Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles.
Publication type: Journal Article
Publication date: 2011-10-11
scimago Q1
wos Q1
SJR: 0.958
CiteScore: 7.4
Impact factor: 4.7
ISSN: 00201669, 1520510X
PubMed ID:
21988373
Inorganic Chemistry
Physical and Theoretical Chemistry
Abstract
A series of heterocyclic compounds containing trivalent iodine, oxygen, and boron in a five-membered ring were prepared and structurally investigated by X-ray crystallography. 1-Chloro-4-fluoro-1H-1λ(3)-benzo[d][1,2,3]iodoxoborol-3-ol was synthesized by chlorination of 2-fluoro-6-iodophenylboronic acid followed by treatment of the intermediate iododichloride with water. 1-Acetoxy-4-fluoro-1H-1λ(3)-benzo[d][1,2,3]iodoxoborol-3-ol, 1-acetoxy-1H-1λ(3)-benzo[d][1,2,3]iodoxoborol-3-ol, and similar 1-substituted trifluoroacetate derivatives of benziodoxaborole were prepared the hypochlorite oxidation of 2-fluoro-6-iodophenylboronic acid or 2-iodophenylboronic acid in acetic or trifluoroacetic acid, respectively. 1-Acetoxy substituted benziodoxaborole can be further converted to the respective trifluoroacetate by treatment with trifluoroacetic acid or to the 1-hydroxy derivative by basic hydrolysis with aqueous NaHCO(3). X-ray structural studies of 1-chloro- and 1-trifluoroacetoxy substituted benziodoxaboroles 13, 17, and 18 have shown the presence of a planar five-membered heterocyclic ring with unusually short endocyclic I-O bond distance of 2.04-2.09 Å. Slow crystallization of 4-fluoro-1-trifluoroacetoxy-1H-1λ(3)-benzo[d][1,2,3]iodoxoborol-3-ol from methanol resulted in the formation of a tetrameric macrocyclic structure 21 resulting from self-assembly of the initially formed 4-fluoro-1,3-dimethoxy-1H-1λ(3)-benzo[d][1,2,3]iodoxoborol. Structural parameters of the five-membered iodoxoborol ring, such as the planar geometry and the short B-O and O-I bonds lengths in 13, 17, and 18 compared to those in 21 and known benziodoxoles are indicative of partially aromatic character of this ring. Density functional theory (DFT) predicted NIST (0) and NIST (1) indexes for 1-chloro- and 1-trifluoroacetoxy substituted benziodoxaboroles, however, are indicative of significantly lower aromaticity compared to the classic aromatic systems.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
|
|
|
Angewandte Chemie
2 publications, 8.33%
|
|
|
Angewandte Chemie - International Edition
2 publications, 8.33%
|
|
|
Organometallics
2 publications, 8.33%
|
|
|
Advances in Heterocyclic Chemistry
2 publications, 8.33%
|
|
|
Chemistry - A European Journal
1 publication, 4.17%
|
|
|
Chemistry of Heterocyclic Compounds
1 publication, 4.17%
|
|
|
Beilstein Journal of Organic Chemistry
1 publication, 4.17%
|
|
|
Molecules
1 publication, 4.17%
|
|
|
Structural Chemistry
1 publication, 4.17%
|
|
|
Inorganic Chemistry
1 publication, 4.17%
|
|
|
Chemical Reviews
1 publication, 4.17%
|
|
|
Annual Reports Section A (Inorganic Chemistry)
1 publication, 4.17%
|
|
|
Advanced Synthesis and Catalysis
1 publication, 4.17%
|
|
|
Journal of Organic Chemistry
1 publication, 4.17%
|
|
|
Russian Chemical Reviews
1 publication, 4.17%
|
|
|
1
2
|
Publishers
|
2
4
6
8
10
|
|
|
Wiley
10 publications, 41.67%
|
|
|
American Chemical Society (ACS)
5 publications, 20.83%
|
|
|
Elsevier
3 publications, 12.5%
|
|
|
Springer Nature
2 publications, 8.33%
|
|
|
Beilstein-Institut
1 publication, 4.17%
|
|
|
MDPI
1 publication, 4.17%
|
|
|
Royal Society of Chemistry (RSC)
1 publication, 4.17%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 4.17%
|
|
|
2
4
6
8
10
|
- We do not take into account publications without a DOI.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
24
Total citations:
24
Citations from 2024:
4
(16.67%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Nemykin V. V. et al. Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles. // Inorganic Chemistry. 2011. Vol. 50. No. 21. pp. 11263-11272.
GOST all authors (up to 50)
Copy
Nemykin V. V., Maskaev A. V., Geraskina M. R., S. Yusubov M., Zhdankin V. V. Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles. // Inorganic Chemistry. 2011. Vol. 50. No. 21. pp. 11263-11272.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ic201922n
UR - https://doi.org/10.1021/ic201922n
TI - Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles.
T2 - Inorganic Chemistry
AU - Nemykin, Victor V.
AU - Maskaev, Andrey V
AU - Geraskina, Margarita R
AU - S. Yusubov, Mekhman
AU - Zhdankin, Viktor V.
PY - 2011
DA - 2011/10/11
PB - American Chemical Society (ACS)
SP - 11263-11272
IS - 21
VL - 50
PMID - 21988373
SN - 0020-1669
SN - 1520-510X
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2011_Nemykin,
author = {Victor V. Nemykin and Andrey V Maskaev and Margarita R Geraskina and Mekhman S. Yusubov and Viktor V. Zhdankin},
title = {Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles.},
journal = {Inorganic Chemistry},
year = {2011},
volume = {50},
publisher = {American Chemical Society (ACS)},
month = {oct},
url = {https://doi.org/10.1021/ic201922n},
number = {21},
pages = {11263--11272},
doi = {10.1021/ic201922n}
}
Cite this
MLA
Copy
Nemykin, Victor V., et al. “Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles..” Inorganic Chemistry, vol. 50, no. 21, Oct. 2011, pp. 11263-11272. https://doi.org/10.1021/ic201922n.