Multimodality imaging in the diagnosis of bioprosthetic aortic valve endocarditis: A case report.

Introduction: Prosthetic valve infective endocarditis (PVE) is a diagnostic challenge even in the era of multimodality cardiovascular imaging. Case presentation: The patient was a 67-year-old male with a three-year history of bioprosthetic aortic valve replacement who presented with persistent fever and negative blood cultures. The initial transthoracic echocardiography revealed a thickened aortic root. An abscess formation was visualized upon subsequent three-dimensional transesophageal echocardiography and positron emission tomography/computerized tomography (PET/CT). The patient underwent an urgent necrotic tissue debridement and a redo Bentall surgery. The real-time polymerase chain reaction of excised tissues was positive for Streptococcus. Clinical discussion: The diagnosis of PVE and its complications requires the integration of clinical, microbiological, and serial imaging data. Although advanced imaging modalities like PET/CT allow a timely diagnosis and management, their routine use in resource-limited scenarios is difficult. Conclusion: Multimodality cardiovascular imaging plays an important role in the diagnosis of PVE. Serial echocardiographic and clinical assessments are possible alternatives when the access to advanced cardiovascular imaging modalities is limited.

Correction: Homo-condensation of acetophenones toward imidazothiones.

[This corrects the article DOI: 10.1039/D0RA03047C.].

Homo-condensation of acetophenones toward imidazothiones.

Direct synthesis of imidazothiones from simple, commercial substrates is not known. We report a method for the condensation of acetophenones, elemental sulfur, and ammonium acetate as a nitrogen source to obtain the hitherto challenging five-membered heterocycles. Functionalities such as halogen, trifluoromethyl, cyano, methylthio, and heteroaryl groups were well tolerated.

Primary Amine-Functionalized Mesoporous Phenolic Resin-Supported Palladium Nanoparticles as an Effective and Stable Catalyst for Water-Medium Suzuki-Miyaura Coupling Reactions.

Metal nanoparticles have been recognized and widely explored as unique catalysts for carbon-carbon coupling reactions. However, due to their extreme tendency to agglomeration, the generation and stabilization of metal nanoparticles in a porous matrix is an important research field. Herein, novel mesoporous phenolic resin-supported palladium nanoparticles (Pd@NH2-MPRNs) were prepared via direct anionic exchange followed by gentle reduction by using primary amine-functionalized ordered mesoporous phenolic resin as the support. The obtained Pd@NH2-MPRN material still possessed large surface area and ordered two-dimensional hexagonal mesoporous structure. Meanwhile, uniform and well-dispersed palladium nanoparticles were formed in the mesoporous channels, which could be attributed to an efficient complexation and stabilization effect derived from the primary amine groups. As a result, it can promote Suzuki coupling of less activated aromatic bromides to various biaryls in water with high conversion and selectivity. This excellent performance was attributed to small particle sizes, ordered mesopores, and a hydrophobic pore surface, which resulted in the decreased diffusion limitation and the increased active site accessibility. It is noted that it is competitive with the best palladium catalysts known for water-medium Suzuki coupling reaction, and it can be reused at least seven times without significant reduction in the catalytic efficiency, showing a good recyclability. Therefore, this work provides a new potential platform for designing and fabricating robust ordered mesoporous-polymer-supported metal nanoparticles for various catalytic applications.