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Sammanfattning

The first representatives of alkoxy-zircono-silsesquioxane compounds, dinuclear [Cy(7)Si(7)O(12)]Zr(ROH)(mu-OR)(2)Zr(ROH)[O(12)Si(7)Cy(7)], where R = (n)Pr, (n)Bu, (t)Bu: Cy = c-C(6)H(11), and [Cy*(7)Si(7)O(12)]Zr(mu-ROH)(mu-OR)(2)Zr [O(12)Si(7)Cy*(7)], R = (t)Bu; Cy* = c-C(5)H(9), have been prepared with quantitative yield by interaction of the corresponding zirconium alkoxides with the cycloalkyl-substituted cage silsesquioxanes in hexane. The Xray single crystal study of the n-butoxide derivative revealed that zirconium atoms are hexacoordinated with the 3 oxygen atoms of the cage ligand, 2 from the bridging alkoxide groups and one from the solvating alcohol molecule in the coordination sphere. The molecule is additionally supported by a hydrogen bond between the solvating alcohol and an oxygen atom belonging to the cage ligand coordinated by the other zirconium atom. The structures of produced silsesquioxanes display behavior typical for metal-organic frameworks as they crystallize initially as hexane clathrates, but lose the solvent on storage in inert atmosphere. This results in formation of empty channels situated along the c-axis. (C) 2010 Elsevier B.V. All rights reserved.

Nyckelord

Metalla-silsesquioxanes; Zr-POSS; X-ray structure; Molecular model; Epoxidation catalyst; Hybrid material; MOF

Publicerad i

Inorganic Chemistry Communications
2010, volym: 13, nummer: 6, sidor: 774-777
Utgivare: ELSEVIER SCIENCE BV

SLU författare

UKÄ forskningsämne

Livsmedelsvetenskap

Publikationens identifierare

  • DOI: https://doi.org/10.1016/j.inoche.2010.03.044

Permanent länk till denna sida (URI)

https://res.slu.se/id/publ/48143