volume 50 issue 21 pages 11263-11272

Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles.

Publication typeJournal Article
Publication date2011-10-11
scimago Q1
wos Q1
SJR0.958
CiteScore7.4
Impact factor4.7
ISSN00201669, 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.
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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.
RIS |
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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 -
BibTex |
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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}
}
MLA
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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.