Publications by authors named "P M Tolstoy"

In this computational work we study complexes with two equivalent intermolecular hydrogen bonds formed between trimethyl phosphine oxide and two identical proton donors ("twin" hydrogen bonds) for a set of 70 proton donor molecules. The changes in the phosphorus chemical shift and stretching frequency of the PO group upon complexation correlate quite well with the total strength of two hydrogen bonds. A set of explicit numerical dependences is proposed for assessing interatomic distances and hydrogen bond strengths from spectral data.

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Background: Deep eutectic solvents (DES) have emerged as effective solvents that address many challenges in analytical chemistry, particularly in microextraction. However, until now, their use has been primarily focused on extraction processes. This has significantly limited their application in analytical chemistry, especially in flow analysis, where the high viscosity of DES has made their use difficult.

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The Morse function is the simplest anharmonic approximation of the potential of a diatomic molecule, for which the vibrational Schrödinger equation could be solved almost precisely. Despite its crudeness, the Morse function has been widely used in solving various problems in molecular spectroscopy. In recent years, special attention was paid to the existence of two Morse approximations for the electronic terms U(r) of diatomic molecules, M1(r) and M2(r), which differ by the selection of primary fitting parameters and satisfactorily reproduce different parts of U(r).

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In this work, a novel deep eutectic solvent (DES) composed of thymol and 1-(o Tolyl)thiourea 9/1 (mol) is presented for the first time. This DES has not been described in the literature. This DES was first used as a stationary phase in an extraction column integrated into a flow injection analysis system for the simultaneous determination of mercury and copper in edible oils.

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Article Synopsis
  • The study examined a composite material made of silica aerogel and flufenamic acid (FFA) using various nuclear magnetic resonance (NMR) techniques to understand its structural and sorption properties.
  • Magic angle spinning NMR revealed strong interactions between the aerogel and FFA, while solid-state NMR provided information on the aerogel's stability and confirmed FFA's presence within the composite.
  • Results showed that the inclusion of FFA altered the aerogel's pore structure and sorption characteristics, which is important for creating new solid drug forms.
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