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- Publisher
- Wiley
- Copyright
- Copyright © 2011 Wiley Periodicals, Inc.
- ISSN
- 1042-7163
- eISSN
- 1098-1071
- DOI
- 10.1002/hc.20747
- Publisher site
- See Article on Publisher Site
Abstract
A number of different complexation structures of cis‐1,4‐dihydro‐1,4‐dimethyl‐2,3,5,6‐tetrakis(t‐butoxycarbonyl)‐1,4‐diarsinine (cis‐DHDAtBu) with gold(I) and iridium(III) were synthesized and characterized by 1H, 13C NMR spectra, X‐ray crystallography, and elemental analysis. Mono‐ and di‐nuclear gold(I) chloride complexes with cis‐DHDAtBu were obtained by simple addition of gold(I) chloride to cis‐DHDAtBu. A hetero‐trinuclear gold‐platinum‐gold complex (PtAu2Cl4(cis‐DHDAtBu)2) was obtained by complexation of a mononuclear platinum(II) complex (trans‐PtCl2(cis‐DHDAtBu)2), which was obtained by complexation of cis‐DHDAtBu with a half‐equimolar amount of PtCl2(PhCN)2, with a twice‐equimolar amount of gold(I) chloride. An iridium(III) complex with cis‐DHDAtBu (IrCl3(cis‐DHDAtBu)2) was prepared from hydrated iridium(III) chloride and cis‐DHDAtBu. The complex comprises a five‐membered chelate cis‐DHDAtBu and an usual monodentate cis‐DHDAtBu. The interior angles at around the arsenic and the As–C—C bond angles were significantly varied from 113.4° to 129.4° in the present crystal. These observations suggest that the flexibility of the bond angles at around the arsenic center is inherent property in the present organoarsenic compounds. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 23:16–26, 2012; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.20747
Journal
Heteroatom Chemistry – Wiley
Published: Jan 1, 2012