K. S. Shibaeva

ORCID: 0000-0002-7948-206X
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About
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Research Areas
  • Supramolecular Chemistry and Complexes
  • Molecular Sensors and Ion Detection
  • Organophosphorus compounds synthesis
  • Supramolecular Self-Assembly in Materials
  • Advanced NMR Techniques and Applications
  • Chemical Synthesis and Analysis
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Advanced biosensing and bioanalysis techniques
  • Mass Spectrometry Techniques and Applications
  • Chemical Synthesis and Characterization
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Radical Photochemical Reactions
  • Nanoparticle-Based Drug Delivery
  • Protein Structure and Dynamics
  • Protein Interaction Studies and Fluorescence Analysis
  • Enzyme Structure and Function
  • Hemoglobin structure and function
  • Porphyrin and Phthalocyanine Chemistry
  • Lanthanide and Transition Metal Complexes
  • Conducting polymers and applications
  • Molecular spectroscopy and chirality
  • Nanoplatforms for cancer theranostics
  • Synthesis and Characterization of Heterocyclic Compounds

Kazan Federal University
2016-2024

For the first time, a series of catechol-containing Schiff bases, tetrasubstituted at lower rim thiacalix[4]arene derivatives in three stereoisomeric forms, cone, partial and 1,3-alternate, were synthesized. The structure obtained compounds was proved by modern physical methods, such as NMR, IR spectroscopy, HRMS. Selective recognition (Kb difference orders magnitude) copper (II) cation d-metal cations (Cu2+, Ni2+, Co2+, Zn2+) shown UV-vis spectroscopy. Copper ions are coordinated nitrogen...

10.3390/molecules26082334 article EN cc-by Molecules 2021-04-17

Amyloid fibroproliferation leads to organ damage and is associated with a number of neurodegenerative diseases affecting populations worldwide. There are several ways protect against fibril formation, including inhibition. A variety organic compounds based on molecular recognition amino acids within the protein have been proposed for design such inhibitors. However, role macrocyclic compounds, i.e., thiacalix[4]arenes, in inhibiting fibrillation still almost unknown. In present work, use...

10.3390/ijms25094721 article EN International Journal of Molecular Sciences 2024-04-26

The search for new ways to obtain analogues of the well-known Methylene Blue dye is an important synthetic task. Herein, we proposed and developed approach synthesis 3-N'-arylaminophenothiazines asymmetrical 3,7-di(N'-arylamino)phenothiazines. This included optimization strategy by quantification analysis positive charge distribution in cation 3-N'-arylaminophenothiazine derivative. obtained experimental data are confirmed DFT studies. Two routes phenothiazine diarylamino derivatives were...

10.3390/molecules27093024 article EN cc-by Molecules 2022-05-08

GRAPHICAL ABSTRACTSynthesis of the monosubstituted pillar[5]arenes with 1-aminophosphonate fragmentAll authorsA.A. Nazarova, K.S. Shibaeva & I.I. Stoikovhttps://doi.org/10.1080/10426507.2016.1216420Published online:10 August 2016

10.1080/10426507.2016.1216420 article EN Phosphorus, sulfur, and silicon and the related elements 2016-08-10

GRAPHICAL ABSTRACTSynthesis of p-tert-butylthiacalix[4]arene derivatives with 1-aminobis(methylenephosphonic acid) fragments by Moedritzer-Irani reactionAll authorsK. S. Shibaeva, A. Nazarova & I. Stoikovhttps://doi.org/10.1080/10426507.2016.1216421Published online:10 August 2016

10.1080/10426507.2016.1216421 article EN Phosphorus, sulfur, and silicon and the related elements 2016-08-10

Selective sensors for the detection and quantification of Cu(II) ions are actively used to investigate in vivo conditions Wilsons Menkes diseases at cellular level. Such must have a high specificity this cation as well low toxicity. A synthetic approach preparation selective cations based on p-tert-butylthiacalix[4]arenes modified with 3,5-dimethylpyrazole moieties cone, partial cone 1,3-alternate stereoisomeric forms was developed. The obtained compounds were characterized by single-crystal...

10.15826/chimtech.2024.11.4.18 article EN cc-by Chimica Techno Acta 2024-11-27
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