Search results for "Solvent effects"

showing 10 items of 164 documents

Ionic liquids/[bmim][N3] mixtures: promising media for the synthesis of aryl azides by SNAr

2008

The nucleophilic aromatic substitution of some activated aryl or heteroaryl halides has been performed in ionic liquid solution, using the 1-butyl-3-methylimidazolium azide as a nucleophile. The reaction course was studied varying the structures of both substrates and ionic liquids. In particular, in the latter case, the reaction of 2-bromo-5-nitrothiophene was carried out in five different ionic liquids ([bmim][BF 4], [bmim][PF 6], [bmim][NTf 2], [bm 2im][NTf 2], and [bmpyrr][NTf 2]). Finally, for all the substrates considered, a comparison with data obtained in MeOH solution in the presence of NaN 3 was also performed. Data collected indicate that in some cases it is possible to obtain ar…

ArylOrganic ChemistryMedicinal chemistryionic liquids aril azides task specific ionic liquidschemistry.chemical_compoundchemistryNucleophileNucleophilic aromatic substitutionIonic liquidNucleophilic substitutionOrganic chemistryMoleculeAzideSolvent effects
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1,3-Dipolar cycloadditions of electrophilically activated benzonitrile N-oxides. Polar cycloaddition versus oxime formation.

2006

The reactions of electrophilically activated benzonitrile N-oxides (BNOs) toward 3-methylenephthalimidines (MPIs) have been studied using density functional theory (DFT) at the B3LYP/6-31G* level. For these reactions, two different channels allowing the formation of the [3 + 2] cycloadducts and two isomeric (E)- and (Z)-oximes have been characterized. The 1,3-dipolar cycloadditions take place along concerted but highly asynchronous transition states, while formation of the oximes is achieved through a stepwise mechanism involving zwitterionic intermediates. Both reactions are initiated by the nucleophilic attack of the methylene carbon of the MPIs to the carbon atom of the electrophilically…

Benzonitrilechemistry.chemical_compoundchemistryNucleophileStereochemistryOrganic ChemistrySolvent effectsMethylenePhotochemistryTransition stateCycloadditionElectron localization functionNatural bond orbitalThe Journal of organic chemistry
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DFT calculation of 1J(119Sn,13C) and 2J(119Sn,1H) coupling constants in di- and trimethyltin(IV) compounds

2008

We have tested several computational protocols, at the nonrelativistic DFT level of theory, for the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) spin-spin coupling constants in di- and trimethyltin(IV) derivatives with various ligands. Quite a good agreement with experimental data has been found with several hybrid functionals and a double-zeta basis set for a set of molecules comprising tetra-, penta-, and hexa-coordinated tin(IV). Then, some of the protocols have been applied to the calculation of the 2J(119Sn, 1H) of the aquodimethyltin(IV) ion and dimethyltin(IV) complex with D-ribonic acid and to the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) of the dimethyltin(IV)-glycylglycin…

Carbon Isotopes; Dipeptides; Glycylglycine; Hydrogen; Organotin Compounds; Solvents; Tin; Trimethyltin Compounds; Water; Quantum Theorychemistry.chemical_elementInorganic ChemistryOrganotin(IV) DFT NMR relativistic effects tin couplingsComputational chemistryOrganotin CompoundsMoleculePhysical and Theoretical ChemistryBasis setCoupling constantCarbon IsotopesNMR tin derivatives coupling constantsTrimethyltin CompoundsbiologyGlycylglycineWaterDipeptidesbiology.organism_classificationHybrid functionalSolventchemistryTinSolventsQuantum TheoryTetraSolvent effectsTinHydrogen
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Computer simulation of bottle-brush polymers with flexible backbone: good solvent versus theta solvent conditions.

2011

By Molecular Dynamics simulation of a coarse-grained bead-spring type model for a cylindrical molecular brush with a backbone chain of $N_b$ effective monomers to which with grafting density $\sigma$ side chains with $N$ effective monomers are tethered, several characteristic length scales are studied for variable solvent quality. Side chain lengths are in the range $5 \le N \le 40$, backbone chain lengths are in the range $50 \le N_b \le 200$, and we perform a comparison to results for the bond fluctuation model on the simple cubic lattice (for which much longer chains are accessible, $N_b \le 1027$, and which corresponds to an athermal, very good, solvent). We obtain linear dimensions of …

Chemical Physics (physics.chem-ph)chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceCharacteristic lengthTheta solventFOS: Physical sciencesGeneral Physics and AstronomyBackbone chainPolymerCondensed Matter - Soft Condensed MatterPower lawCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicschemistryChemical physicsPhysics - Chemical PhysicsSide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistrySolvent effectsThe Journal of chemical physics
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A joint action of deep eutectic solvents and ultrasound to promote Diels−Alder reaction in a sustainable way

2020

The need to reduce environmental impact of chemical processes has induced a surge of attention in the choice of solvent and methodologies to carry them out. In this context, we studied the Diels−Alder reaction using N-ethylmaleimide as dienophile and changing the nature of the diene in deep eutectic solvents (DES) under both conventional heating and ultrasonic activation. DES obtained by the combination of different hydrogen bond acceptors and donors allowed assessing the role played by solvent nature. DES proved suitable solvent media for the target reaction, allowing higher yields and faster reactions compared to conventional organic solvents. The trend of yields, both in silent and under…

Chemical processDeep eutectic solventMaterials scienceGeneral Chemical EngineeringContext (language use)02 engineering and technologySolvent effect010402 general chemistry01 natural sciencesRecyclabilityEnvironmental ChemistryUltrasound irradiationEutectic systemDiels–Alder reactionUltrasound irradiationRenewable Energy Sustainability and the EnvironmentfungiGeneral ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesJoint actionDiels−Alder reactionBiochemical engineeringSolvent effects0210 nano-technology
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Ionic liquids: “normal” solvents or nanostructured fluids?

2021

Ionic liquids (ILs) are a class of non-conventional solvents, which, for almost two decades, have continued to generate burgeoning interest in different fields of present-day chemical research with few similar precedents. Among the various aspects related to ILs, a topic worthy of in-depth analysis is their influence on organic reactivity and reaction rates. In light of this, the present short review aims to provide an overview of the literature from 2010 to the present day that addresses this issue. In particular, we herein present two main different viewpoints by which the solvent effect of ILs is explained: the first is mainly based on considering the bulk polarity of ILs and linear solv…

Chemical researchPolymer scienceChemistryPolarity (physics)Organic ChemistrySolvationorganic reactivityLSERSettore CHIM/06 - Chimica OrganicaIonic liquidBiochemistrychemistry.chemical_compoundIonic liquidReactivity (chemistry)Physical and Theoretical ChemistrySolvent effectsSupramolecular catalysis
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Molecular precursors of mesostructured silica materials in the atrane route: A DFT/GIAO/NBO theoretical study

2007

Abstract Quantum chemical calculations using density functional theory have been carried out to investigate two assumed molecular precursors and identified as silatranes (N[OCH2CH2]3Si–OCH2CH2N–(CH2CH2OH)2 and N[OCH2CH2]3Si–OCH2CH2N–(CH2CH2OH)2Na+) which are present in the synthesis of mesoporous silica based material namely “the atrane route”. One of the ways in this synthesis leads to the well-known MCM-41. Additionally, in this work has been also investigated two others molecules such as triethanolamine (TEAH3) and sodatrane which are present in the medium. Gas phase and solution equilibrium geometries of the previous molecules were fully optimized at B3LYP level, modeling solvent effect…

Chemical shiftCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundSolvation shellAtranechemistryComputational chemistryMoleculeDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsBasis setNatural bond orbitalJournal of Molecular Structure: THEOCHEM
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Determination of association constants towards carbon nanotubes

2015

Single-walled carbon nanotubes (SWNTs) are one of the most promising nanomaterials and their supramolecular chemistry has attracted a lot of attention. However, despite well over a decade of research, there is no standard method for the quantification of their noncovalent chemistry in solution/suspension. Here, we describe a simple procedure for the determination of association constants (Ka) between soluble molecules and insoluble and heterogeneous carbon nanotube samples. To test the scope of the method, we report binding constants between five different hosts and two types of SWNTs in four solvents. We have determined numeric values of Ka in the range of 1–104 M−1. Solvent effects as wel…

ChemistryComputational chemistrylawSupramolecular chemistryOrganic chemistryMoleculeGeneral ChemistryCarbon nanotubeSolvent effectsSuspension (chemistry)Nanomaterialslaw.invention
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The Triplet Excimer of Naphthalene: A Model System for Triplet−Triplet Interactions and Its Spectral Properties

2011

Basic concepts of triplet excimer formation and triplet−triplet interactions between molecules with conjugated π-systems are investigated by means of ab initio quantum chemical calculations, employing the second-order coupled-cluster method CC2 and the second-order propagator method ADC(2). The naphthalene dimer turns out to be a very fruitful model system for which weak and strong electronic coupling can be identified depending on the mutual arrangement of the monomer moieties. From geometry optimizations in the excited state, we determine binding energies, including solvent effects, and transient absorption spectra. The most stable T1 conformation turns out to be a face-to-face arrangemen…

ChemistryDimerBinding energyIntermolecular forceAb initioPhotochemistryExcimerSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyChemical physicsExcited statePhysical and Theoretical ChemistrySolvent effectsThe Journal of Physical Chemistry C
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Theoretical Study on the Structures and Electronic Spectra of TCNE2−

2006

Investigations into the charge-separated states and electron-transfer transitions in tetracyanoethylene (TCNE) compiles have recently generated much interest. In this work we present theoretical calculations showing that the most stable structure of the dianion TCNE 2- has D 2d symmetry in vacuum as well as in the solvents dichloromethane and cicetonitrile. By means of the coupled cluster linear response, we compute the vertical electronic spectrum in both the gas phase and solution. The theoreitcal results, are compared to the experimental data and good agreement is achieved.

ChemistryElectronic structureTetracyanoethyleneMolecular physicsAtomic and Molecular Physics and OpticsMolecular electronic transitionSpectral lineSymmetry (physics)chemistry.chemical_compoundCoupled clusterComputational chemistryAb initio quantum chemistry methodsPhysical and Theoretical ChemistrySolvent effectsChemPhysChem
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