Oligonucleotides Incorporating Palladacyclic Nucleobase Surrogates.

An oligonucleotide incorporating a palladacyclic nucleobase has been prepared by ligand-directed metalation of a phenylpyridine moiety. This oligonucleotide hybridized with natural counterparts placing any of the canonical nucleobases opposite to the palladacyclic residue. The palladated duplexes had B-type conformation and melting temperatures comparable to those of respective unmodified duplexes with a single mismatch. In the duplexes placing C, G or T (but not A) opposite to the palladacyclic residue, greatly increased absorptivity suggested formation of a Pd -mediated base pair. Absorptivity and ellipticity of these duplexes persisted even at the highest temperatures applicable in T and CD experiments (90 °C). Evidently the Pd -mediated base pairs do not dissociate under the experimental conditions.