z-logo
Premium
Zinc Imine Polyhedral Oligomeric Silsesquioxane as a Quattro‐Site Catalyst for the Synthesis of Cyclic Carbonates from Epoxides and Low‐Pressure CO 2
Author(s) -
Janeta Mateusz,
Lis Tadeusz,
Szafert Sławomir
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202002996
Subject(s) - silsesquioxane , imine , chemistry , styrene , polymer chemistry , catalysis , homoleptic , nuclear magnetic resonance spectroscopy , thermogravimetric analysis , styrene oxide , inorganic chemistry , metal , organic chemistry , copolymer , polymer
In the present research, the synthesis, spectroscopic characterization, and structural investigations of a unique Zn II complex of imine‐functionalized polyhedral oligomeric silsesquioxane (POSS) is designed, and hereby described, as a catalyst for the synthesis of cyclic carbonates from epoxides and CO 2 . The uncommon features of the designed catalytic system is the elimination of the need for a high pressure of CO 2 and the significant shortening of reaction times commonly associated with such difficult transformations like that of styrene oxide to styrene carbonate. Our studies have shown that imine‐POSS is able to chelate metal ions like Zn II to form a unique coordination complex. The silsesquioxane core and the hindrance of the side arms (their steric effect) influence the construction process of the homoleptic Zn 4 @POSS‐1 complex. The compound was characterized in solution by NMR ( 1 H, 13 C, 29 Si), ESI‐MS, UV/Vis spectroscopy and in the solid state by thermogravimetric/differential thermal analysis (TG‐DTA), elemental analysis, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), cross‐polarization magic angle spinning (CP MAS) NMR ( 13 C, 29 Si) spectroscopy, and X‐ray crystallography.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here