Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution

The possibility to synthesize stereoregular tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane (tris-cis-tris-trans-[PhSi(O)OH]12) in an inorganic liquid medium – aqueous carbonic acid solution – was shown. The interaction of polyhedral phenylcoppersodiumsiloxane, {[(C6H5Si(O)O−]12(Cu...

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Published in:Green Chemistry Letters and Reviews
Main Authors: M. V. Shchemelinina, O. I. Shchegolikhina, Yu. A. Molodtsova, A. A. Anisimov, A. S. Goloveshkin, E. G. Kononova, M. A. Pigaleva, I. V. Elmanovich, M. O. Gallyamov, A. M. Muzafarov
Format: Article in Journal/Newspaper
Language:English
Published: Taylor & Francis Group 2016
Subjects:
Q
Online Access:https://doi.org/10.1080/17518253.2016.1151084
https://doaj.org/article/9d8fa7b2389f42d5a2fb3e112ad22e53
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spelling ftdoajarticles:oai:doaj.org/article:9d8fa7b2389f42d5a2fb3e112ad22e53 2023-05-15T15:52:00+02:00 Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution M. V. Shchemelinina O. I. Shchegolikhina Yu. A. Molodtsova A. A. Anisimov A. S. Goloveshkin E. G. Kononova M. A. Pigaleva I. V. Elmanovich M. O. Gallyamov A. M. Muzafarov 2016-01-01T00:00:00Z https://doi.org/10.1080/17518253.2016.1151084 https://doaj.org/article/9d8fa7b2389f42d5a2fb3e112ad22e53 EN eng Taylor & Francis Group http://dx.doi.org/10.1080/17518253.2016.1151084 https://doaj.org/toc/1751-8253 https://doaj.org/toc/1751-7192 1751-8253 1751-7192 doi:10.1080/17518253.2016.1151084 https://doaj.org/article/9d8fa7b2389f42d5a2fb3e112ad22e53 Green Chemistry Letters and Reviews, Vol 9, Iss 1, Pp 69-75 (2016) Polyhedral metallasiloxanes cyclic polysiloxanols carbonic acid Science Q Chemistry QD1-999 article 2016 ftdoajarticles https://doi.org/10.1080/17518253.2016.1151084 2022-12-31T12:21:06Z The possibility to synthesize stereoregular tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane (tris-cis-tris-trans-[PhSi(O)OH]12) in an inorganic liquid medium – aqueous carbonic acid solution – was shown. The interaction of polyhedral phenylcoppersodiumsiloxane, {[(C6H5Si(O)O−]12(Cu2+)4(Na+)4}*(L)m (L = Bun OH, H2O), with carbonic acid can be considered as a new ‘green’ method to obtain functional organosiloxane macrocycles. In contrast to the known methods, no organic solvents were used during the reaction. The identification of the structure of the end compound was performed by means of NMR and Infrared spectroscopy as well as X-ray crystallography. Article in Journal/Newspaper Carbonic acid Directory of Open Access Journals: DOAJ Articles Green Chemistry Letters and Reviews 9 1 69 75
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Polyhedral metallasiloxanes
cyclic polysiloxanols
carbonic acid
Science
Q
Chemistry
QD1-999
spellingShingle Polyhedral metallasiloxanes
cyclic polysiloxanols
carbonic acid
Science
Q
Chemistry
QD1-999
M. V. Shchemelinina
O. I. Shchegolikhina
Yu. A. Molodtsova
A. A. Anisimov
A. S. Goloveshkin
E. G. Kononova
M. A. Pigaleva
I. V. Elmanovich
M. O. Gallyamov
A. M. Muzafarov
Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution
topic_facet Polyhedral metallasiloxanes
cyclic polysiloxanols
carbonic acid
Science
Q
Chemistry
QD1-999
description The possibility to synthesize stereoregular tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane (tris-cis-tris-trans-[PhSi(O)OH]12) in an inorganic liquid medium – aqueous carbonic acid solution – was shown. The interaction of polyhedral phenylcoppersodiumsiloxane, {[(C6H5Si(O)O−]12(Cu2+)4(Na+)4}*(L)m (L = Bun OH, H2O), with carbonic acid can be considered as a new ‘green’ method to obtain functional organosiloxane macrocycles. In contrast to the known methods, no organic solvents were used during the reaction. The identification of the structure of the end compound was performed by means of NMR and Infrared spectroscopy as well as X-ray crystallography.
format Article in Journal/Newspaper
author M. V. Shchemelinina
O. I. Shchegolikhina
Yu. A. Molodtsova
A. A. Anisimov
A. S. Goloveshkin
E. G. Kononova
M. A. Pigaleva
I. V. Elmanovich
M. O. Gallyamov
A. M. Muzafarov
author_facet M. V. Shchemelinina
O. I. Shchegolikhina
Yu. A. Molodtsova
A. A. Anisimov
A. S. Goloveshkin
E. G. Kononova
M. A. Pigaleva
I. V. Elmanovich
M. O. Gallyamov
A. M. Muzafarov
author_sort M. V. Shchemelinina
title Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution
title_short Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution
title_full Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution
title_fullStr Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution
title_full_unstemmed Synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution
title_sort synthesis of macrocyclic tris-cis-tris-trans- dodeca[(phenyl)(hydroxy)]cyclododecasiloxane in carbonic acid solution
publisher Taylor & Francis Group
publishDate 2016
url https://doi.org/10.1080/17518253.2016.1151084
https://doaj.org/article/9d8fa7b2389f42d5a2fb3e112ad22e53
genre Carbonic acid
genre_facet Carbonic acid
op_source Green Chemistry Letters and Reviews, Vol 9, Iss 1, Pp 69-75 (2016)
op_relation http://dx.doi.org/10.1080/17518253.2016.1151084
https://doaj.org/toc/1751-8253
https://doaj.org/toc/1751-7192
1751-8253
1751-7192
doi:10.1080/17518253.2016.1151084
https://doaj.org/article/9d8fa7b2389f42d5a2fb3e112ad22e53
op_doi https://doi.org/10.1080/17518253.2016.1151084
container_title Green Chemistry Letters and Reviews
container_volume 9
container_issue 1
container_start_page 69
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