Synthesis and studies of benzoxazinesiloxanes
- Authors: Sokolik V.N.1, Gizatullin S.F.1, Raigorodskii I.M.1, Kopylov V.M.1, Salikhov T.R.2
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Affiliations:
- M. V. Lomonosov Moscow State University of Fine Chemical Technologies
- All-Russian Scientific Research Institute of Aviation Materials
- Issue: Vol 65, No 4 (2016)
- Pages: 1027-1033
- Section: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/237823
- DOI: https://doi.org/10.1007/s11172-016-1408-x
- ID: 237823
Cite item
Abstract
A synthesis of organosilicon 1,3-benzoxazines (BZ-Si) was accomplished by the reaction of organic phenols, paraformaldehyde and 3-aminopropyl(trialkoxy)silanes, as well as organosilicon phenols of the general formula R´[SiMe2O]n[SiMeRO]mSiMe2R´ (R´ is 4-hydroxy-3methoxyphenylpropyl-, R is methylor 4-hydroxy-3-methoxyphenylpropyl), paraformaldehyde, and aniline (or monoethanolamine). The structure of BZ-Si was confirmed by NMR and IR spectroscopy. The studies of BZ-Si by DSC showed that the benzoxazine ring opening takes place in the temperature range 130—265 °C. The temperature of 5% mass loss of BZ-Si in air is within 220—270 °C (TGA).
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About the authors
V. N. Sokolik
M. V. Lomonosov Moscow State University of Fine Chemical Technologies
Author for correspondence.
Email: sokolikv@mail.ru
Russian Federation, 86 prosp. Vernadskogo, Moscow, 119571
Sh. F. Gizatullin
M. V. Lomonosov Moscow State University of Fine Chemical Technologies
Email: sokolikv@mail.ru
Russian Federation, 86 prosp. Vernadskogo, Moscow, 119571
I. M. Raigorodskii
M. V. Lomonosov Moscow State University of Fine Chemical Technologies
Email: sokolikv@mail.ru
Russian Federation, 86 prosp. Vernadskogo, Moscow, 119571
V. M. Kopylov
M. V. Lomonosov Moscow State University of Fine Chemical Technologies
Email: sokolikv@mail.ru
Russian Federation, 86 prosp. Vernadskogo, Moscow, 119571
T. R. Salikhov
All-Russian Scientific Research Institute of Aviation Materials
Email: sokolikv@mail.ru
Russian Federation, 17 ul. Radio, Moscow, 105005
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