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Marcin Kwit

Researcher Next ID · RN-041545

Researcher · Chemistry

Adam Mickiewicz University in Poznań

Poznan, Poland

Accepting doctoral researchersFunding unknown
Works count
481
Citation count
1,842
H-index
24
i10-index
56

Research interests

Chemistry
Materials Science
Crystallization and Solubility Studies
X-ray Diffraction in Crystallography
Molecular spectroscopy and chirality
Crystallography and molecular interactions
Axial and Atropisomeric Chirality Synthesis

Publications

  • Dehydration of a crystal hydrate at subglacial temperatures

    Nature · 2023 · 10.1038/s41586-023-05749-7

  • Sterically Crowded Trianglimines—Synthesis, Structure, Solid‐State Self‐Assembly, and Unexpected Chiroptical Properties

    Chemistry - An Asian Journal · 2018 · 10.1002/asia.201800938

  • One‐Step Construction of the Shape Persistent, Chiral But Symmetrical Polyimine Macrocycles

    The Chemical Record · 2018 · 10.1002/tcr.201800052

  • Chiral, triformylphenol-derived salen-type [4 + 6] organic cages

    Organic & Biomolecular Chemistry · 2016 · 10.1039/c6ob01429a

  • Unexpected narcissistic self-sorting at molecular and supramolecular levels in racemic chiral calixsalens

    CrystEngComm · 2016 · 10.1039/c6ce00256k

  • Dynamic Formation of Noncovalent Calixsalen Aggregates

    Chemistry - A European Journal · 2015 · 10.1002/chem.201500945

  • Mechanism and Enantioselectivity of [Zinc(diamine)(diol)]‐Catalyzed Asymmetric Hydrosilylation of Ketones: DFT, NMR and ECD Studies

    European Journal of Organic Chemistry · 2012 · 10.1002/ejoc.201200992

  • C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids

    Organic & Biomolecular Chemistry · 2011 · 10.1039/c0ob01192d

  • Convenient, enantioselective hydrosilylation of imines in protic media catalyzed by a Zn-trianglamine complex

    Organic & Biomolecular Chemistry · 2011 · 10.1039/c1ob05074e

  • Circular dichroism, optical rotation and absolute configuration of 2-cyclohexenone-cis-diol type phenol metabolites: redefining the role of substituents and 2-cyclohexenone conformation in electronic circular dichroism spectra

    Organic & Biomolecular Chemistry · 2010 · 10.1039/c0ob00422g

  • Convenient Enantioselective Hydrosilylation of Ketones Catalyzed by Zinc‐Macrocyclic Oligoamine Complexes

    Advanced Synthesis & Catalysis · 2009 · 10.1002/adsc.200800801

  • Density Functional Theory Calculations of the Optical Rotation and Electronic Circular Dichroism: The Absolute Configuration of the Highly Flexible trans-Isocytoxazone Revised

    The Journal of Organic Chemistry · 2009 · 10.1021/jo901175s

  • Lewis Acid-Catalyzed One-Pot, Three-Component Route to Chiral 3,3‘-Bipyrroles

    Organic Letters · 2008 · 10.1021/ol800115p

  • Toluene Dioxygenase‐Catalyzed Synthesis of cis‐Dihydrodiol Metabolites from 2‐Substituted Naphthalene Substrates: Assignments of Absolute Configurations and Conformations from Circular Dichroism and Optical Rotation Measurements

    Chemistry - A European Journal · 2008 · 10.1002/chem.200801686

  • Chiral Macrocyclic Aliphatic Oligoimines Derived from trans‐1,2‐Diaminocyclohexane

    Chemistry - A European Journal · 2007 · 10.1002/chem.200700648

  • Determination of absolute configuration of conformationally flexible cis‐dihydrodiol metabolites: Effect of diene substitution pattern on the circular dichroism spectra and optical rotations

    Chirality · 2007 · 10.1002/chir.20471

  • Absolute Configuration of Conformationally Flexible cis‐Dihydrodiol Metabolites by the Method of Confrontation of Experimental and Calculated Electronic CD Spectra and Optical Rotations

    Chemistry - A European Journal · 2007 · 10.1002/chem.200601851

  • Synthesis, stereochemistry, and photochemical and thermal behaviour of bis-tert-butyl substituted overcrowded alkenes

    Organic & Biomolecular Chemistry · 2006 · 10.1039/b611070c

  • Synthesis, structure, and contrasting chiroptical properties of large trianglimine macrocycles

    Chirality · 2005 · 10.1002/chir.20119

  • Absolute Configuration, Conformation, and Circular Dichroism of Monocyclic Arene Dihydrodiol Metabolites: It is All Due to the Heteroatom Substituents

    Journal of the American Chemical Society · 2005 · 10.1021/ja042895b

  • RhombiminesCyclic Tetraimines of trans-1,2-Diaminocyclohexane Shaped by the Diaryl Ether Structural Motif

    The Journal of Organic Chemistry · 2005 · 10.1021/jo051687e

  • Trianglamines—Readily Prepared, Conformationally Flexible Inclusion‐Forming Chiral Hexamines

    Chemistry - A European Journal · 2005 · 10.1002/chem.200500887

  • Chiral calixsalen-type macrocycles from trans-1,2-diaminocyclohexane

    Tetrahedron Asymmetry · 2003 · 10.1016/s0957-4166(03)00130-7

  • Helicity Induction in a Bichromophore: A Sensitive and Practical Chiroptical Method for Absolute Configuration Determination of Aliphatic Alcohols

    Organic Letters · 2002 · 10.1021/ol0268079

  • Designing Large Triangular Chiral Macrocycles: Efficient [3 + 3] Diamine−Dialdehyde Condensations Based on Conformational Bias

    The Journal of Organic Chemistry · 2000 · 10.1021/jo000623v

Current projects

    No projects listed.