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

• 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: Text
• Language: unknown
• Published: Taylor & Francis 2016
• Subjects: Biophysics; Biochemistry; Medicine; 39999 Chemical Sciences not elsewhere classified; FOS Chemical sciences; Carbonic acid
• Online Access: https://dx.doi.org/10.6084/m9.figshare.3115501.v1; https://figshare.com/articles/Synthesis_of_macrocyclic_tris_i_cis_i_tris_i_trans_i_dodeca_phenyl_hydroxy_cyclododecasiloxane_in_carbonic_acid_solution/3115501/1

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, {[(C 6 H 5 Si(O)O − ] 12 (Cu 2 + ) 4 (Na + ) 4 }*(L) m (L = Bu n OH, H 2 O), 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.