Exciplexes of 2,6,9,10-tetracyanoanthracene (TCA) with alkylbenzenes were investigated in solvents ranging from cyclohexane to acetonitrile. Plots of the reduced emission maxima or the average emission frequency (hν) versus redox potential differences (E) were linear with a slope of ∼1 in all solvents, which is consistent with the highly ionic character of the exciplexes. The exciplex spectra were analyzed in terms of the energy gap between the exciplex minimum and the AD pair (ΔG), the energy difference between ΔG and E (δ), and the total reorganization energy (Σλ). A plot of (E - hν), equivalent to (Σλ - δ), versus a solvent polarity function showed a linear dependency for the low-to-moderate polarity solvents, whereas highly polar solvents deviated significantly. δ showed a smooth linear dependency for all solvents. Thus, the deviation of the polar solvents is due to a larger-than-expected Σλ. Additionally, the full width at half-maximum (fwhm) of the emission spectra in polar solvents deviates significantly from the extrapolated trend in less-polar solvents. The deviations of Σλ and fwhm in highly polar solvents can plausibly be explained by composite emissions from two exciplex structures, with the donor overlapping with the inner or outer ring of TCA.
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http://dx.doi.org/10.1021/acs.jpca.7b01461 | DOI Listing |
ACS Nano
January 2025
School of Science and Engineering, Shenzhen Institute of Aggregate Science and Technology, The Chinese University of Hong Kong, Shenzhen (CUHK-Shenzhen), Guangdong 518172, P.R. China.
Helical structures such as right-handed double helix for DNA and left-handed α-helix for proteins in biological systems are inherently chiral. Importantly, chirality at the nanoscopic level plays a vital role in their macroscopic chiral functionalities. In order to mimic the structures and functions of natural chiral nanoarchitectures, a variety of chiral nanostructures obtained from artificial helical polymers are prepared, which can be directly observed by atomic force microscopy (AFM), scanning tunneling microscopy (STM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM).
View Article and Find Full Text PDFBiomed Chromatogr
February 2025
Department of Pharmaceutical Chemistry and Analysis, ISF College of Pharmacy, Moga, Punjab, India.
Enantioseparation and enantiorecognition are crucial in the pharmaceutical analysis of chiral substances, impacting safety, efficacy, and regulatory compliance. Enantioseparation refers to the process of separating enantiomers from a mixture, typically achieved through chromatography techniques like HPLC and SFC. In contrast, enantiorecognition involves the identification of enantiomers based on their interaction with a chiral selector without the need for separation.
View Article and Find Full Text PDFLangmuir
January 2025
Biomimetic Materials and Tissue Engineering Laboratory, Department of Chemical Engineering, University of South Carolina, Columbia, South Carolina 29208, United States.
The self-assembly of phenylalanine (F)-based peptides is a critical area of research with potential implications for the development of advanced biomaterials and technologies. Previous studies indicate that homo-oligopeptides with F-X residues (X = 1 to 6) can self-assemble into diverse nano-microstructures, but the role of oligopeptide chain length on this process remains unclear. This review investigates the role of F-X chain length on self-assembly processes and morphologies, considering the effect of incubation conditions and the capping group at the N and/or C terminals.
View Article and Find Full Text PDFCompelling concerns about antimicrobial resistance and the emergence of multidrug-resistant pathogens call for novel strategies to address these challenges. Nanoparticles show promising antimicrobial activities; however, their actions are hindered primarily by the bacterial hydrophilic-hydrophobic barrier. To overcome this, we developed a method of electrochemically anchoring sodium dodecyl sulfate (SDS) coatings onto silver nanoparticles (AgNPs), resulting in improved antimicrobial potency.
View Article and Find Full Text PDFChemistry
December 2024
Technological University Dublin, Institute of Polymers, Kevin Street, Dublin 8, Dublin, IRELAND.
Donor-acceptor BODIPY dyads, functionalized at the 2 and 6 positions with benzyl ester (BDP-DE) or carboxylic acid (BDP-DA) groups, were synthesized and characterized for their optoelectronic properties. The introduction of carbonyl groups increased the reduction potential of the BODIPY core by 0.15-0.
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