First example of peroxosolvate of iodine-containing organic molecule

Churakov A.V., Medved’ko A.V., Prikhodchenko P.V., Krut’ko D.P., Vatsadze S.Z.
Тип документаJournal Article
Дата публикации2021-05-01
Название журналаMendeleev Communications
ИздательElsevier
КвартильQ2
ISSN09599436, 1364551X
  • General Chemistry
Краткое описание
Six new bispidine-based bis-amides containing residues of haloacetic acids were synthesized and characterized by X-ray crystallography. The dissolution of iodine-containing compound in concentrated hydrogen peroxide afforded bispidine peroxosolvate, in which the peroxide molecules participated in two donor hydrogen bonds with carbonyl oxygen atoms of the distinct adjacent organic molecules thus forming cyclic motifs in crystals. This structure is a first example of peroxosolvate of iodine-containing organic molecule.
Пристатейные ссылки: 25
Цитируется в публикациях: 3
Bispidine-based bis-azoles as a new family of supramolecular receptors: the theoretical approach
Vatsadze S.Z., Medved’ko A.V., Bodunov A.A., Lyssenko K.A.
Q2 Mendeleev Communications 2020 цитирований: 9
Tricyclic derivatives of bispidine as AMPA receptor allosteric modulators
Lavrov M.I., Veremeeva P.N., Karlov D.S., Zamoyski V.L., Grigoriev V.V., Palyulin V.A.
Q2 Mendeleev Communications 2019 цитирований: 8
Synthesis of 3,7-diacyl-1,5-dimethyl-3,7-diazabicyclo[3.3.1]nonane derivatives as promising lipid bilayer modifiers
Veremeeva P.N., Grishina I.V., Zaborova O.V., Averin A.D., Palyulin V.A.
Q2 Tetrahedron 2019 цитирований: 8
Cyclic dipeptide peroxosolvates: First direct evidence for hydrogen bonding between hydrogen peroxide and a peptide backbone
Churakov A.V., Grishanov D.A., Medvedev A.G., Mikhaylov A.A., Tripol'skaya T.A., Vener M.V., Navasardyan M.A., Lev O., Prikhodchenko P.V.
Q1 CrystEngComm 2019 цитирований: 9
Supramolecular organogels based on N-benzyl, N′-acylbispidinols
Medved’ko A., Dalinger A., Nuriev V., Semashko V., Filatov A., Ezhov A., Churakov A., Howard J., Shiryaev A., Baranchikov A., Ivanov V., Vatsadze S.
Q1 Nanomaterials 2019 цитирований: 10
Open Access
Open access
Pharmaceutical solvate formation for the incorporation of the antimicrobial agent hydrogen peroxide
Kersten K.M., Breen M.E., Mapp A.K., Matzger A.J.
Q1 Chemical Communications 2018 цитирований: 7
Hydrogen Peroxide Insular Dodecameric and Pentameric Clusters in Peroxosolvate Structures
Grishanov D.A., Navasardyan M.A., Medvedev A.G., Lev O., Prikhodchenko P.V., Churakov A.V.
Q1 Angewandte Chemie - International Edition 2017 цитирований: 16
Syntheses, structures, and stabilities of aliphatic and aromatic fluorous iodine(I) and iodine(III) compounds: the role of iodine Lewis basicity
Mukherjee T., Biswas S., Ehnbom A., Ghosh S.K., El-Zoghbi I., Bhuvanesh N., Bazzi H.S., Gladysz J.A.
Q2 Beilstein Journal of Organic Chemistry 2017 цитирований: 4
Open Access
Open access
Piperazine-Based N4-Type 16-Membered Macroheterocycles and Their Nickel(II) Complexes
Vatsadze S.Z., Krut’ko D.P., Blake A.J., Mountford P.
Q4 Macroheterocycles 2017 цитирований: 2
Open Access
Open access
Peroxosolvates: Formation criteria, H2O2 hydrogen bonding, and isomorphism with the corresponding hydrates
Chernyshov I.Y., Vener M.V., Prikhodchenko P.V., Medvedev A.G., Lev O., Churakov A.V.
Q1 Crystal Growth and Design 2017 цитирований: 41
Copper-Bispidine Complexes: Synthesis and Complex Stability Study
Medved’ko A.V., Egorova B.V., Komarova A.A., Rakhimov R.D., Krut’ko D.P., Kalmykov S.N., Vatsadze S.Z.
Q1 ACS Omega 2016 цитирований: 18
Open Access
Open access
Pharmaceutical cocrystals: walking the talk
Bolla G., Nangia A.
Q1 Chemical Communications 2016 цитирований: 273
Conformational Study of N,N′-Diacyl Bispidines and Dioxo Bis-bispidines: Planar Chirality and Molecular Switching
Wang Z., Islam M.J., Vukotic V.N., Revington M.J.
Q1 Journal of Organic Chemistry 2016 цитирований: 7
Bispidine as a Privileged Scaffold
Tomassoli I., Gündisch D.
Q2 Current Topics in Medicinal Chemistry 2016 цитирований: 30
Метрики
Поделиться
Цитировать
ГОСТ |
Цитировать
1. Churakov A.V. и др. First example of peroxosolvate of iodine-containing organic molecule // Mendeleev Communications. 2021. Т. 31. № 3. С. 352–355.
RIS |
Цитировать

TY - JOUR

DO - 10.1016/j.mencom.2021.04.023

UR - http://dx.doi.org/10.1016/j.mencom.2021.04.023

TI - First example of peroxosolvate of iodine-containing organic molecule

T2 - Mendeleev Communications

AU - Churakov, Andrei V.

AU - Medved’ko, Aleksei V.

AU - Prikhodchenko, Petr V.

AU - Krut’ko, Dmitry P.

AU - Vatsadze, Sergey Z.

PY - 2021

DA - 2021/05

PB - Elsevier BV

SP - 352-355

IS - 3

VL - 31

SN - 0959-9436

ER -

BibTex |
Цитировать

@article{2021,

doi = {10.1016/j.mencom.2021.04.023},

url = {https://doi.org/10.1016%2Fj.mencom.2021.04.023},

year = 2021,

month = {may},

publisher = {Elsevier {BV}},

volume = {31},

number = {3},

pages = {352--355},

author = {Andrei V. Churakov and Aleksei V. Medved'ko and Petr V. Prikhodchenko and Dmitry P. Krut'ko and Sergey Z. Vatsadze},

title = {First example of peroxosolvate of iodine-containing organic molecule}

}

MLA
Цитировать
Churakov, Andrei V. et al. “First Example of Peroxosolvate of Iodine-Containing Organic Molecule.” Mendeleev Communications 31.3 (2021): 352–355. Crossref. Web.