning redoxpositional isomersoptical profilesaxial ligandscoordination chemistrytransition metal chemistry

Dynamics of Electron Transfer in Azulene-Based Self-Assembled Monolayers. The Journal of Physical Chemistry C (2017)

Tobias WächterKolbe J. ScheetzAndrew D. SpaethMikhail V. BarybinMichael Zharnikov

biophysicsazulene-based self-assembled monolayerscondensed matterelectron transfermaterials sciencephysical chemistryapplied physicsorganic electronics

First π-Linker Featuring Mercapto and Isocyano Anchoring Groups Within the Same Molecule: Synthesis, Heterobimetallic Complexation and Self-Assembly on Au(111). Chemical Science (2015)

Jason C. ApplegateMonisola K. OkeowoNathan R. EricksonBrad M. NealCindy L. BerrieNikolay N. GerasimchukMikhail V. Barybin

chemistrychemical synthesisheterobimetallic complexationself-assemblychemical sciencessame moleculeorganic synthesiscoordination chemistry

Probing Electronic Communications in Heterotrinuclear Fe–Ru–Fe Molecular Wires Formed by Ruthenium(II) Tetraphenylporphyrin and Isocyanoferrocene or 1,1′-Diisocyanoferrocene Ligands. Inorganic Chemistry (2015)

Victor N. NemykinSemyon V. DudkinMahtab Fathi-RasekhAndrew D. SpaethHannah M. RhodaRodion V. BelosludovMikhail V. Barybin

inorganic chemistryelectronic communicationselectrical engineeringcoordination chemistry

Cheminform Abstract: Remote Induction of Stereoselective 1,2‐Addition of Aryl Grignard Reagents to β‐Sulfinyl Enones.. ChemInform (2014)

Toshinori NakakitaMotofumi MiuraMasaharu ToriyamaShigeyasu MotohashiMikhail V. Barybin

chemistryorganic chemistryb-sulfinyl enoneschemical synthesisaryl grignard reagentsorganic synthesisremote inductionstereoselective synthesischeminform abstract

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Mikhail V. Barybin

Professor

University of Kansas

Affiliations

College of Liberal Arts & Sciences

Chemistry

Mikhail V. Barybin is currently serving as a Chemistry Professor at University of Kansas.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Mikhail V. Barybin

University of Kansas

Professor

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Tuning the Redox Profile of the 6,6′-Biazulenic Platform Through Functionalization Along Its Molecular Axis. Chemical Communications (2024)

Shaun R. KelseyGeorgii GriaznovAndrew D. SpaethDaron E. JanzenJustin T. DouglasWard H. ThompsonMikhail V. Barybin

redox chemistrychemistrychemical synthesismedicinal chemistryredox biologypharmacologyredox profilemolecular axis

Ccdc 2157502: Experimental Crystal Structure Determination. The Cambridge Structural Database (2023)

Rao, YuPalumbo, Chad T.Venkatesh, AmritKeener, MeganStevanato, GabrieleChauvin, Anne-SophieMenzildjian, GeorgesKuzin, SergeiYulikov, MaximJeschke, GunnarLesage, AnneMazzanti, MarinellaEmsley, Lyndon

Homoleptic Complexes of Isocyano- and Diisocyanobiazulenes With a 12-Electron, Ligand-Based Redox Capacity. Dalton Transactions (2023)

Patrick T. ConnellyJason C. ApplegateDavid A. MaldonadoMonisola K. OkeowoWade C. HenkeAllen G. OliverCindy L. BerrieMikhail V. Barybin

homoleptic complexesredox chemistrychemical synthesismaterial chemistrymaterials sciencecoordination chemistry

Tuning π-Acceptor/σ-Donor Ratio of the 2-Isocyanoazulene Ligand: Non-Fluorinated Rival of Pentafluorophenyl Isocyanide and Trifluorovinyl Isocyanide Discovered. Molecules (2021)

Mason D. HartJohn J. MeyersZachary A. WoodToshinori NakakitaJason C. ApplegateNathan R. EricksonNikolay N. GerasimchukMikhail V. Barybin

Quantitative Texture Analysis of a Hydroxyapatite Coatings Plasma-Sprayed on Titanium Substrates at Different Temperatures. Industrial laboratory Diagnostics of materials (2020)

V. F. ShamrayV. N. SerebryanyA. S. KolyanovaV. I. KalitaV. S. KomlevS. M. BarinovD. I. KomlevM. V. Barybin

Positional Isomers of Isocyanoazulenes as Axial Ligands Coordinated to Ruthenium(II) Tetraphenylporphyrin: Fine-Tuning Redox and Optical Profiles. Inorganic Chemistry (2019)

Mahtab Fathi-RasekhGregory T. RohdeMason D. HartToshinori NakakitaYuriy V. ZatsikhaRashid R. ValievMikhail V. BarybinVictor N. Nemykin

redox chemistryinorganic chemistryfine-tuning redoxpositional isomersoptical profilesaxial ligandscoordination chemistrytransition metal chemistry

Dynamics of Electron Transfer in Azulene-Based Self-Assembled Monolayers. The Journal of Physical Chemistry C (2017)

Tobias WächterKolbe J. ScheetzAndrew D. SpaethMikhail V. BarybinMichael Zharnikov

biophysicsazulene-based self-assembled monolayerscondensed matterelectron transfermaterials sciencephysical chemistryapplied physicsorganic electronics

First π-Linker Featuring Mercapto and Isocyano Anchoring Groups Within the Same Molecule: Synthesis, Heterobimetallic Complexation and Self-Assembly on Au(111). Chemical Science (2015)

Jason C. ApplegateMonisola K. OkeowoNathan R. EricksonBrad M. NealCindy L. BerrieNikolay N. GerasimchukMikhail V. Barybin

chemistrychemical synthesisheterobimetallic complexationself-assemblychemical sciencessame moleculeorganic synthesiscoordination chemistry

Victor N. NemykinSemyon V. DudkinMahtab Fathi-RasekhAndrew D. SpaethHannah M. RhodaRodion V. BelosludovMikhail V. Barybin

inorganic chemistryelectronic communicationselectrical engineeringcoordination chemistry

Cheminform Abstract: Remote Induction of Stereoselective 1,2‐Addition of Aryl Grignard Reagents to β‐Sulfinyl Enones.. ChemInform (2014)

Toshinori NakakitaMotofumi MiuraMasaharu ToriyamaShigeyasu MotohashiMikhail V. Barybin

chemistryorganic chemistryb-sulfinyl enoneschemical synthesisaryl grignard reagentsorganic synthesisremote inductionstereoselective synthesischeminform abstract

1
2
3
4
5
10 / page

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organic chemistry

synthetic organic chemistry

Nicholas Leadbeater

Institution

University of Connecticut

radiofrequency heating

organic chemistry

Nathan D. Schley

Institution

Vanderbilt University

organometallic chemistry

coordination chemistry

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sustainable chemistry

multimetallic cooperativity

Michael G. Richmond

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University of North Texas

photocatalysis

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reactive intermediates

Daniel J. Mindiola

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University of Pennsylvania

chemical synthesis

organometallic synthesis

Russell P. Hughes

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Shao-Liang Zheng

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crystal research

materials science