The excited state properties of three heteroleptic copper(I) xantphos 4H-imidazolate complexes are investigated by means of femtosecond and nanosecond time-resolved transient absorption spectroscopy in dichloromethane solution. The subpicosecond spectral changes observed after excitation into the MLCT absorption band are interpreted as intersystem crossing from the singlet to the triplet manifold. This interpretation is corroborated by DFT and TD-DFT results, indicating a comparable molecular geometry in the ground state (and hence the nonrelaxed singlet state) and the excited triplet state. Population of the triplet state is followed by planarization of the N-aryl rings of the 4H-imidazolate ligand on a 10 ps time scale. The planarization strongly depends on the substitution pattern of the N-aryls and correlates with the reduced moment of inertia for the planarization motion. The triplet state subsequently decays to the ground state in about 100 ns. These results demonstrate that the excited state processes of copper(I) complexes depend on the specific ligand(s) and their substitution pattern. Thus, the work presented points to a possibility to design copper(I) complexes with specific photophysical properties.
Secondary metabolites are key components in microbial ecology by mediating interactions between bacteria and their environment, neighboring species or host organisms. Bioactivities can be beneficial for both interaction partners or provide a competitive advantage only for the producer. Colonizers of confined habitats such as biofilms are known as prolific producers of a great number of bioactive secondary metabolites and are a potential source for novel compounds. We investigated the strain Paracoccus marcusii CP157, which originates from the biofilm on the carapace of a shell disease-affected Cancer pagurus specimen, for its potential to produce bioactive secondary metabolites. Its closed genome contains 22 extrachromosomal elements and several gene clusters potentially involved in biosynthesis of bioactive polyketides, bacteriocins, and non-ribosomal peptides. Culture extracts of CP157 showed antagonistic activities against bacteria from different phyla, but also against microalgae and crustacean larvae. Different HPLC-fractions of CP157 culture extracts had antibacterial properties, indicating that several bioactive compounds are produced by CP157. The bioactive extract contains several small, antibacterial compounds that partially withstand elevated temperatures, extreme pH values and exposure to proteolytic enzymes, providing high stability toward environmental conditions in the natural habitat of CP157. Further, screening of 17 Paracoccus spp. revealed that antimicrobial activity, hemolysis and production of N-acyl homoserine lactones are common features within the genus. Taking into account the large habitat diversity and phylogenetic distance of the tested strains, we hypothesize that bioactive secondary metabolites play a central role in the ecology of Paracoccus spp. in their natural environments.
In contrast to many other water birds, the Great Cormorant, Phalacrocorax carbo (Phalacrocoracidae), shows a typical wing-spreading behavior after diving. This behavior has been linked to the partial wettability of the Cormorant’s feathers based on the unusual structure of the contour feathers. Close to the rachis, these feathers have a closed vane with very densely spaced barbs but have an open vane in more peripheral feather parts. To investigate whether the wettability is connected to the composition of the uropygial gland secretion that is often linked to water repellency of bird feathers, we analyzed the gland secretions of the Great Cormorant and, for comparison, of the Muscovy Duck, Cairina moschata (Anatidae). Using the mass spectrometry techniques, atmospheric solids analysis probe-atmospheric pressure chemical ionization-mass spectrometry (ASAP-APCI-MS) and gas chromatography/mass spectrometry (GC/MS), significant differences in the chemical composition of the secretions were revealed. The Cormorant showed a highly diverse mixture of more than 1000 compounds consisting of methyl-branched aliphatic carboxylic esters with large chain length variability. In contrast, the duck’s secretion is dominated by the two esters octadecyl and eicosyl 2,4,6-trimethyloctanoate. Water contact angle measurements of the secretions showed that the secretion of the Muscovy Duck has higher water repellency than that of the Great Cormorant. Nevertheless, contact angle measurements of feathers before and after removing of feather waxes indicate that these waxes, likely consisting of the uropygial gland secretions, did not influence water repellency of the feathers to a large degree.
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