Home / Publications / Synthesis of New Heteroatomic Podands from Ethyl 2-[(2-Aminophenylamino)Methylidene]-3-Oxoalkanoates and Thiophene-2,5-Dicarboxaldehyde

Synthesis of New Heteroatomic Podands from Ethyl 2-[(2-Aminophenylamino)Methylidene]-3-Oxoalkanoates and Thiophene-2,5-Dicarboxaldehyde

Yulia Sergeevna Kudyakova 1
Yulia Sergeevna Kudyakova
, 
Yanina Valer'evna Burgart 1
Yanina Valer'evna Burgart
, 
Pavel Alexandrovich Slepukhin 1
Pavel Alexandrovich Slepukhin
, 
Viktor Ivanovich Saloutin 1
Viktor Ivanovich Saloutin
10.1016/j.mencom.2012.09.020
Published 2012-09-17
Communication , Volume 22, Issue 5, 284-286
6
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Kudyakova Y. S. et al. Synthesis of New Heteroatomic Podands from Ethyl 2-[(2-Aminophenylamino)Methylidene]-3-Oxoalkanoates and Thiophene-2,5-Dicarboxaldehyde // Mendeleev Communications. 2012. Vol. 22. No. 5. pp. 284-286.
GOST all authors (up to 50) Copy
Kudyakova Y. S., Burgart Y. V., Slepukhin P. A., Saloutin V. I. Synthesis of New Heteroatomic Podands from Ethyl 2-[(2-Aminophenylamino)Methylidene]-3-Oxoalkanoates and Thiophene-2,5-Dicarboxaldehyde // Mendeleev Communications. 2012. Vol. 22. No. 5. pp. 284-286.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2012.09.020
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.09.020
TI - Synthesis of New Heteroatomic Podands from Ethyl 2-[(2-Aminophenylamino)Methylidene]-3-Oxoalkanoates and Thiophene-2,5-Dicarboxaldehyde
T2 - Mendeleev Communications
AU - Kudyakova, Yulia Sergeevna
AU - Burgart, Yanina Valer'evna
AU - Slepukhin, Pavel Alexandrovich
AU - Saloutin, Viktor Ivanovich
PY - 2012
DA - 2012/09/17
PB - Mendeleev Communications
SP - 284-286
IS - 5
VL - 22
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2012_Kudyakova,
author = {Yulia Sergeevna Kudyakova and Yanina Valer'evna Burgart and Pavel Alexandrovich Slepukhin and Viktor Ivanovich Saloutin},
title = {Synthesis of New Heteroatomic Podands from Ethyl 2-[(2-Aminophenylamino)Methylidene]-3-Oxoalkanoates and Thiophene-2,5-Dicarboxaldehyde},
journal = {Mendeleev Communications},
year = {2012},
volume = {22},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.09.020},
number = {5},
pages = {284--286},
doi = {10.1016/j.mencom.2012.09.020}
}
MLA
Cite this
MLA Copy
Kudyakova, Yulia Sergeevna, et al. “Synthesis of New Heteroatomic Podands from Ethyl 2-[(2-Aminophenylamino)Methylidene]-3-Oxoalkanoates and Thiophene-2,5-Dicarboxaldehyde.” Mendeleev Communications, vol. 22, no. 5, Sep. 2012, pp. 284-286. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.09.020.

Abstract

Condensation of two moles of ethyl 2-[(2-aminophenylamino)methylidene]-3-oxo-3-(polyfluoroalkyl)propionates with 2,5-thiophene-dicarboxaldehyde results in new heteroatomic podands. X-ray data showed that in the solid state these molecules arrange in two independent chelating fragments of b-amino enone type, thiophene fragment being a spacer.

References

1.
10.1016/j.mencom.2012.09.020_bib0005
Izatt
Synthesis of Macrocycle: The Design of Selective Complexing Agents, 1987
2.
10.1016/j.mencom.2012.09.020_bib0010
Lindoy
The Chemistry of Macrocyclic Ligand Complexes, 1989
4.
Magnetic clusters: Spinning into control
Sessoli R.
Nature Chemistry, 2010
5.
An Unprecedented Charge Transfer Induced Spin Transition in an Fe-Os Cluster
Hilfiger M., Chen M., Brinzari T., Nocera T., Shatruk M., Petasis D., Musfeldt J., Achim C., Dunbar K.
Angewandte Chemie - International Edition, 2010
7.
Material Applications for Salen Frameworks
Wezenberg S., Kleij A.
Angewandte Chemie - International Edition, 2008
9.
Salen Ligands Revisited: Synthesis and Application of a Planar Chiral “Ferro‐Salen” Ligand
Niemeyer J., Kehr G., Fröhlich R., Erker G.
European Journal of Inorganic Chemistry, 2010
12.
New enamine ligands derived from ethyl 2-ethoxymethylidene-3-oxo-3-polyfluoroalkylpropionates and o-phenylenediamine
Kudyakova Y.S., Goryaeva M.V., Burgart Y.V., Slepukhin P.A., Saloutin V.I.
Russian Chemical Bulletin, 2010
13.
Yu. S. Kudyakova, Ya. V. Burgart and V. I. Saloutin, Khim. Geterotsikl. Soedin., 2011, 677.[Chem. Heterocycl. Compd. (Engl. Transl.), 2011, 47, 558].
14.
Dinucleating macrocyclic Schiff bases derived from thiophene and their metal complexes: the crystal structures of a free macrocycle and of a disilver complex
Bailey N.A., Eddy M.M., Fenton D.E., Moss S., Mukhopadhyay A., Jones G.
Journal of the Chemical Society Dalton Transactions, 1984
15.
Guerriero P., Vigato P.A., Fenton D.E., Hellier P.C., Abildgaard F., Led J.J., Christensen S.B.
Acta Chemica Scandinavica, 2008
16.
The challenge of cyclic and acyclic schiff bases and related derivatives
Vigato P.A., Tamburini S.
Coordination Chemistry Reviews, 2004
18.
The disorder of perfluoroalkyl chains in crystals: Two case histories of interpretation and refinement
Dey A., Metrangolo P., Pilati T., Resnati G., Terraneo G., Wlassics I.
Journal of Fluorine Chemistry, 2009
19.
A short history of SHELX
Sheldrick G.M.
Acta Crystallographica Section A Foundations of Crystallography, 2007