Home / Publications / Dimethyl sulfoxide as a green solvent for successful precipitative polyheterocyclization based on nucleophilic aromatic substitution, resulting in high molecular weight PIM-1

Dimethyl sulfoxide as a green solvent for successful precipitative polyheterocyclization based on nucleophilic aromatic substitution, resulting in high molecular weight PIM-1

Igor Igorevich Ponomarev 1
Igor Igorevich Ponomarev
Inesa Vasil'evna Blagodatskikh
Alexander Vasil'evich Muranov 1
Alexander Vasil'evich Muranov
Yulia Aleksandrovna Volkova 1
Yulia Aleksandrovna Volkova
Ivan Igorevich Ponomarev 1
Ivan Igorevich Ponomarev
Published 2016-07-07
CommunicationVolume 26, Issue 4, 362-364
31
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Ponomarev I. I. et al. Dimethyl sulfoxide as a green solvent for successful precipitative polyheterocyclization based on nucleophilic aromatic substitution, resulting in high molecular weight PIM-1 // Mendeleev Communications. 2016. Vol. 26. No. 4. pp. 362-364.
GOST all authors (up to 50) Copy
Ponomarev I. I., Blagodatskikh I. V., Muranov A. V., Volkova Y. A., Razorenov D. Y., Ponomarev I. I., Skupov K. M. Dimethyl sulfoxide as a green solvent for successful precipitative polyheterocyclization based on nucleophilic aromatic substitution, resulting in high molecular weight PIM-1 // Mendeleev Communications. 2016. Vol. 26. No. 4. pp. 362-364.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2016.07.033
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.07.033
TI - Dimethyl sulfoxide as a green solvent for successful precipitative polyheterocyclization based on nucleophilic aromatic substitution, resulting in high molecular weight PIM-1
T2 - Mendeleev Communications
AU - Ponomarev, Igor Igorevich
AU - Blagodatskikh, Inesa Vasil'evna
AU - Muranov, Alexander Vasil'evich
AU - Volkova, Yulia Aleksandrovna
AU - Razorenov, Dmitriy Yur'evitch
AU - Ponomarev, Ivan Igorevich
AU - Skupov, Kirill Mikhailovich
PY - 2016
DA - 2016/07/07
PB - Mendeleev Communications
SP - 362-364
IS - 4
VL - 26
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2016_Ponomarev,
author = {Igor Igorevich Ponomarev and Inesa Vasil'evna Blagodatskikh and Alexander Vasil'evich Muranov and Yulia Aleksandrovna Volkova and Dmitriy Yur'evitch Razorenov and Ivan Igorevich Ponomarev and Kirill Mikhailovich Skupov},
title = {Dimethyl sulfoxide as a green solvent for successful precipitative polyheterocyclization based on nucleophilic aromatic substitution, resulting in high molecular weight PIM-1},
journal = {Mendeleev Communications},
year = {2016},
volume = {26},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.07.033},
number = {4},
pages = {362--364},
doi = {10.1016/j.mencom.2016.07.033}
}
MLA
Cite this
MLA Copy
Ponomarev, Igor Igorevich, et al. “Dimethyl sulfoxide as a green solvent for successful precipitative polyheterocyclization based on nucleophilic aromatic substitution, resulting in high molecular weight PIM-1.” Mendeleev Communications, vol. 26, no. 4, Jul. 2016, pp. 362-364. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.07.033.

Abstract

A new method for the effective synthesis of high molecular weight polymer of intrinsic microporosity (PIM-1) powder widely employed for gas separation membranes was successfully developed using precipitative polyheterocyclization process in non-toxic DMSO.

References

1.
Solution‐Processed, Organophilic Membrane Derived from a Polymer of Intrinsic Microporosity
Budd P. ., Elabas E. ., Ghanem B. ., Makhseed S., McKeown N. ., Msayib K. ., Tattershall C. ., Wang D.
Advanced Materials, 2004
3.
Polymers of intrinsic microporosity (PIMs): robust, solution-processable, organic nanoporous materials
Budd P.M., Ghanem B.S., Makhseed S., McKeown N.B., Msayib K.J., Tattershall C.E.
Chemical Communications, 2004
4.
Kurmaz S.V., Grubenko G.A., Knerelman E.I., Davydova G.I., Torbov V.I., Dremova N.N.
Mendeleev Communications, 2014
5.
Polymeric Gas Separation Membranes
Yampolskii Y.
Macromolecules, 2012
6.
Yaroslavtsev A.B., Yampolskii Y.P.
Mendeleev Communications, 2014
9.
Perspective on Solvent Use in the Pharmaceutical Industry
Constable D.J., Jimenez-Gonzalez C., Henderson R.K.
Organic Process Research and Development, 2006
10.
10.1016/j.mencom.2016.07.033_bib0035
Ponomarev
1991
11.
10.1016/j.mencom.2016.07.033_bib0040
Ponomarev
Vysokomol. Soedin. A, 1992
12.
Intramolecular Reaction in Polycondensations. I. The Theory of Linear Systems
Jacobson H., Stockmayer W.H.
Journal of Chemical Physics, 1950
13.
10.1016/j.mencom.2016.07.033_bib0050
Flory
Principles of Polymer Chemistry, 1953
14.
10.1016/j.mencom.2016.07.033_bib0055
Blagodatskikh
e-Polymers, 2005
15.
Cyclic and telechelic ladder polymers derived from tetrahydroxytetramethylspirobisindane and 1,4-dicyanotetrafluorobenzene
Kricheldorf H.R., Lomadze N., Fritsch D., Schwarz G.
Journal of Polymer Science, Part A: Polymer Chemistry, 2006