2,4,6-Triarylphosphinines versus 2,4,6-Triarylpyridines: An Investigation of the Differences in Reactivity between Structurally Related Aromatic Phosphorus and Nitrogen Heterocycles

• Published in: Chemistry : a European journal Vol. 19; no. 43; pp. 14458 - 14469
• Main Authors: Weemers, Jarno J. M., Wiecko, Jelena, Pidko, Evgeny A., Weber, Manuela, Lutz, Martin, Müller, Christian
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag 18-10-2013; WILEY‐VCH Verlag; Wiley Subscription Services, Inc
• Subjects: Activation; Analogue; Chemistry; coordination chemistry; Crystal structure; Dehydrogenation; Derivatives; heterocycles; Joining; Mathematical analysis; phosphinines; Phosphorus; Pyridines; phosphinines; pyridines; heterocycles; coordination chemistry
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/chem.201302441

The novel atropisomeric pyridine derivative rac‐10 has been synthesized and structurally characterized. In contrast to its phosphorus analogue 3, axially chiral 10 has a considerably lower rotational barrier as estimated by DFT calculations. However, the presence of the two enantiomers could be confirmed by means of chiral analytical HPLC analysis and by protonation experiments with a chiral acid. Compound rac‐10 could be further dehydrogenated by treatment with DDQ to the benzo(h)quinoline derivative rac‐12. This conversion failed for the phosphorus analogue rac‐3. Interestingly, although 2,4,6‐triarylphosphinines undergo facile CH activation with [Cp*IrCl2]2 in the presence of NaOAc, this reaction does not proceed with the corresponding pyridine derivatives. On the other hand, the latter ones can be selectively ortho‐metalated with Pd(OAc)2, leading to acetate‐bridged dimeric species, which could be unambiguously confirmed by means of X‐ray crystal structure analysis. The treatment of phosphinines with Pd(OAc)2 led instead to the formation of the unusual cofacial oxidative coupling products 16 and 17, which consist of a phosphorus‐containing cage structure.
The right balance: Although phosphinines undergo facile CH activation with [Cp*IrCl2]2 in the presence of NaOAc, this reaction does not proceed with the corresponding pyridine derivatives. The latter can be selectively ortho‐metalated with Pd(OAc)2, leading to acetate‐bridged dimeric species. The treatment of phosphinines with Pd(OAc)2 led to unusual cofacial oxidative coupling products.