The Silver–Alkene Interaction as a Supramolecular Synthon: Divinylbenzene-Based Assemblies
Jennifer Burgess A , Justine R. A. Cottam A and Peter J. Steel A BA Department of Chemistry, University of Canterbury, Christchurch 8020, New Zealand.
B Corresponding author. Email: peter.steel@canterbury.ac.nz
Australian Journal of Chemistry 59(5) 295-297 https://doi.org/10.1071/CH06147
Submitted: 2 May 2006 Accepted: 3 May 2006 Published: 13 June 2006
Abstract
The interaction of silver(i) salts with alkenes is shown to be a useful synthon for the assembly of both discrete and polymeric metallosupramolecular architectures. The three isomers of divinylbenzene lead to a diverse range of adducts, seven of which have been structurally characterized by X-ray crystallography.
Acknowledgment
We thank the Royal Society of New Zealand Marsden Fund for financial support.
[1]
(a) S. Leininger,
B. Olenyuk,
P. J. Stang,
Chem. Rev. 2000, 100, 853.
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and references therein.
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* 2: C20H20Ag2Cl2O8, monoclinic, P21/c, Z 4, wR 2 (all data) 0.1037, R 1 [I>2σ(I)] 0.0388. Crystallographic data have been deposited with the Cambridge Crystallographic Data Centre (CCDC; www.ccdc.cam.ac.uk/products/csd/request/) as deposition no. 603593).
† Despite several attempts, only a partial dataset was able to be collected for this unstable compound. However, this was sufficient to reveal the structure.
‡ 4: C30H30Ag2B2F8, monoclinic, P21/n, Z 8, wR 2 (all data) 0.1349, R 1 [I > 2σ(I)] 0.0543. CCDC 603594. Remarkably, this compound was also isolated as the sole product from the reaction of silver tetrafluoroborate with a commercial sample of a mixture of all three isomers of divinylbenzene.
¶ 5: C30H30Ag2Cl2O8, monoclinic, P21/n, Z 8, wR 2 (all data) 0.1229, R 1 [I > 2σ(I)] 0.0500. CCDC 603595.
‖‖ 6: C10H10AgClO4, monoclinic, P21/c, Z 4, wR 2 (all data) 0.0530, R 1 [I > 2σ(I)] 0.0213. CCDC 603596.
§ 7: C22H21Ag2F6O6.5S2, monoclinic, C2/c, Z 8, wR 2 (all data) 0.1145, R 1 [I > 2σ(I)] 0.0461. CCDC 603597.
** 8: C10H14Ag3Cl3O14, orthorhombic, Pnma, Z 4, wR 2 (all data) 0.1083, R 1 [I > 2σ(I)] 0.0364. CCDC 603598.