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The interfacial and micellization behavior of three dicarboxylic mino acid-based nionic urfactants, abbreviated as AAS (-dodecyl derivative of -aminomalonate, -aspartate, and -glutamate) in combination with hexadecyltrimethylammonium bromide (HTAB) were investigated by surface tension, conductance, UV-vis absorption/emission spectroscopy, dynamic light scattering (DLS), and viscosity studies. Critical micelle concentration (CMC) values of the surfactant mixtures are significantly lower than the predicted values, indicating associative interaction between the components. Surface excess, limiting molecular area, surface pressure at the CMC, and Gibbs free energy indicate spontaneity of the micellization processes compared to the pure components. CMC values were also determined from the sigmoidal variation in the plot of micellar polarity and pyrene UV-vis absorption/emission intensities with surfactant concentration. The aggregation number, determined by static fluorescence quenching method, increases with decreasing mole fraction of the AAS (α), where the micelles are mainly dominated by the HTAB molecules. The size of the micelle increases with decreasing α, leading to the formation of larger and complex aggregates, as also supported by the viscosity studies. Micelles comprising 20-40 mol % AAS are highly viscous, in consonance with their sizes. Some of the mixed surfactant systems show unusual viscosity (shear thickening and increased viscosity with increasing temperature). Such mixed surfactant systems are considered to have potential in gel-based drug delivery and nanoparticle synthesis.
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http://dx.doi.org/10.1021/acs.langmuir.9b02895 | DOI Listing |
Molecules
July 2025
Faculty of Physics, Babes-Bolyai University, Str. M. Kogălniceanu 1, RO-400084 Cluj-Napoca, Romania.
1,3-Diphenylisobenzofuran (DPBF) is a widely used fluorescent probe for singlet oxygen (O) detection in photodynamic applications. In this work, we present an integrated experimental and computational analysis to describe its spectroscopic, photophysical, and reactive properties in ethanol, DMSO, and DMF. UV-Vis and fluorescence measurements across a wide concentration range show well-resolved S → S electronic transition of a π → π* nature with small red shifts in polar aprotic solvents.
View Article and Find Full Text PDFJ Phys Chem A
August 2025
Key Laboratory of Clusters Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, P. R. China.
In this study, the , Optoelectronic characteristics, and electronic circular dichroism (ECD) spectra of the supramolecular assembly of a perylene diimide analog having β- alanine at the amide positions (PDI(β-ala)) and guanosine-5'-monophosphate nucleotide (GMP) were studied experimentally and computationally. The investigation encompassed geometric characteristics, dipole moments, hyperpolarizabilities, frontier molecular orbitals (FMO), density of states (DOS), and spectral analysis. Interaction types were evaluated using noncovalent interactions, QTAIM topology analysis, and natural bonding orbitals.
View Article and Find Full Text PDFInorg Chem
July 2025
Pacific Northwest National Laboratory, 902 Battelle Blvd, Richland, Washington 99354, United States.
We report the preparation and optical characterization of three solutions of Am(III) in common aqueous (aq.) mineral acids (HCl, HNO, and HBr), including absorption, emission, and Raman vibrational analyses. To our knowledge, this study provides the first detailed absorption spectra of Am(III) spanning the entire UV/vis/NIR region in these mineral acids reported since the 1960s.
View Article and Find Full Text PDFChem Sci
July 2025
Institute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong Pokfulam Road Hong Kong PR China
A series of anionic alkynylplatinum(ii) complexes with terpyridine (tpy) or 2,6-bis(benzimidazol-2'-yl)pyridine (bzimpy) as the tridentate -donor pincer ligand has been synthesized and characterized. These complexes are found to form ensembles with a cationic poly(fluorene--phenylene) derivative (PFP-NMe ) through electrostatic, Pt(ii)⋯Pt(ii) and π-π stacking interactions. Förster resonance energy transfer (FRET) has been found to take place, consequently gave rise to fluorescence quenching of the polymer donor and the emergence of low-energy emission from the platinum(ii) complex assemblies.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
July 2025
Department of Physics, Faculty of Engineering and Natural Sciences, Manisa Celal Bayar University, TR-145140 Manisa, Turkey.
This paper explores the electronic structure and spectral characteristics of coumarin (C), C-6H, C-153, and C-343 in the protic polar solvent acetonitrile, combining computational methods via Density Functional Theory (DFT) and time-dependent Density Functional Theory (TD-DFT) with experimental analysis of UV-Vis and fluorescence spectra. The optoelectronic features of C, C-6H, C-153, and C-343 are primarily utilized in the solution phase for various applications, such as lasers and dye-sensitized solar cells. Computational studies were conducted using four different Modal Chemistry methods [MC1: CAM-B3LYP/6-311++G(d.
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