Synthesis of a Palladium Dimer Supported by a C-Bound Trifluoroacetonate Bridge Formed by Cleavage of a Hexafluoroacetylacetonate Ligand.

Palladium(II) hexafluoroacetylacetonate (Pd(Hfacac)) is known to form adducts of bases, such as lutidine (2,6-dimethylpyridine). When treated with approximately 3 equiv of lutidine, Pd(Hfacac) yields a 1:1 complex as reported in the literature, Pd(,-Hfacac)(-Hfacac)(lutidine), . However, when the amount of excess lutidine is increased, a new complex, , is formed.

Mode-hop-free tunable high-power distributed feedback laser with adaptable rear facet phase shift section emitting at 780 nm.

We present a high-power ridge waveguide distributed feedback (DFB) laser with a high-reflective coating and a phase shift section at the rear facet. The phase shift section is realized by means of a micro heater that is placed parallel to the ridge waveguide and the uniform grating. This type of heater section is easy to integrate into existing laser designs and allows adjusting and controlling the spectral behavior of the distributed feedback laser by shifting the rear facet phase condition, which makes it possible to overcome the challenges of mode-hop-free tuning of regular DFB lasers with highly reflective cleaved rear facet.

Magnetically Guided Adeno-Associated Virus Delivery for the Spatially Targeted Transduction of Retina in Eyes.

Adeno-associated viruses (AAVs) are intensively explored for gene therapies in general and have found promising applications for treating retina diseases. However, controlling the specificity (tropism) and delivery of AAVs to selected layers, cell types, and areas of the retina is a major challenge to further develop retinal gene therapies. Magnetic nanoparticles (MNPs) provide effective delivery platforms to magnetically guide therapeutics to target cells.

Ablation of integrin-mediated cell-collagen communication alleviates fibrosis.

Objectives: Activation of fibroblasts is a hallmark of fibrotic processes. Besides cytokines and growth factors, fibroblasts are regulated by the extracellular matrix environment through receptors such as integrins, which transduce biochemical and mechanical signals enabling cells to mount appropriate responses according to biological demands. The aim of this work was to investigate the in vivo role of collagen-fibroblast interactions for regulating fibroblast functions and fibrosis.