Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

The Silver–Alkene Interaction as a Supramolecular Synthon: Divinylbenzene-Based Assemblies

Jennifer Burgess A , Justine R. A. Cottam A and Peter J. Steel A B
+ Author Affiliations
- Author Affiliations

A 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.


References


[1]   (a) S. Leininger, B. Olenyuk, P. J. Stang, Chem. Rev. 2000, 100,  853.
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |   and references therein.
        | Crossref |  GoogleScholarGoogle Scholar |  open url image1




* 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.