Home / Publications / Thermal polycondensation of hexakis(p-acetylphenoxy)-cyclotriphosphazene

Thermal polycondensation of hexakis(p-acetylphenoxy)-cyclotriphosphazene

7
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Chistyakov E. M. et al. Thermal polycondensation of hexakis(p-acetylphenoxy)-cyclotriphosphazene // Mendeleev Communications. 2018. Vol. 29. No. 1. pp. 99-101.
GOST all authors (up to 50) Copy
Chistyakov E. M., Buzin M. I., Aksenov S. M., Tupikov A. S., Kireev V. V. Thermal polycondensation of hexakis(p-acetylphenoxy)-cyclotriphosphazene // Mendeleev Communications. 2018. Vol. 29. No. 1. pp. 99-101.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2019.01.034
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.01.034
TI - Thermal polycondensation of hexakis(p-acetylphenoxy)-cyclotriphosphazene
T2 - Mendeleev Communications
AU - Chistyakov, Evgeniy Mikhailovich
AU - Buzin, Mikhail Igorevich
AU - Aksenov, Sergey Mikhailovich
AU - Tupikov, Anton Sergeyevich
AU - Kireev, Vyacheslav Vasil'evich
PY - 2018
DA - 2018/12/28
PB - Mendeleev Communications
SP - 99-101
IS - 1
VL - 29
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2018_Chistyakov,
author = {Evgeniy Mikhailovich Chistyakov and Mikhail Igorevich Buzin and Sergey Mikhailovich Aksenov and Anton Sergeyevich Tupikov and Vyacheslav Vasil'evich Kireev},
title = {Thermal polycondensation of hexakis(p-acetylphenoxy)-cyclotriphosphazene},
journal = {Mendeleev Communications},
year = {2018},
volume = {29},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.01.034},
number = {1},
pages = {99--101},
doi = {10.1016/j.mencom.2019.01.034}
}
MLA
Cite this
MLA Copy
Chistyakov, Evgeniy Mikhailovich, et al. “Thermal polycondensation of hexakis(p-acetylphenoxy)-cyclotriphosphazene.” Mendeleev Communications, vol. 29, no. 1, Dec. 2018, pp. 99-101. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.01.034.

Abstract

The thermal polycondensation of acetophenoxy groups in hexakis(p-acetylphenoxy)cyclotriphosphazene proceeds in two ways, namely, dimerization and trimerization, to produce chalcone or 1,3,5-triarylbenzene moieties, respectively. The polymers formed in both cases are thermally stable up to 400°C. The structure of hexakis(p-acetylphenoxy)cyclotriphosphazene has been established by X-ray study.

References

3.
Preparation of heat-moisture resistant epoxy resin based on phosphazene
Huang X., Wei W., Wei H., Li Y., Gu X., Tang X.
Journal of Applied Polymer Science, 2013
5.
Poly(organo)phosphazenes: recent progress in the synthesis and applications in tissue engineering and drug delivery
Khan R.U., Wang L., Yu H., Zain-ul-Abdin, Akram M., Wu J., Haroon M., Ullah R.S., Deng Z., Xia X.
Russian Chemical Reviews, 2018
6.
An initial study of hexavalent phosphazene salts as draw solutes in forward osmosis
9.
Polymeric dental composites modified with carboxy phosphazene methacrylates
Kireev V.V., Chistyakov E.M., Filatov S.N., Tupikov A.S., Panfilova D.V., Chetverikova A.I.
Russian Journal of Applied Chemistry, 2015
12.
Thermal polycondensation of hexa-p-hydroxymethylphenoxycyclotriphosphazene
Chistyakov E.M., Kireev V.V., Filatov S.N., Terekhov I.V., Buzin M.I., Komarova L.I.
Polymer Science - Series B, 2012
16.
10.1016/j.mencom.2019.01.034_bib0080
Petřiček
Jana 2006 Software Package, 2006
17.
Polyphenylenes and the related copolymer membranes for electrochemical device applications
19.
Ilgach D.M., Nosova G.I., Kopylova T.N., Nikonova E.N., Gadirov R.M., Smyslov R.Y., Litvinova L.S., Yakimansky A.V.
Mendeleev Communications, 2017