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1.
Molecules ; 29(17)2024 Aug 29.
Artículo en Inglés | MEDLINE | ID: mdl-39274950

RESUMEN

Polarizable continuum methods (PCM) have been widely employed for simulating solvent effects, in spite of the fact that they either ignore specific interactions in solution or only partially reproduce non-specific contributions. Examples of three solvatochromic dyes with a negative, a positive and a reverse behavior illustrate the achievements and shortcomings of PCM calculations and the causes for their variable success. Even when qualitatively mimicking non-specific solvent effects, departures of calculated values from experimental data may be significant (20-30%). In addition, they can utterly fail to reproduce an inverted behavior that is caused by significant specific contributions by the solvent. As shown through a theoretical model that rationalizes and predicts the solvatochromism of phenolate merocyanines based on DFT (Density Functional Theory) descriptors in the gas phase, PCM shortcomings are to be held responsible for its eventual failure to reproduce experimental data in solution.

2.
Magn Reson Chem ; 2024 Aug 27.
Artículo en Inglés | MEDLINE | ID: mdl-39192563

RESUMEN

The 1H and 13C NMR spectra of the N-(3,5-dichloro-4-hydroxyphenyl)- 2,4,6-triphenylpyridinium perchlorate and of its deprotonated betaine 4-(2,4,6-triphenylpyridinio)-2,6-dichlorophenolate (Wolfbeis's ET(33) dye) were recorded in various solvents and analyzed in search of solvent-dependent shifts that characterize their solvatomagnetism, which was compared with the well-known UV-vis spectral behavior of this important solvatochromic dye. Although the NMR spectra of ET(33) and its phenolic precursor in different solvents correlated only poorly with their UV-vis spectral responses, they provided valuable information on specific structural features and solute-solvent interactions that are not available from their UV-vis spectra.

3.
J Phys Chem B ; 128(29): 7208-7218, 2024 Jul 25.
Artículo en Inglés | MEDLINE | ID: mdl-38989920

RESUMEN

The ability of polarizable continuum models (PCM) to simulate nonspecific solvent effects (dipolarity and polarizability) was evaluated by calculating the transition energies of 1,1,10,10-tetrabutyldecanonaene (ttbp9) and 2-N,N-dimethylamino-7-nitrofluorene (DMANF), basis of Catalán's polarizability (SP) and dipolarity (SdP) solvent scales, respectively. Time-dependent density-functional theory (TD-DFT) calculations were performed at different levels of theory, employing four basis sets in 10 different solvents, covering the full range of the normalized SP and SdP scales. Transition energies were calculated using linear response (LR) and corrected linear response (cLR2) schemes. Although these methods yielded variable mean absolute errors, the LR-PCM calculations reproduced medium polarizability and dipolarity trends. While calculated ttbp9 transition energies correlated with SP and Laurence's dispersion-induced (DI) scales, the DMANF transition energies correlated poorly with SdP or Laurence's ES dipolarity scales. This result agrees with the fact that DMANF solvatochromism is "contaminated" by solvent polarizability and HB acidity. The incorporation of SP or DI contributions led to much better (r2 > 0.95) correlations with the DMANF-calculated transitions. The results offer a clearer picture of the limitations of continuum models in simulating the behavior of solvatochromic dyes in solution by pointing out their poor performance when specific solvent effects, such as hydrogen-bond interactions, play a significant role in their solvatochromism.

4.
Int J Biol Macromol ; 211: 490-498, 2022 Jun 30.
Artículo en Inglés | MEDLINE | ID: mdl-35569683

RESUMEN

Solutions of a pure organic solvent acidified with 1% sulfuric acid, and some of their aqueous mixtures were used for lignin extraction in the Pinus radiata sawdust delignification. Organic acid solvents including acetic, lactic and citric acids as well as non-acidic compounds such as γ-valerolactone, 2-methyltetrahydrofuran, glycerol and ethylene glycol were studied. Crude lignin extractions yields (%) ranging between ca. 5-50% were obtained, from which ethylene glycol (33%), γ-valerolactone (48%) and propylene carbonate (52%) showed the greatest effectiveness. The effect of added water on the lignin extraction was investigated in mixtures of an organic solvent with a variable water content (75%w/w, 50% w/w, 25%w/w and 10% w/w) where it was observed that the yield of extraction decreased with the increased water content. Moreover, the purity of extracted lignins were analyzed by spectroscopic methods (UV and IR). Kamlet-Taft solvent polarity parameters, were determined with the solvatochromic probes 4-nitroaniline, N,N-diethyl-4-nitroaniline, Nile Red and 6-propionyl-2-N,N-dimethylaminonaphthalene (PRODAN), and then correlated to lignin extraction yields to explain the influence of the solute-solvent interactions on biomass delignification. A reasonable correlation was found between the medium polarizability-dipolarity π* and the effectiveness of the solvent mixture on the extraction of lignin wood.


Asunto(s)
Lignina , Madera , Glicol de Etileno , Lignina/química , Solventes/química , Agua/química , Madera/química
5.
Materials (Basel) ; 14(21)2021 Oct 20.
Artículo en Inglés | MEDLINE | ID: mdl-34771765

RESUMEN

Three photobicyclized benzodithienoquinolizinium tetrafluoroborates (BPDTQBF4) were prepared and evaluated by UV-Vis and fluorescence spectral, electrochemical analysis, and by theoretical calculations as possible organic n-type semiconductors. Evaluation and comparison of their LUMO levels, HOMO-LUMO energy gaps as monomeric and π-stacked dimers with those of other materials, suggest their potential as organic n-type semiconductors. Calculations of their relative charge carrier mobilities confirmed this potential for one derivative with a long (C-14) alkyl chain appended to the polycyclic planar π-system.

6.
ACS Omega ; 6(25): 16553-16564, 2021 Jun 29.
Artículo en Inglés | MEDLINE | ID: mdl-34235327

RESUMEN

Two parameters are introduced, a nonideality index (NII) and a nonideality area (NIA), for the analysis of the variations of thermodynamic properties of binary mixtures. Their calculation is based, for the NII, on experimental plots of the variation of a given property (density, refractive index, viscosity, etc.), and for the NIA, on experimental plots of its excess value (excess enthalpies, molar volumes, viscosities, refractive indices, isentropic compressibilities, etc.) with the mixture composition. Both nonideality parameters are therefore not based on any theoretical model or on its derived parameters, being applicable with any fitting equation. The NII or NIA values for a thermodynamic property of a series of related binary mixtures reveal interesting trends, which are not evident in most analyses of such systems. Besides their predictive value, these trends provide information on the relevance of solvent characteristics of the binary mixture, thus supporting new insights or interpretations of the experimental data.

7.
Spectrochim Acta A Mol Biomol Spectrosc ; 229: 118008, 2020 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-31923787

RESUMEN

The positive solvatochromism of three dyes, with a spectral behavior strongly dependents on the medium dipolarity/polarizability, was studied theoretically. Both a polarizable continuum-solvent model (CSM) and explicit solvent molecules were employed to model solvent effects. The CSM approach, coupled with ten different TDDFT methods, yielded unsatisfactory results in eleven solvents. The explicit-solvation calculations, thought of much higher computational cost, yielded excellent results. As CSM schemes are known correctly model non-specific electrostatic effects, our results indicate that the traditionally considered non-specific nature of solvent dipolarity needs to be reconsidered, requiring the explicit consideration of the solute-solvent interactions for their accurate theoretical description.

8.
Spectrochim Acta A Mol Biomol Spectrosc ; 222: 117264, 2019 Nov 05.
Artículo en Inglés | MEDLINE | ID: mdl-31212193

RESUMEN

The positive halochromism of the solvatochromic 4-nitro-4'-(N,N-dimethylamino)-2,2'-bithiophene in acetone and 1-butanol was investigated by molecular dynamics simulations and quantum mechanics calculations. Interactions of the dye with the solvated sodium cation were found to have only a minor effect on the observed halochromism, which was ultimately ascribed to a predominant interaction between iodide anions and the N,N-dimethylamino group of the dye.

9.
Food Chem ; 279: 288-293, 2019 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-30611492

RESUMEN

A protocol for determining the location of antioxidants (AOs) in a micro-heterogeneous medium was applied to three series of AOs with increasing hydrophobicities: chromancarboxylic acid ("Trolox") esters, caffeic acid and its esters, and gallic acid and its esters. The observed paradoxical behaviour of these and other commonly encountered antioxidants was rationalized with the aid of a pictorial simile, the "diving-swan" analogy, that explains the orientation and location of an amphiphobic AO when it reacts with a radical probe in the micellar interface.


Asunto(s)
Antioxidantes/química , Ácidos Cafeicos/química , Cromanos/química , Ácido Gálico/química , Micelas , Antioxidantes/análisis , Ésteres/química , Interacciones Hidrofóbicas e Hidrofílicas
10.
Photochem Photobiol ; 94(6): 1100-1108, 2018 11.
Artículo en Inglés | MEDLINE | ID: mdl-29984405

RESUMEN

Seven new 2,4,6-triarylpyrimidines were synthesized and their solvatofluorochromism investigated in 12 solvents and in an aqueous micellar solution of reduced Triton X-100. A multiparametric analysis of their emission band showed that the solvent dipolarity and basicity were mainly responsible for their solvatofluorochromism, which arose from an internal charge-transfer from a donor fragment to the pyrimidine acceptor, confirmed by theoretical calculations. In the micellar system, quenching of their fluorescence by addition of derivatives of 2,2,6,6-tetramethylpiperidinoxyl (TEMPO) radical was investigated and the results were consistent with the spectral changes brought about by the micro-heterogeneous system.

11.
Food Chem ; 245: 240-245, 2018 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-29287366

RESUMEN

A simple protocol is described for locating the site of action of an antioxidant (AO) in a micro-heterogeneous mixture, based on the pattern of the reactivity curve towards the AO of a series of 4-alkanoyl TEMPO radicals. The resulting cut-off curves yield information regarding the hydrophobic microenvironment surrounding the reactive AO group, and its accessibility by the probe. Convex curves are an indication of an AO located in a more hydrophilic environment, while concave plots originate from AOs in a more hydrophobic location in the micro-heterogeneous system.


Asunto(s)
Antioxidantes/análisis , Antioxidantes/química , Emulsiones/química , Óxidos N-Cíclicos/química , Espectroscopía de Resonancia por Spin del Electrón , Interacciones Hidrofóbicas e Hidrofílicas , Micelas
12.
Food Chem ; 224: 342-346, 2017 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-28159277

RESUMEN

Three oil-in-water emulsions were prepared from mixtures of olive oil and Tween 20 in water. The effectiveness of a series of radical 2,2,6,6-tetramethylpiperidinoxyl (TEMPO) derivatives of variable lipophilicity in reactions with antioxidant Trolox, and as pyrene-fluorescence quenchers, was compared in the three emulsions. A "cut-off" effect was observed for the pyrene quenching by the probes, but not for their reaction with Trolox. The results were rationalized in terms of the amphiphobic nature of the probes, and the different locations of probe, pyrene and Trolox in the three-phase microheterogeneous systems.


Asunto(s)
Emulsiones/química , Aceite de Oliva/química , Agua/química , Antioxidantes/química , Cromanos/química , Polisorbatos , Pirenos/química
13.
Spectrochim Acta A Mol Biomol Spectrosc ; 173: 556-561, 2017 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-27780125

RESUMEN

The cationic halochromism and thermohalochromism of four phenolate dyes conjugated with aryl moieties substituted with one or two nitro groups were investigated in the presence of organic (tetra-n-butylammonium bromide and benzyltriethylammonium chloride) and inorganic (sodium perchlorate) salts, in hydrogen-bond donating (water, 1-propanol, 1-butanol and 2-propanol) and hydrogen-bond accepting (acetonitrile and dimethylsulfoxide) solvents. Although a positive halochromic response was observed in water for tetraalkylammonium salts, their thermohalochromic behavior was negligible. A negative halochromic behavior was observed for the dyes in all solvents, when the added cation was Na+. Plots of Δλmaxvs. c (Na+) allowed the apparent association constants for the solvated phenolate-cation pair to be estimated. In most cases, a positive thermohalochromism was observed in the range of 25-50°C, exceptions being the more sterically hindered phenolate dyes in the less polar solvents 2-propanol and acetonitrile. The observed variations were rationalized by invoking the effect of temperature on the phenolate-cation, phenolate-solvent and cation-solvent interactions.

14.
J Mol Model ; 22(9): 218, 2016 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-27553303

RESUMEN

The solvation and the solvatochromic behavior of 5-(dimethylamino)-5'-nitro-2,2'-bithiophene 1, the basis of a π* scale of solvent polarities, was investigated theoretically in toluene, dichloromethane, methanol and formamide with a Monte Carlo and quantum mechanics (QM/MM) iterative approach. The calculated transition energies of the solvatochromic band of 1, obtained as averages of statistically uncorrelated configurations, including the solute and explicit solvent molecules of the first solvation layer, besides showing good agreement with the experimental transitions, reproduced very well the positive solvatochromism of this probe in various solvents.

15.
Magn Reson Chem ; 54(11): 870-873, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27412810

RESUMEN

A series of 4-alkanoyloxy-2,2,6,6-tetramethylpiperidinoxyl radicals was prepared, and their reactivity in water vis-à-vis antioxidant Trolox was compared. Spectral (electron paramagnetic resonance) and dynamic-light-scattering measurements suggested the formation of micelles for the more hydrophobic members of the series. The observed increase in reactivity for the micelle-forming radicals reflected the increased local concentration of the radical fragment on the micellar interface. Copyright © 2016 John Wiley & Sons, Ltd.


Asunto(s)
Óxidos N-Cíclicos/química , Antioxidantes/química , Cromanos/química , Espectroscopía de Resonancia por Spin del Electrón , Radicales Libres/química , Interacciones Hidrofóbicas e Hidrofílicas , Luz , Micelas , Modelos Moleculares , Dispersión de Radiación
16.
Food Chem ; 206: 119-23, 2016 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-27041306

RESUMEN

The activities of two hydrophilic (ascorbic acid and Trolox) and two hydrophobic (α-tocopherol and BHT) antioxidants were measured by reaction with a series of 4-alkanoyloxyTEMPO radical probes 1 in buffered (pH 7), aqueous, micellar solutions of reduced Triton-X 100. In all cases, a cut-off effect was observed, in line with previous observations of the same effect for the partitioning of probe series 1 in this medium. These results support an interpretation of the cut-off effect in food emulsions, based on the "amphiphobic" nature of either the antioxidants or probes: competition between two molecular moieties, for the micellar hydrophobic core, tends to expose a reacting fragment differently to a more hydrophilic microenvironment, as the probe or antioxidant hydrophobicity increases.


Asunto(s)
Antioxidantes/química , Interacciones Hidrofóbicas e Hidrofílicas , Ácido Ascórbico/química , Hidroxitolueno Butilado/química , Cromanos/química , Micelas , Oxidación-Reducción , alfa-Tocoferol/química
17.
Food Chem ; 192: 395-401, 2016 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-26304365

RESUMEN

Partition coefficients for six 4-substituted derivatives of the 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) derivatives in aqueous solutions of reduced Triton X-100 (RTX-100) were determined by measurements of the probe EPR g-factor and of the fluorescence quenching of pyrene by the radical in the micelle. The partition constant attained a maximum value and then decreased with increasing probe hydrophobicity. Simulation of the probes inside the micelle showed that this trend could be rationalized by a change in the orientation of the 4-substituted TEMPO derivatives with the increasing substituent chain-length. The use of the EPR g-factor for the determination of partition constants of radicals in micellar systems was thus validated as a reliable and sensitive method, capable of describing the probe orientation in its microenvironment.


Asunto(s)
Micelas , Simulación de Dinámica Molecular/estadística & datos numéricos , Espectrometría de Fluorescencia/métodos , Fluorescencia , Interacciones Hidrofóbicas e Hidrofílicas
18.
J Mol Model ; 21(8): 212, 2015 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-26224604

RESUMEN

Two variations of the polarized continuum model employing default ("PCM model") and SMD radii ("SMD model") were compared for the reproduction of the solvatochromic behavior of Reichardt's betaine dye, and of eight other phenolate betaines that exhibit a negative, positive or an inverted solvatochromic behavior. Molecules were optimized at the CAM B3LYP/6-31+G(d,p) level of theory, and transition energies were calculated with the TD-DFT method. The PCM model failed to reproduce the negative and the inverted solvachromism of these dyes in protic solvents. The SMD model, though not entirely accounting for hydrogen-bond effects in small, polar hydroxylic solvents, should be recommended as a better alternative for the theoretical simulation of the solvatochromism of phenolate betaines in medium to highly polar solvents. Graphical Abstract A comparison of two polarized continuum models ("default PCM" and "PCM/SMD") for reproducing the solvatochromism of phenolate betaines, with nine examples of negative, positive, and inverted behavior.

19.
J Mol Model ; 21(1): 12, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25617211

RESUMEN

Relative to the corresponding value of phenol, the bond-dissociation energies (BDE) of substituted phenols correlate well with a single descriptor: the Mulliken charge on the oxygen atom of the phenoxyl radical. However, the correlation fails for phenols ortho-substituted with polar groups. Internal reaction coordinates (IRC) for the model reaction of hydrogen abstraction by the hydroperoxyl radical from various 2- and 4-substituted phenols were calculated in order to investigate the role of intra-molecular hydrogen bonds and steric effects on the process. Calculations yielded theoretical values in good agreement with experimental ΔBDE values. The hydrogen-abstraction process was further analyzed in terms of density functional theory (DFT)-based reactivity indices such as local electrophilicity, the Fukui function for nucleophilic attack, and dual descriptor values of the phenolic hydroxyl oxygen along the IRC.

20.
J Mol Model ; 19(2): 689-96, 2013 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23011609

RESUMEN

The solvation and the solvatochromic behavior of the 5-(methylthio)-5'-nitro-2,2'-bithiophene 1 in diethyl ether, dichloromethane, acetonitrile, methanol and formamide was theoretically investigated with an iterative molecular and quantum mechanics (QM/MM) approach. Calculated longest-wavelength solvatochromic absorption band of 1, obtained as averages of statistically uncorrelated configurations, including the solute and explicit solvent molecules of the first and second solvation layer, were in excellent agreement with the experimental results.

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