An aggregation-induced emission enhancement (AIEE) effect in fluorescent lipophilic 2,1,3-benzothiadiazole (BTD) derivatives and their organic nanoaggregates were studied. A set of techniques such as single-crystal X-ray, dynamic light scattering (DLS), electron paramagnetic resonance (EPR), UV-vis, fluorescence, and density functional theory (DFT) calculations have been used to decipher the formation/break (kinetics), properties, and dynamics of the organic nanoaggregates of three BTD small organic molecules. An in-depth study of the excited-state also revealed the preferential relaxation emissive pathways for the BTD derivatives and the dynamics associated with it. The results described herein, for the first time, explain the formation of fluorescent BTD nanoaggregate derivatives and allow for the understanding of their dynamics in solution as well as the ruling forces of both aggregation and break processes along with the involved equilibrium. One of the developed dyes could be used at a nanomolar concentration to selectively stain lipid droplets emitting an intense and bright fluorescence at the red channel. The other two BTDs could also stain lipid droplets at very low concentrations and were visualized preferentially at the blue channel.
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http://dx.doi.org/10.1021/acs.joc.0c01805 | DOI Listing |
J Photochem Photobiol B
December 2024
Department of Health Sciences, Federal University of Espírito Santo, São Mateus 29932-540, Brazil. Electronic address:
The heightened susceptibility to skin cancer correlates with exposure to ultraviolet (UV) radiation, which can induce various cutaneous injuries. Inorganic UV filters, like zinc oxide (ZnO), are extensively utilized in sunscreens owing to their capacity to scatter and reflect UV radiation. The efficacy of inorganic UV filters can be augmented across a wider spectrum through synergistic combinations with other active compounds, such as organic UV filters.
View Article and Find Full Text PDFAnal Chem
December 2024
Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, P. R China.
Herein, the bovine serum albumin (BSA)-loaded tetrakis[4-(4'-cyanophenyl)phenyl]ethane nanoaggregates (NAs) (BSA@TBPE-(CN) NAs) as a novel electrochemiluminescence (ECL) emitter were first prepared, which exhibited superior ECL performance via the newly defined protein-induced ECL enhancement. Impressively, BSA not only restricted the intramolecular motions by its hydrophobic cavity to improve optical radiation for enhancing ECL efficiency but also promoted the electrochemical excitation of BSA@TBPE-(CN) NAs in which amino acid residues of BSA altered the surface states and narrowed the energy gap of BSA@TBPE-(CN) NAs for further boosting the ECL efficiency. Furthermore, the BSA@TBPE-(CN) NAs displayed a more dispersed state due to electrostatic repulsion caused by its considerable negative charges, which was conducive to reacting more fully with coreactants for improving ECL emission.
View Article and Find Full Text PDFSensors (Basel)
November 2024
IBB-Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, 1049-001 Lisboa, Portugal.
Langmuir
December 2024
Center for Surface- and Nanoanalytics (ZONA), Johannes Kepler University Linz, Altenberger Str. 69, 4040 Linz, Austria.
Organic molecular beam deposition (OMBD) of -hexaphenylene (p6P) on polycrystalline platinum results in the formation of unique nanoaggregates, predominantly as nanofibers and nanoribbons. These aggregates exhibit distinct morphological properties, as revealed by atomic force microscopy (AFM). Grazing incidence X-ray diffraction (GIXD) confirms the p6P herringbone structure as partially oriented aggregates with a bias of previously observed contact planes parallel to the substrate.
View Article and Find Full Text PDFLangmuir
November 2024
College of Chemical and Biological Engineering, Shandong University of Science and Technology, Qingdao 266590, P R China.
The liquid-liquid interface offers a confined space to control the growth of nanomaterials. In this study, Fe(II) (water phase) induced Meso-tetra (4-carboxyphenyl) porphyrin (HTCPP) (CHCl, organic phase) into nanoaggregates (Fe-TCPP) in the liquid-liquid interface. By tuning the ratio of DMF in organic solvents, Fe(II) induced HTCPP into two nanoaggregates (Fe-TCPP-1 and Fe-TCPP-2) with different morphologies via coordination interaction occurring at the water-CHCl interface.
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