Journal
CRYSTAL GROWTH & DESIGN
Volume 10, Issue 8, Pages 3752-3756Publisher
AMER CHEMICAL SOC
DOI: 10.1021/cg1005874
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Funding
- R. A. Welch Foundation
- NHARP-Chemistry [003652-0092-2007]
- NSF [DMR-0706072]
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Four new divalent tin benzenedicarboxylates (bdc) have been synthesized by hydrothermal techniques, and their structures have been determined from single crystal X-ray data. A chiral complex layer is formed by Sn-II and 1,2-bdc. In Sn(1,2-bdc)-II (2), such layers are stacked in a AA pattern, leading to a chiral and polar structure with the space group symmetry C2, while in Sn(1,2-bdc)-I (1) the same layer is alternately stacked with the mirror-image layer, leading to a structure with the space group C2/c. The one-sided coordination of Sn-II combined with the 120 degrees angle of the carboxylate groups in 1,3-bdc results in the tubular structure of Sn(1,3-bdc) (3). The tubes are connected by very weak intertube Sn-O bonds. The compound Sn3O(1,4-bdc)(2) (4) has a 3D framework structure based on Sn3O triangular secondary building units that are cross-linked by the 1,4-bdc ligands. Strong pi-pi interactions occur between the neighboring phenyl rings.
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