Structural analysis of natural deep eutectic solvents. Theoretical and experimental study (original) (raw)
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Journal of Molecular Liquids, 2021
In the current study, molecular dynamics simulations were conducted to investigate the structural and dynamical properties of glucose-based Deep Eutectic Solvents (DESs) at different molar ratios (the mixture of glucose and choline chloride with the molar ratios of 1:3, 1:1 and 3:1). Accordingly, the interaction energies of different species and structural properties such as atom-atom radial distribution functions (RDFs), the hydrogen-bonding network between species, and spatial distribution functions (SDFs) were computed to understand effective interactions in the eutectic mixture formation. It was found that the insertion of glucose molecules reduced the accumulation of chloride anions around choline cations, eventually decreasing the interaction between the choline chloride ion pairs. Moreover, the possible explanations for the thermos-physical properties of DESs, such as the shear viscosity and density, have been provided. Dynamical properties of DES were evaluated by calculating the mean-square displacement (MSD) and the velocity autocorrelation function (VACF) for the centers of the mass of the ions and glucose molecules. MSD analysis results were then used to calculate the self-diffusion parameter by applying the Einstein relation. The simulation results indicated that increasing the temperature led to easing the migration of the molecules and decreasing the dependence of the movement of the molecules on each other. This growing trend of migration may lead to an increase in the self-diffusion coefficient of molecules. Structural analysis revealed that a ratio of 1:1 of glucose: choline chloride could provide the best condition to maintain the low melting point of the mixture due to the strong hydrogen-bonded network between the two species.
2022
In our work, we have studied the formation of choline chloride based NADESs using DFT calculations, and all-atom classical Molecular Dynamics (MD) simulations. In our DFT calculations, the ground state geometry optimizations were performed in the gas phase using DFT B3LYP 6-31+G(d) level of theory. Moreover, all-atom classical Molecular Dynamics simulations were implemented using Gromos force eld. The DFT calculation results revealed the formation of NADESs via formation (creation) of binding between chlorine and choline, and chlorine and glucose. Next, the results of all-atom classical Molecular Dynamics simulations, based on the time average of the equilibrated production run of MD simulations, stated that the nitrogen atom of choline ion, and chloride ion have greater interactions, while chloride ion have also greater interaction with glucose during formation of NADES. Highlights Intermolecular interactions of NADES were studied by DFT calculations and all-atom classical Molecular Dynamics simulations.
Fluid Phase Equilibria, 2017
Several novel applications of Deep Eutectic Solvents (DESs) have emerged recently. With a growing interest in the field, there is an urge to understand formation and functioning of these solvents at molecular level, which in turn would assist in further designing of DESs. We herein performed molecular dynamics simulations on three of the commonly used type III DES, viz, reline, ethaline, and glyceline, which are mixtures of urea, ethylene glycol, and glycerol with choline chloride at eutectic composition. Our results explain the role of inter-molecular and intra-molecular hydrogen bonding and energies on formation of these DESs. Furthermore, the ability of these DESs to be altered in a desired way through a simple addition of water makes it versatile solution for several other applications. Hence, simulations are also performed on the aqueous DES solutions, which reveal the effect of water on intermolecular network of interaction existing within these DESs.
Journal of Chemical & Engineering Data, 2017
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Tailoring properties of natural deep eutectic solvents with water to facilitate their applications
Food Chemistry, 2015
Previously it was demonstrated that natural deep eutectic solvents (NADES) are promising green solvents for the extraction of natural products. However, despite their potential, an obvious disadvantage of NADES is the high viscosity. Here we explored the dilution effect on the structures and physicochemical properties of NADES and their improvements of applications using quercetin and carthamin. The results of FT-IR and 1 H NMR experiments demonstrated that there are intensive H-bonding interactions between the two components of NADES and dilution with water caused the interactions weaken gradually and even disappeared completely at around 50% (v/v) water addition. A small amount of water could reduce the viscosity of NADES to the range of water and increase the conductivity by up to 100 times for some NADES. This study provides the basis for modulating NADES in a controllable way for their applications in food processing, enzyme reactions, pharmaceuticals and cosmetics.
Glucose-based deep eutectic solvents: Physical properties
Journal of Molecular Liquids, 2013
Deep eutectic solvents (DESs) are considered nowadays as green ionic liquid (IL) analogues. Despite their relatively short period of introduction as a special class of ILs, they have been under an increasing emphasis by the scientific community due to their favorable properties. In the present study, a glucose based DES of choline chloride (2-hydroxyethyl-trimethylammonium chloride) with the monosaccharide sugar D-glucose anhydrous was synthesized at different molar ratios. The physical properties of density, viscosity, surface tension, refractive index, and pH were measured and analyzed as function of temperature in the practical temperature range of 298.15-358.15 K. The analysis of these physical properties revealed that these novel DESs have the potential to be utilized for several possible industrial applications involving processing and separation of food constituents, pharmaceutical applications, as well as mediums for chemical reactions.
Journal of Molecular Structure, 2017
The in-silico combination mechanism of triethylene glycol based DESs has been studied. COSMO-RS and graphical user interface TmoleX software were used to predict the interaction mechanism of hydrogen bond donors (HBDs) with hydrogen bond acceptors (HBA) to form DESs. The predicted IR results were compared with the previously reported experimental FT-IR analysis for the same studied DESs. The sigma profiles for the HBD, HBAs and formed DESs were interpreted to identify qualitatively molecular properties like polarity or hydrogen bonding donor and acceptor abilities. The predicted physicochemical properties reported in this study were in good agreement with experimental ones.
Los solventes eutécticos profundos son mezclas compuestas típicamente por un donador de puentes de hidrógeno y un aceptor de puentes de hidrógeno. Han aparecido como una alternativa de los líquidos iónicos en varios procesos debido a su capacidad de adaptación, biodegradabilidad y bajo costo. Recientemente, los solventes eutécticos profundos se han estudiado como solventes potenciales para diferentes aplicaciones. Entonces, sus propiedades fisicoquímicas deben caracterizarse para comprender la interacción entre sus componentes y con otros compuestos. Los solventes eutécticos profundos preparados para este trabajo se basaron en cloruro de colina mezclado con etilenglicol, 1,3-propanodiol o 1,4-butanodiol en una relación molar de 1:3. Se realizan diferentes familias de DES basadas en cloruro de colina y betaína en paralelo para generar una base de datos, ver el ajuste y la predicción utilizando el modelo de esfera dura. La densidad y la viscosidad de los disolventes eutécticos profund...
Deep Eutectic Solvents: A Review of Fundamentals and Applications
Chemical Reviews, 2021
Deep eutectic solvents (DESs) are an emerging class of mixtures characterized by significant depressions in melting points compared to those of the neat constituent components. These materials are promising for applications as inexpensive "designer" solvents exhibiting a host of tunable physicochemical properties. A detailed review of the current literature reveals the lack of predictive understanding of the microscopic mechanisms that govern the structure−property relationships in this class of solvents. Complex hydrogen bonding is postulated as the root cause of their melting point depressions and physicochemical properties; to understand these hydrogen bonded networks, it is imperative to study these systems as dynamic entities using both simulations and experiments. This review emphasizes recent research efforts in order to elucidate the next steps needed to develop a fundamental framework needed for a deeper understanding of DESs. It covers recent developments in DES research, frames outstanding scientific questions, and identifies promising research thrusts aligned with the advancement of the field toward predictive models and fundamental understanding of these solvents. CONTENTS
Fruit sugar-based deep eutectic solvents and their physical properties
Thermochimica Acta, 2012
In this study, a novel fructose-based DES of choline chloride (2-hydroxyethyl-trimethylammonium) has been synthesized at different molar ratios. The physical properties such as density, viscosity, surface tension, refractive index and pH were measured and analyzed as function of various temperatures (25-85 • C). The analysis of these physical properties revealed that these new DESs have the potential to be utilized for possible industrial applications involving processing and separation of food constituents. The suggested DESs have many desirable characteristics, e.g. they have low vapor pressure, inflammable, biodegradable, and made from renewable resources. The use of these DESs will positively affect the environment and make use of available renewable resources.