Loading [MathJax]/jax/output/SVG/config.js
Mendeleev Communications
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Mendeleev Commun.:
Year:
Volume:
Issue:
Page:
Find






Personal entry:
Login:
Password:
Save password
Enter
Forgotten password?
Register


Mendeleev Communications, 1996, Volume 6, Issue 2, Pages 60–62
DOI: https://doi.org/10.1070/MC1996v006n02ABEH000580
(Mi mendc4914)
 

This article is cited in 14 scientific papers (total in 14 papers)

Infrared spectra of amino acid and peptide monoderivatives of [60]fullerene and their methyl esters

Z. S. Klemenkova, V. S. Romanova, V. A. Tsyryapkin, V. E. Muradan, Z. N. Parnes, B. V. Lokshin, M. E. Vol'pin

A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract: IR spectra (4000–400 cm–1) of [60]fullerene monoderivatives of amino acids and dipeptides and several of their methyl esters have been found to differ strongly from those of starting compounds, in that none of them contained the characteristic modes of free C60 but instead displayed several new absorptions which indicate the presence of amino acid and peptide moieties in the [60]fullerene derivative molecules, these fragments being in a zwitterion form in most cases.
Document Type: Article
Language: English


Citation: Z. S. Klemenkova, V. S. Romanova, V. A. Tsyryapkin, V. E. Muradan, Z. N. Parnes, B. V. Lokshin, M. E. Vol'pin, “Infrared spectra of amino acid and peptide monoderivatives of [60]fullerene and their methyl esters”, Mendeleev Commun., 6:2 (1996), 60–62
Linking options:
  • https://www.mathnet.ru/eng/mendc4914
  • https://www.mathnet.ru/eng/mendc/v6/i2/p60
  • This publication is cited in the following 14 articles:
    1. Konstantin A. Kochetkov, Valentina S. Romanova, Nadezhda Yu Shepeta, “Synthesis of hybrid nanostructures based on e -carboxy-dihydroxycobinamide and N -(monohydrofullerenyl)- l -fluorophenylalanines”, Fullerenes, Nanotubes and Carbon Nanostructures, 32:9 (2024), 836  crossref
    2. O. V. Yamskova, D. V. Kurilov, V. A. Volkov, M. V. Voronkov, I. V. Zavarzin, “C60 Fullerene Amino Acid Derivatives: Synthesis and Biomedical Applications (A Review)”, Russ J Bioorg Chem, 49:5 (2023), 930  crossref
    3. O. V. Yamskova, D. V. Kurilov, V. A. Volkov, M. V. Voronkov, I. V. Zavarzin, “C<sub>60</sub> Fullerene Amino Acid Derivatives: Synthesis and Biomedical Applications”, RUBI, 49:5 (2023), 455  crossref
    4. A.Yu. Belik, A.Yu. Rybkin, N.S. Goryachev, A.P. Sadkov, N.V. Filatova, A.G. Buyanovskaya, V.N. Talanova, Z.S. Klemenkova, V.S. Romanova, M.O. Koifman, A.A. Terentiev, A.I. Kotelnikov, “Nanoparticles of water-soluble dyads based on amino acid fullerene C60 derivatives and pyropheophorbide: Synthesis, photophysical properties, and photodynamic activity”, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 260 (2021), 119885  crossref
    5. Yasaman Ghabdian, Azade Taheri, Ali Jahanian-Najafabadi, “Development of novel topical formulation from fullerene with antibacterial activity against Propionibacterium acnes”, Fullerenes, Nanotubes and Carbon Nanostructures, 29:2 (2021), 163  crossref
    6. N. A. Charykov, V. A. Keskinov, A. V. Petrov, “Adducts of Lower Fullerenes and Amino Acids: Synthesis, Identification, and Quantum-Mechanical Modeling of Their Physicochemical Properties”, Russ. J. Phys. Chem., 95:12 (2021), 2359  crossref
    7. Yang-Rong Yao, Olivia Fernandez-Delgado, Luis Echegoyen, Handbook of Carbon-Based Nanomaterials, 2021, 19  crossref
    8. V. S. Romanova, N. Yu. Shepeta, Z. S. Klemenkova, K. A. Kochetkov, “Catalytically active hybrid complex of fullerene C60 and vitamine B12”, Mendeleev Commun., 31:6 (2021), 844–846  mathnet  crossref
    9. Pauline Minois, Jérôme Bayardon, Rita Meunier-Prest, Sylvain Jugé, “[60]Fullerene l-Amino Acids and Peptides: Synthesis under Phase-Transfer Catalysis Using a Phosphine–Borane Linker. Electrochemical Behavior”, J. Org. Chem., 82:21 (2017), 11358  crossref
    10. Andrew R. Barron, “[60]Fullerene-peptides: bio-nano conjugates with structural and chemical diversity”, Journal of Enzyme Inhibition and Medicinal Chemistry, 31:sup1 (2016), 164  crossref
    11. R. A. Kotel'nikova, V. V. Grigoriev, A. V. Smolina, I. I. Faingold, D. V. Mishchenko, G. I. Van'kin, V. L. Zamoiskii, D. A. Poletaeva, N. A. Markova, V. S. Romanova, A. I. Kotel'nikov, G. Aliev, S. O. Bachurin, “Design of a hybrid nanostructure based on fullerene C60 and biologically active substance for modeling physiological properties of compounds”, Russ Chem Bull, 63:10 (2014), 2375  crossref
    12. L. B. Piotrovskii, “Fullerenes in the drug design”, Nanotechnol Russia, 4:9-10 (2009), 541  crossref
    13. M. E. Vol'pin, Z. N. Parnes, V. S. Romanova, “Amino acid and peptide derivatives of fullerene”, Russ Chem Bull, 47:5 (1998), 1021  crossref
    14. G. I. Timofeeva, E. F. Kuleshova, V. S. Romanova, “Dependence of the degree of association of water-soluble amino acid and peptide derivatives of fullerene[60] on pH and the ionic strength of a solution”, Russ Chem Bull, 46:3 (1997), 472  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Mendeleev Communications
    Statistics & downloads:
    Abstract page:27
    Full-text PDF :8
     
      Contact us:
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025