Endocarditis associated with contamination of cardiovascular bioprostheses with Mycobacterium chelonae: a collaborative microbiological study.

Background: Mycobacterium chelonae is a rare cause of infective endocarditis that is difficult to diagnose and treat. After we found M chelonae in a series of patients, we aimed to investigate its role in cardiovascular prosthesis dysfunction and contamination of bioprostheses as a possible cause of infection.

Methods: In this collaborative microbiological study, we report on nine patients treated in three cardiovascular surgical departments in Germany, who were found to have M chelonae infection after receiving BioIntegral bioprostheses.

New porphyrinoids: vanadyl(IV) complexes of meso-aryl-substituted corrphycene and 10-oxocorrole ligands.

Rare vanadyl corrphycene and vanadyl 10-oxocorrole complexes were obtained via an oxidative macrocyclization process by the treatment of 6,6'-di-p-tolyl-2,2'-bidipyrrin with VO(acac)2 in a hot dioxygen atmosphere. The geometric and electronic structures of the new porpyhrinoids were determined and showed the dependency of the spectral pattern from the aromaticity of the macrocyclic ligand.

Free-base tripyrrins.

The hitherto unavailable free-base tripyrrins HTrpy have been prepared by cyanide promoted demetallation of a nickel(ii) tripyrrin and by acid-induced condensation of a diformylpyrrole and an alkylpyrrole with a sterically shielded alpha-position.

Cyanide-promoted demetalation of TrpyNiNCO: a route to sensitive metallotripyrrins of CoII, FeII, and MnII.

Etheral solutions of free base tripyrrins (HTrpy) were prepared by treatment of nickel isocyanate complexes (TrpyNiNCO) with excess cyanide. From these solutions sensitive metallotripyrrins with cobalt(II), iron(II), and manganese(II) ions (TrpyMX) and with a choice of external ligands X could be obtained in pure, crystalline form. Four cobalt and one iron chelate were characterized by X-ray crystallography.

Monomeric and polymeric copper and zinc tripyrrins.

Neutral transition metal complexes of different alpha,omega-dimethyltripyrrins TrpyMX with M = Cu(II) and Zn(II) have been prepared with a variety of anionic halogeno and pseudohalogeno ligands X, and have been studied with respect to coordination modes and structural distortion. Only four- and five-coordinate species have been observed throughout the series. All four-coordinate species display unstrained, but distorted tetrahedral or strained and distorted square-planar coordination environments for zinc(II) and copper(II) species, respectively, thus following the expectations from simple ligand field arguments.

Pillars, layers, pores and networks from nickeltripyrrins: a porphyrin fragment as a versatile building block for the construction of supramolecular assemblies.

Sterically hindered nickel- tripyrrins [Ni(trpy)X] with different di-, tri- and tetradentate anions X have been prepared with the aim of finding coordination polymers formed by self-association. The syntheses were performed by simple ligand-exchange reactions and proceeded successfully with the pseudohalides CN(-), OCN(-), SCN(-), SeCN(-), N(CN)(2) (-) (dicyanoamido, dca) and C(CN)(3) (-) (tricyanomethanido, tcm), the cyanidometallates [Ag(CN)(2)](-) and [Ni(CN)(4)](2-) and the salicylate anion (sal(-)). X-ray crystallographic analyses revealed that the complexes with cyanido and isocyanato ligands, as well as the compound with a salicylato ligand, are prototypes for structurally distinct monomeric species in the solid state, whereas one-dimensional coordination polymers or supramolecular three-dimensional networks are formed from all other combinations.

Unexpected formation and structural characterisation of a novel rhodium B12 analogue.

The metalation reactions of the 2,2'-bidipyrrin 4 with different rhodium(I) precursors yield the complexes 5 and 6 and the unusual corrinoid 7, depending only on the type of the ancillary ligand employed.