In the following paper, a Re(I) complex with electron-withdrawing oxadiazole group in its diamine ligand (denoted as N-N) was synthesized. Its single crystal structure analysis confirmed the successful synthesis of both ligand and complex. The central Re(I) ion localized in a traditional octahedral coordination environment. The diamine ligand 2-(pyridin-2-yl)-5-(p-tolyl)-1,3,4-oxadiazole (denoted as PPOZ) took a coplanar structure and the corresponding face-to-face π-π attraction between PPOZ ligands made the Re(I) complex molecules adjust a highly ordered arrangement which was positive to improve emissive performance. In order to repress the excited state geometric relaxation and further improve the emissive performance, the Re(I) complex was doped into a polymer host poly(vinylpyrrolidone) via electrospinning, resulting in composite fibers. The morphology of those composite fibers was analyzed by electron microscopy. The photophysical comparison between bulk sample and composite fibers indicated that the composite fibers showed emission blue shift, longer excited state lifetime and improved photostability. Further analysis suggested that the excited state geometric relaxation could be effectively repressed when the Re(I) complex molecules were immobilized in the polymer matrix, leading to above variations.
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http://dx.doi.org/10.1016/j.saa.2013.11.022 | DOI Listing |
Dalton Trans
January 2025
Institute of Chemistry, Faculty of Science and Technology, University of Silesia, Szkolna 9, 40-006 Katowice, Poland.
Over the last five decades, diimine rhenium(I) tricarbonyl complexes have been extensively investigated due to their remarkable and widely tuned photophysical properties. These systems are regarded as attractive targets for design functional luminescent materials and performing fundamental studies of photoinduced processes in transition metal complexes. This review summarizes the latest developments concerning Re(I) tricarbonyl complexes bearing donor-acceptor (D-A) and donor-π-acceptor (D-π-A) ligands.
View Article and Find Full Text PDFInt J Mol Sci
December 2024
Department of OB/GYN and REI (UniKiD), Medical Faculty and University Hospital Duesseldorf, Heinrich Heine University Duesseldorf, 40255 Duesseldorf, Germany.
To date, very little is known about how apoptosis and autophagy affect human endometrial stromal cells (ESCs), particularly how these processes might determine the depth of implantation in humans. Before investigating how apoptosis and autophagy might modulate the implantation process in an infertile population, it is necessary to clarify how these processes are regulated in healthy individuals. This study examined the protein expression related to apoptosis and autophagy in primary ESCs from fertile women, particularly in the context of decidualization and embryo contact, using Western blot analysis.
View Article and Find Full Text PDFCell Biol Toxicol
January 2025
Lab. Genetics and Molecular Bases of Complex Diseases, Health Research Institute of Hospital Clínico San Carlos (IdISSC), 28040, Madrid, Spain.
The underlying mechanisms explaining the differential course of SARS-CoV-2 infection and the potential clinical consequences after COVID-19 resolution have not been fully elucidated. As a dysregulated mitochondrial activity could impair the immune response, we explored long-lasting changes in mitochondrial functionality, circulating cytokine levels, and metabolomic profiles of infected individuals after symptoms resolution, to evaluate whether a complete recovery could be achieved. Results of this pilot study evidenced that different parameters of aerobic respiration in lymphocytes of individuals recuperated from a severe course lagged behind those shown upon mild COVID-19 recovery, in basal conditions and after simulated reinfection, and they also showed altered glycolytic capacity.
View Article and Find Full Text PDFSci Rep
December 2024
KAUST Center of Excellence for Smart Health (KCSH), King Abdullah University of Science and Technology, Thuwal, 23955, Saudi Arabia.
Analyzing microbial samples remains computationally challenging due to their diversity and complexity. The lack of robust de novo protein function prediction methods exacerbates the difficulty in deriving functional insights from these samples. Traditional prediction methods, dependent on homology and sequence similarity, often fail to predict functions for novel proteins and proteins without known homologs.
View Article and Find Full Text PDFComput Biol Chem
December 2024
Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar, Gujarat 388 120, India. Electronic address:
A series of substituted 2-(2-benzylidenehydrazinyl)benzothiazole Schiff-base derivatives and complexes containing Re(I) were synthesized and analyzed using various characterization techniques, including elemental analysis, conductance measurement, H-NMR, FT-IR, and LC-MS. The biological activities of the compounds were evaluated. Binding affinity between the complexes and calf thymus DNA (CT-DNA) was conducted using UV-visible spectroscopy, viscosity measurement, fluorescence spectroscopy, and molecular docking studies, indicating intercalation binding mode.
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