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The combined NMR and quantum chemical study of tellurium solution in trioctylphosphine, for the first time, revealed the new unexpected P−Te species. The observed intermediates are absolutely different from the species forming in the reaction of trialkylphosphines with chalcogens up in the group. This finding sheds new light on the mechanism of telluride nanocrystals formation and allow to rationalize the application of this key tellurium precursor in the synthesis of nanostructures. The studied solution was applied in the synthesis of HgTe colloidal quantum dots. [ABSTRACT FROM AUTHOR]

Formation of reverse micelles in the water-hexane-AOT system has been investigated by molecular dynamics simulations. In order to optimize calculation strategy, the starting spatial disposition of components was assumed to be random. Such an approach was found to provide a lower dependence of final results on initial conditions as compared to the calculations using pre-assembled reverse micelles as a starting geometry. The calculated structural parameters of reverse micelles (such as their shape, size, and distribution of components) were found to agree with the available experimental data. [ABSTRACT FROM AUTHOR]

The photoluminescence from n-hexane solutions of the dyes obtained by the introduction of amino groups into the meta position of the phenyl rings of 3,5-diphenyl-8-CF 3 -BODIPY was found to be strongly quenched by some aromatic molecules (benzene and toluene). On the contrary, the introduction of an amino group into the para position does not lead to significant quenching. The quenching of photoluminescence from the meta derivatives obeys the mixed static + dynamic mechanism. Temperature-dependent time-resolved fluorescence measurements were performed to determine the Stern-Volmer constants of the static and dynamic components of quenching. It follows from these data that the binding energy between luminophore and toluene molecules is about 5.0 kcal/mol in the ground state and larger than 3.4 kcal/mol in the excited state. Complexation with toluene facilitates the intramolecular charge transfer in the BODIPY derivatives with the meta position of the amino groups, resulting in photoluminescence quenching., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021. Published by Elsevier B.V.)