Open Access
Journal of Molecular Liquids, volume 327, pages 114806
Novel lactide derivatives of p-tert-butylthiacalix[4]arene: Directed synthesis and molecular recognition of catecholamines
Publication type: Journal Article
Publication date: 2021-04-01
Journal:
Journal of Molecular Liquids
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 6
ISSN: 01677322, 18733166
Materials Chemistry
Electronic, Optical and Magnetic Materials
Physical and Theoretical Chemistry
Spectroscopy
Atomic and Molecular Physics, and Optics
Condensed Matter Physics
Abstract
Three stereoisomeric forms of p-tert-butylthiacalix[4]arene (cone, partial cone, and 1,3-alternate conformations) have been proposed as macrocyclic scaffold to obtain dendrimer-like compounds. Modification of the macrocycle with fragments containing both amide and lactide groups made it possible to obtain original analogs of dendrimers with symmetric and asymmetric structures. These compounds are capable of binding catecholamines (dopamine, epinephrine, and norepinephrine). The influence of the macrocyclic platform conformation of the compounds obtained on the efficiency and selectivity of their complexation with catecholamines was established by UV–visible, fluorescence and NMR spectroscopy. It was found that the 1,3-alternate conformation of the macrocycle core was the most favorable for binding all the guests. In case of the cone conformation, selectivity of binding of epinephrine and norepinephrine was observed. Location of catecholamines in the resulting complexes against the macrocyclic platform affected the efficiency of interaction of the synthesized thiacalixarenes with guests.
Top-30
Citations by journals
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International Journal of Molecular Sciences
2 publications, 18.18%
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Pharmaceutics
2 publications, 18.18%
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Molecules
1 publication, 9.09%
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Russian Journal of Organic Chemistry
1 publication, 9.09%
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1 publication, 9.09%
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New Journal of Chemistry
1 publication, 9.09%
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Colloid Journal
1 publication, 9.09%
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1 publication, 9.09%
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Biosensors
1 publication, 9.09%
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Citations by publishers
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Multidisciplinary Digital Publishing Institute (MDPI)
7 publications, 63.64%
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Pleiades Publishing
2 publications, 18.18%
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Royal Society of Chemistry (RSC)
1 publication, 9.09%
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Elsevier
1 publication, 9.09%
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- We do not take into account publications without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Mostovaya O. A. et al. Novel lactide derivatives of p-tert-butylthiacalix[4]arene: Directed synthesis and molecular recognition of catecholamines // Journal of Molecular Liquids. 2021. Vol. 327. p. 114806.
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Mostovaya O. A., Padnya P. L., Shurpik D. N., Shiabiev I. E., Stoikov I. I., Padnya P., Shurpik D. N., Stoikov I. Novel lactide derivatives of p-tert-butylthiacalix[4]arene: Directed synthesis and molecular recognition of catecholamines // Journal of Molecular Liquids. 2021. Vol. 327. p. 114806.
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TY - JOUR
DO - 10.1016/j.molliq.2020.114806
UR - https://doi.org/10.1016/j.molliq.2020.114806
TI - Novel lactide derivatives of p-tert-butylthiacalix[4]arene: Directed synthesis and molecular recognition of catecholamines
T2 - Journal of Molecular Liquids
AU - Mostovaya, O A
AU - Padnya, P L
AU - Shurpik, D N
AU - Shiabiev, I E
AU - Stoikov, I I
AU - Padnya, Pavel
AU - Shurpik, Dmitriy N
AU - Stoikov, Ivan
PY - 2021
DA - 2021/04/01 00:00:00
PB - Elsevier
SP - 114806
VL - 327
SN - 0167-7322
SN - 1873-3166
ER -
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@article{2021_Mostovaya,
author = {O A Mostovaya and P L Padnya and D N Shurpik and I E Shiabiev and I I Stoikov and Pavel Padnya and Dmitriy N Shurpik and Ivan Stoikov},
title = {Novel lactide derivatives of p-tert-butylthiacalix[4]arene: Directed synthesis and molecular recognition of catecholamines},
journal = {Journal of Molecular Liquids},
year = {2021},
volume = {327},
publisher = {Elsevier},
month = {apr},
url = {https://doi.org/10.1016/j.molliq.2020.114806},
pages = {114806},
doi = {10.1016/j.molliq.2020.114806}
}