A Family of Chiral Metal-Organic Frameworks

Gedrich K, Heitbaum M, Notzon A, Senkovska I, Frohlich R, Getzschmann J, Mueller U, Glorius F, Kaskel S

Research article (journal)

Abstract

Chiral metal organic frameworks with a three-dimensional network structure and wide-open pores (> 30 angstrom) were obtained by using chiral trifunctional linkers and multinuclear zinc clusters. The linkers, H(3)ChirBTB-n, consist of a 4,4',4 ''-benzene-1,3,5-triyltribenzoate (BTB) backbone decorated with chiral oxazolidinone substituents. The size and polarity of these substituents determines the network topology formed under solvothermal synthesis conditions. The resulting chiral MOFs adsorb even large molecules from solution. Moreover, they are highly active Lewis acid catalysts in the Mukaiyama aldol reaction. Due to their chiral functionalization, they show significant levels of enantioselectivity, thereby proving the validity of the modular design concept employed.

Details about the publication

JournalChemistry - A European Journal (Chem. Eur. J.)
Volume17
Issue7
Page range2099-2106
StatusPublished
Release year2011 (31/12/2011)
Language in which the publication is writtenEnglish
DOI10.1002/chem.201002568
Keywordsaldol reaction chirality dyes/pigments enantioselectivity metal-organic frameworks heterogeneous asymmetric hydrogenation pore-size catalytic-properties single-crystal hybrid solids ketones surface epoxidation adsorption polymers

Authors from the University of Münster

Fröhlich, Roland
Organic Chemistry Institute
Glorius, Frank
Professur für Organische Chemie (Prof. Glorius)