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Published in

International Union of Crystallography, Acta Crystallographica Section E: Structure Reports Online, 11(63), p. o4390-o4391, 2007

DOI: 10.1107/s1600536807051136

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2,3,5′,6,6′,7-Hexamethoxy-3′ H ,10 H -spiro[anthracene-9,1′-isobenzofuran]-3′,10-dione

Journal article published in 2007 by Marlon R. Lutz, Matthias Zeller ORCID, Daniel P. Becker
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

The title molecule, C27H24O9, was formed via a transannular electrophilic addition of a putative cyclotriveratrylene triketone and is made up of an anthrone and an isobenzofuranone ring that are connected via one C atom to form a spiro compound. The anthracene and isobenzofuranone ring systems of the spiro compound are both essentially planar and perpendicular to each other, with an angle of 89.90 (2)° between them. The rigid molecule crystallizes with large voids of 598.7 Å3, or 21.5% of the unit-cell volume, that are partially filled with unmodelled disordered solvent molecules. The voids stretch as infinite channels along the [101] direction. The packing of the structure is partially stabilized by a range of weak C—H...O hydrogen bonds and also by C—H...π interactions. No significant π–π interactions are present in the crystal structure.