Research Article: Racemic tricarbon­yl[7-meth­oxy-2-(η6-phen­yl)chromane]­chromium(0)

Date Published: April 01, 2011

Publisher: International Union of Crystallography

Author(s): Mukut Gohain, Theunis J. Muller, Barend C. B. Bezuidenhoudt.

http://doi.org/10.1107/S1600536811008683

Abstract

In the title compound, [Cr(C16H16O2)(CO)3], the Cr0 atom of the Cr(CO)3 unit is coordinated to the phenyl ring of the flavan ligand in an η6 mode, with a normal arene-to-metal distance. The Cr(CO)3 unit exhibits a three-legged piano-stool conformation, while the dihydro­pyran ring displays a distorted envelope configuration. The phenyl ring is twisted away from the fused ring system by 25.5 (2)°. The meth­oxy group is almost coplanar with the phenyl ring [CMe—O—Car—Car torsion angle = 8.46 (2)°]. The crystal packing is stabilized by inter­molecular C—H⋯O inter­actions.

Partial Text

For similar structures, see: van Tonder et al. (2010a ▶,b ▶) and for other related structures, see: van Tonder et al. (2009a ▶,b ▶). For the synthesis of the title compound, see: Müller et al. (1999 ▶) and for the sythesis of 7-meth­oxy­flavan-4-one, see: Sato et al. (2006 ▶). For standard bond lengths, see: Allen et al. (1987 ▶). For the importance of flavonoids in biological investigations, see: Rice-Evans & Packer (2003 ▶). For the use of tricarbon­yl(arene)chromium complexes in regioselective organic synthesis, see: Muschalek et al. (2007 ▶).

 

Source:

http://doi.org/10.1107/S1600536811008683

 

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