Labeling of the neuropeptide enkephalin with functionalized tris(pyrazolyl)borate complexes: solid-phase synthesis and characterization of p-[Enk-OH]COC6H4TpPtMe3 and p-[Enk-OH]COC6H4TpMeRe(CO)3.

Bioconjugates of the neuropeptide Enkephalin (Enk = -Tyr-Gly-Gly-Phe-Leu-) labeled with organotransition metal tris-pyrazolylborate (Tp) complexes are reported. p-[Enk-OH]COC6H4TpPtMe3 and p-[Enk-OH]COC6H4Tp(Me)Re(CO)3 have been synthesized by solid-phase peptide synthesis (SPPS), purified by RP-HPLC, and characterized by ESI-mass spectrometry and 1H NMR and IR spectroscopies. p-[Enk-OH]COC6H4TpPtMe3 and p-[Enk-OH]COC6H4Tp(Me)Re(CO)3 constitute the first examples of Tp complexes employed in SPPS.

Synthesis and Structure of [Tp(Bu)()t()2]In, a Highly Twisted [Tris(3,5-di-tert-butylpyrazolyl)hydroborato]indium(I) Complex: Comparison with the Re-Evaluated Ordered Structure of [Tp(Bu)()t]In.

The indium(I) complex [Tp(Bu)()t()2]In ([Tp(Bu)()t()2] = tris(3,5-di-tert-butylpyrazolyl)hydroborato), synthesized by the reaction of [Tp(Bu)()t()2]Na with InCl, exhibits a structure in which the [Tp(Bu)()t()2] ligand adopts a highly twisted configuration due to steric interactions of the tert-butyl substituents in the 5-positions of the pyrazolyl groups. In contrast, the absence of 5-tert-butyl substituents allows the pyrazolyl groups in [Tp(Bu)()t]In to be coplanar with their respective In-N-N-B planes. The structure of [Tp(Bu)()t]In has been previously reported but was noted to exhibit an unusual type of disorder in which a nitrogen atom of one molecule was coincident with the boron atom of its disordered configuration [Dias, H.