volume 43 issue 12 pages 843-851

New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group

Publication typeJournal Article
Publication date2017-12-07
scimago Q4
wos Q4
SJR0.189
CiteScore1.7
Impact factor1.1
ISSN10703284, 16083318
General Chemistry
General Chemical Engineering
Abstract
The following new triphenylantimony(V) catecholate complexes bearing the protonated imine group are synthesized from the new sterically hindered 3,5-di-tert-butylpyrocatechols (6-(CH=N-o-(C6H4–NH2))-3,5-Cat)H2 (H2L1) and (6-(CH=N-o-(C6H4–OH))-3,5-Cat)H2 (H2L2) containing in position 6 the iminomethyl group bonded to the aniline or phenol substituent: (6-(CH=NH+-o-(C6H4–NH2))-3,5-Cat)SbPh3X (X = Br (I), OMe (III)) and (6-(CH=NH+-o-(C6H4–OH))-3,5-Cat)SbPh3X (X = Br (II), OMe (IV)). The molecular structure of complex III · CH 3 OH in the crystalline state is determined by X-ray diffraction analysis (CIF file CCDC no. 1554694). The electrochemical properties of complexes III and IV are studied by cyclic voltammetry.
Found 
Found 

Top-30

Journals

1
2
3
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
3 publications, 30%
Dalton Transactions
2 publications, 20%
Molecules
1 publication, 10%
Journal of Organometallic Chemistry
1 publication, 10%
ACS Omega
1 publication, 10%
Journal of the American Chemical Society
1 publication, 10%
1
2
3

Publishers

1
2
3
Pleiades Publishing
3 publications, 30%
Elsevier
2 publications, 20%
American Chemical Society (ACS)
2 publications, 20%
Royal Society of Chemistry (RSC)
2 publications, 20%
MDPI
1 publication, 10%
1
2
3
  • 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
10
Share
Cite this
GOST |
Cite this
GOST Copy
Poddelsky A. I. et al. New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group // Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2017. Vol. 43. No. 12. pp. 843-851.
GOST all authors (up to 50) Copy
Poddelsky A. I., Arsenev M. V., Okhlopkova L. S., Smolyaninov I. V., Fukin G. K. New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group // Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2017. Vol. 43. No. 12. pp. 843-851.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1134/S1070328417120089
UR - https://doi.org/10.1134/S1070328417120089
TI - New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group
T2 - Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
AU - Poddelsky, A I
AU - Arsenev, M V
AU - Okhlopkova, L S
AU - Smolyaninov, I V
AU - Fukin, G. K.
PY - 2017
DA - 2017/12/07
PB - Pleiades Publishing
SP - 843-851
IS - 12
VL - 43
SN - 1070-3284
SN - 1608-3318
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2017_Poddelsky,
author = {A I Poddelsky and M V Arsenev and L S Okhlopkova and I V Smolyaninov and G. K. Fukin},
title = {New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group},
journal = {Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya},
year = {2017},
volume = {43},
publisher = {Pleiades Publishing},
month = {dec},
url = {https://doi.org/10.1134/S1070328417120089},
number = {12},
pages = {843--851},
doi = {10.1134/S1070328417120089}
}
MLA
Cite this
MLA Copy
Poddelsky, A. I., et al. “New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group.” Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, vol. 43, no. 12, Dec. 2017, pp. 843-851. https://doi.org/10.1134/S1070328417120089.