Firudin I. Guseinov

ORCID: 0000-0002-6769-0232
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Synthesis and Reactivity of Sulfur-Containing Compounds
  • Synthesis and Reactions of Organic Compounds
  • Organophosphorus compounds synthesis
  • Chemical Synthesis and Reactions
  • Fluorine in Organic Chemistry
  • Phosphorus compounds and reactions
  • Synthesis and Biological Evaluation
  • Synthesis and Characterization of Heterocyclic Compounds
  • Crystal structures of chemical compounds
  • Synthesis of heterocyclic compounds
  • Synthesis and biological activity
  • Metal-Organic Frameworks: Synthesis and Applications
  • Vanadium and Halogenation Chemistry
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Structural and Chemical Analysis of Organic and Inorganic Compounds
  • Polyoxometalates: Synthesis and Applications
  • Crystallography and molecular interactions
  • Organic Chemistry Cycloaddition Reactions
  • Synthesis and Catalytic Reactions
  • Sulfur-Based Synthesis Techniques
  • Synthesis and Reactivity of Heterocycles
  • Chemical Synthesis and Analysis
  • Chemical Reaction Mechanisms

A. N. Kosygin Moscow State Textile University
2021-2025

N.D. Zelinsky Institute of Organic Chemistry
2017-2025

National University of Science and Technology
2016-2020

Lomonosov Moscow State University
2016-2018

Kazan State Technological University
2002-2017

National University of Science and Technology
2017

Immanuel Kant Baltic Federal University
2016-2017

Kazan Federal University
1998

Five isostructural lanthanide MOFs, [Ln(1κOO',2κO'',3κO''',4κO''''-μ4-L)(NO3)(DMF)2]n·n(DMF) {Ln = La3+ (1), Ce3+ (2), Nd3+ (3), Sm3+ (4) and Dy3+ (5); L 5-[2-{2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene}hydrazinyl]isophthalate; DMF N,N'-dimethyl formamide}, based on dicarboxyl-functionalized arylhydrazone of barbituric acid were synthesized under solvothermal conditions. They characterized by elemental analysis, FT-IR spectroscopy, thermogravimetric X-ray diffraction analyses. Crystal...

10.1039/c7dt01056g article EN Dalton Transactions 2017-01-01

Two known iron(iii) complexes, [Fe(H2O)3(L1)]·xH2O (x = 4 (1), 5 (2)) and [Fe(H2O)3(L2)]·3H2O (3), bearing the basic forms of 5-chloro-3-(2-(4,4-dimethyl-2,6-dioxocyclohexylidene)hydrazinyl)-2-hydroxybenzenesulfonic acid (H3L1) 3-(2-(2,4-dioxopentan-3-ylidene)hydrazinyl)-2-hydroxy-5-nitrobenzenesulfonic (H3L2), were prepared used as homogeneous catalysts for cyanosilylation a variety aldehydes with trimethylsilyl cyanide leading to corresponding cyanohydrin ethers. High yield (up 98 %) was...

10.1071/ch17595 article EN Australian Journal of Chemistry 2018-01-01

The asymmetric units of the compounds, C 8 H 5 BrCl 2 O (I), and 9 Br (II), contain two one crystallographically independent molecules, respectively. In compound planar rings are oriented at a dihedral angle 13.23 (8)°. crystals both intermolecular C—H...O hydrogen bonds link molecules into infinite chains along b -axis direction. crystal there π–π interactions between centroids parallel with centroid-to-centroid distances 3.5974 (14), 3.6178 (16) 3.9387 Å while neither nor C—H... π(ring)...

10.1107/s205698902500012x article EN cc-by Acta Crystallographica Section E Crystallographic Communications 2025-01-14

The asymmetric unit of the title compound, C9H10N2S, contains two crystallographically independent, almost planar, mol-ecules. In crystal, inter-mole-cular N-H⋯S hydrogen bonds link mol-ecules into pseudocentrosymmetric dimers, enclosing R 2 2(8) ring motifs. There are mutual π-π inter-actions between five- and six-membered rings each independent mol-ecule in chosen unit, with centroid-to-centroid distances 3.6685 (12) 3.7062 Å. A weak C-H⋯π(ring) inter-action is also observed. bonds,...

10.1107/s2056989025000519 article EN cc-by Acta Crystallographica Section E Crystallographic Communications 2025-01-28

The title compound, C 23 H 16 ClF 3 N 2 , was synthesized from 3-(trifluoromethyl)-1 -pyrazole and chloro(4-chlorophenyl)methylene)dibenzene. structure features intramolecular (Ph)C—H...N intermolecular (Ph)C—H...F hydrogen bonds, as well C—H...π-ring interactions between the phenyl pyrazole rings.

10.1107/s2056989025001185 article EN cc-by Acta Crystallographica Section E Crystallographic Communications 2025-02-18

The title compounds, C 10 H 9 Cl 2 FN O 3 , ( I ), and 11 12 N II are α,α-dihalo-β-diketone urea derivatives, which contain 4-fluorophenyl p -tolyl groups, respectively. conformation about the —C Cl2 —N u (O = keto, dichloro, urea) bond is anti in ) gauche ). In crystals of both O—H...O hydrogen bonds generate inversion dimers linked into (100) layers by N—H...O bonds. Hirshfeld surface analyses crystal structures indicate that most important contributions for packings from H...O/O...H...

10.1107/s2056989025004359 article EN cc-by Acta Crystallographica Section E Crystallographic Communications 2025-05-20

In the title compound, C 6 H 4 BrF 3 N O 2 , oxadiazole ring is essentially planar with a maximum deviation of 0.003 (2) Å. crystal, molecular pairs are connected by N—H...N hydrogen bonds, forming dimers an R (8) motif. The linked into layers parallel to (10\overline{4}) plane N—H...O bonds. addition, C—O...π and C—Br...π interactions connect molecules, three-dimensional network. F atoms trifluoromethyl group disordered over two sites in 0.515 (6): 0.485 (6) ratio. intermolecular crystal...

10.1107/s2056989024004080 article EN cc-by Acta Crystallographica Section E Crystallographic Communications 2024-05-10

Reaction of 2-chloro-2-(diethoxymethyl)-3-substitutedoxirane or 1-chloro-1-(substituted) -3,3-diethoxypropan-2-one with pyridine-2-thiol in EtOH at 25 °C yields 3-(diethoxymethyl)-3-hydroxy-2-substituted-2,3-dihydrothiazolo[3,2-a]pyridin-4-ium chlorides, which subsequently, MeCN 85°C, transforms into ring-opening products, 2-((2-carboxy-1-(substituted) -2-hydroxyethyl)thio)pyridin-1-ium chlorides. The tetrel (C···O) and chalcogen (S···O) bonds are found the structures 5 6, respectively....

10.3390/cryst7110327 article EN cc-by Crystals 2017-10-28

10.1023/a:1016004027096 article Chemistry of Heterocyclic Compounds 2002-01-01
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