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Excess molar volumes of N-methylformamide + tetrahydropyran, + 2-pentanone, + n-propylacetate at the temperatures between 298.15 K and 313.15 K

https://doi.org/10.1016/j.molliq.2006.05.008
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/jcht.1995.0134openalex-snapshot
Excess volumes in (N-methylformamide + methanol + water) at the temperature 313.15K
inferredcites →https://doi.org/10.1006/jcht.1995.0145openalex-snapshot
Excess enthalpies and excess volumes for (butane + ethanol) at the temperatures (298.15, 323.15, and 348.15) K and the pressures (5, 10, and 15) MPa
inferredcites →https://doi.org/10.1016/0021-9614(85)90078-3openalex-snapshot
A thermodynamic study of N-n-butylbenzamide solutions using gas-liquid chromatography
inferredcites →https://doi.org/10.1016/0022-2860(83)90021-2openalex-snapshot
NH…π hydrogen bonding: Infrared study of N-cyclohexylformamide-aromatic donor systems
inferredcites →https://doi.org/10.1016/0022-2860(90)80063-popenalex-snapshot
Hydrogen bonding of N-monosubstituted amides. Ir study of N-butylacetamides
inferredcites →https://doi.org/10.1016/j.molliq.2004.12.001openalex-snapshot
Excess molar volumes of N-methylacetamide+tetrahydrofuran, +2-butanone, +ethylacetate at the temperatures between 303.15 K and 318.15 K
inferredcites →https://doi.org/10.1016/j.molliq.2005.09.008openalex-snapshot
Excess molar volumes of N-methylformamide+tetrahydrofuran, +2-butanone, +ethylacetate at the temperatures between 303.15 K and 318.15 K
inferredcites →https://doi.org/10.1016/s0021-9614(03)00053-3openalex-snapshot
Excess molar volumes of tetrahydrofuran or tetrahydrothiophene+an alkyne at K
inferredcites →https://doi.org/10.1016/s0022-2860(96)09544-0openalex-snapshot
NH…π hydrogen bonding: FTIR study of N-butylpropionamides-aromatic donor systems
inferredcites →https://doi.org/10.1016/s0167-7322(01)00265-3openalex-snapshot
Excess molar volumes of 1-propanol + formamide, + N-methylformamide, + N,N-dimethylformamide at 303.15 K
inferredcites →https://doi.org/10.1016/s0378-3812(02)00042-0openalex-snapshot
Application of the ERAS-Model to binary mixtures of diethylamine and s-butylamine with acetonitrile in the temperature range (288.15–303.15) K
inferredcites →https://doi.org/10.1021/ie50458a036openalex-snapshot
Algebraic Representation of Thermodynamic Properties and the Classification of Solutions
inferredcites →https://doi.org/10.1021/j100231a022openalex-snapshot
Dielectric properties and molecular structure of amide solutions. 1. N-Methylacetamide in carbon tetrachloride
inferredcites →https://doi.org/10.1021/j100676a010openalex-snapshot
Chain association equilibriums. Nuclear magnetic resonance study of the hydrogen bonding of N-monosubstituted amines. III. In dioxane
inferredcites →https://doi.org/10.1021/j100785a011openalex-snapshot
Dielectric Properties of Alkyl Amides. II. Liquid Dielectric Constant and Loss
inferredcites →https://doi.org/10.1021/j100803a016openalex-snapshot
DIELECTRIC CONSTANT OF HYDROGEN-BONDED LIQUIDS. II. N-MONOSUBSTITUTED ACETAMIDES
inferredcites →https://doi.org/10.1021/j100889a008openalex-snapshot
Chain Association Equilibria. A Nuclear Magnetic Resonance Study of the Hydrogen Bonding of N-Monosubstituted Amides1a
inferredcites →https://doi.org/10.1021/j150560a010openalex-snapshot
Dielectric Constants and Viscosities of Several N-Substituted Amides as Functions of their Structure and of Temperature
inferredcites →https://doi.org/10.1021/ja00877a009openalex-snapshot
Hydrogen Bonds between Model Peptide Groups in Solution
inferredcites →https://doi.org/10.1021/je00008a024openalex-snapshot
Viscosities and densities for propylene carbonate + toluene at 15, 20, 25, 30, and 35.degree.C
inferredcites →https://doi.org/10.1021/je00015a052openalex-snapshot
Infinite Dilution Activity Coefficients of Organic Solutes in N,N-Diethyldodecanamide
inferredcites →https://doi.org/10.1071/ch9700967openalex-snapshot
Volumes of mixing and viscosities of liquid mixtures of ketones and o-chlorophenol
inferredcites →https://doi.org/10.1351/pac198658121677openalex-snapshot
Atomic weights of the elements 1985
inferredcites →https://doi.org/10.1515/zpch-1974-255112openalex-snapshot
Studien zur Thermodynamik binärer Flüssigkeitsgemische mit homologen Formamiden
inferredcites →https://doi.org/10.1524/zpch.1972.81.5_6.330openalex-snapshot
Estimation of Molecular Interaction Energies in some Amides1

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4494446openalex-extracted
Acoustic and Volumetric Study of Binary Mixtures Containing Ethyl Propionate with Amides at Various Temperatures
inferred← citeshttps://doi.org/10.1007/s10953-013-9991-zopenalex-snapshot
Molecular Interactions in 1-Ethyl-3-Methylimidazolim Tetrafluoroborate + Amide Mixtures: Excess Molar Volumes, Excess Isentropic Compressibilities and Excess Molar Enthalpies
inferred← citeshttps://doi.org/10.1007/s10953-015-0358-5openalex-snapshot
Topological Investigations of Excess Heat Capacities of Binary and Ternary Liquid Mixtures Containing o-Chlorotoluene, Amides and Cyclohexane at 298.15, 303.15 and 308.15 K
inferred← citeshttps://doi.org/10.1007/s10973-018-7032-2openalex-snapshot
Excess heat capacities and excess molar enthalpies of the mixtures containing tetrahydropyran, piperidine and cyclic alkanones
inferred← citeshttps://doi.org/10.1016/j.fluid.2016.08.014openalex-snapshot
PρT measurement and PC-SAFT modeling of N,N-dimethyl formamide, N -methyl formamide, N,N-dimethyl acetamide, and ethylenediamine from T = (293.15–423.15) K and pressures up to 35 MPa
inferred← citeshttps://doi.org/10.1016/j.jct.2014.06.030openalex-snapshot
Excess molar volumes and excess isentropic compressibilities of binary and ternary mixtures of o-chlorotoluene with cyclic ether and amides or cyclohexane at different temperatures
inferred← citeshttps://doi.org/10.1016/j.jct.2023.107222openalex-snapshot
Acoustic and volumetric study of binary mixtures containing Ethyl propionate with amides at various temperatures
inferred← citeshttps://doi.org/10.1016/j.jct.2025.107616openalex-snapshot
Thermophysical properties and FTIR spectral investigation of intermolecular interactions in binary mixtures of N-methylformamide with polyethylene glycols at temperatures from 293.15 to 323.15 K: Experimental results and theoretical modeling
inferred← citeshttps://doi.org/10.1016/j.jct.2026.107717openalex-snapshot
Volumetric, acoustic, viscometric and FTIR studies of molecular interactions in N-methylformamide + alkyl acetates (methyl, ethyl, n-propyl, and n-butyl) binary mixtures at temperatures from 293.15 to 323.15 K: Experimental and theoretical approach
inferred← citeshttps://doi.org/10.1016/j.molliq.2013.11.016openalex-snapshot
Densitometric and spectroscopic investigation of interactions of selected N-substituted amides and acetonitrile
inferred← citeshttps://doi.org/10.1016/j.molliq.2013.12.039openalex-snapshot
Volumetric properties of ammonium nitrate in N-methylformamide
inferred← citeshttps://doi.org/10.1016/j.molliq.2016.07.060openalex-snapshot
Study of molecular interactions in binary liquid mixtures containing tri-n-butylamine with 2-pentanone, 3-pentanone, and 4-methyl-2-pentanone: A thermophysical approach
inferred← citeshttps://doi.org/10.1016/j.molliq.2017.10.007openalex-snapshot
Thermodynamics of amide + ketone mixtures. 2. Volumetric, speed of sound and refractive index data for N,N-dimethylacetamide + 2-alkanone systems at several temperatures. Application of Flory's model to tertiary amide +n-alkanone systems
inferred← citeshttps://doi.org/10.1016/j.molliq.2017.12.083openalex-snapshot
Excess molar volumes and excess isentropic compressibilities of liquid mixtures formed by tetrahydropyran, piperidine and cyclic ketones at temperature from 293.15 to 308.15 K.
inferred← citeshttps://doi.org/10.1016/j.molliq.2021.115646openalex-snapshot
PVT properties of binary systems of diisopropylethylammonium octanoate ionic liquid with oligomeric polyethylene glycol or polypropylene glycol at elevated pressures
inferred← citeshttps://doi.org/10.1016/j.molstruc.2008.02.016openalex-snapshot
N–H...O hydrogen bonding. FT-IR, NIR and 1H NMR study of N-methylpropionamide – Dialkyl ether systems
inferred← citeshttps://doi.org/10.1016/j.molstruc.2012.10.009openalex-snapshot
FTIR spectroscopic study of hydrogen bonding and solvent induced frequency shifts of N-tert-butylacetamide
inferred← citeshttps://doi.org/10.1016/j.tca.2011.06.020openalex-snapshot
Topological investigations of molecular interactions of binary and ternary mixtures containing tetrahydropyran, o-toluidine and N-methylformamide
inferred← citeshttps://doi.org/10.1021/acs.jced.6b00606openalex-snapshot
Thermodynamic Studies of Molecular Interactions in Mixtures Containing Tetrahydropyran, 1,4-Dioxane, and Cyclic Ketones
inferred← citeshttps://doi.org/10.1021/acs.jced.8b00547openalex-snapshot
Density, Speed of Sound, and Refractive Index Measurements for Binary Mixtures of Pentan-2-one with Propan-2-ol and Butan-2-ol
inferred← citeshttps://doi.org/10.1021/acs.jced.9b01070openalex-snapshot
Density, Speed of Sound, and Refractive Index Measurements for Mixtures of n-Heptane with Pentan-2-one or 4-Methylpentan-2-one for T = 298.15–338.15 K and 0.101 MPa
inferred← citeshttps://doi.org/10.1021/je300941vopenalex-snapshot
Volumetric Properties of Binary Mixtures of 1-Butyl-1-methylpyrrolidinium Bis(trifluoromethylsulfonyl)imide with N-Methylformamide and N,N-Dimethylformamide from (293.15 to 323.15) K
inferred← citeshttps://doi.org/10.1021/je300974gopenalex-snapshot
Volumetric Properties of Binary Mixtures of N-Ethylformamide with Tetrahydropyran, 2-Pentanone, and Propylacetate from (293.15 to 313.15) K
inferred← citeshttps://doi.org/10.1021/je400722hopenalex-snapshot
Densities, Speeds of Sound, Excess Molar Enthalpies, and Heat Capacities of o-Chlorotoluene and Cyclic Ether Mixtures
inferred← citeshttps://doi.org/10.1021/je400803fopenalex-snapshot
Volumetric Properties of Binary Mixtures of 1-Butyl-1-Methylpyrrolidinium Tris(pentafluoroethyl)trifluorophosphate with N-Methylformamide, N-Ethylformamide, N,N-Dimethylformamide, N,N-Dibutylformamide, and N,N-Dimethylacetamide from (293.15 to 323.15) K
inferred← citeshttps://doi.org/10.1021/je5002945openalex-snapshot
Volumetric Properties of Binary Mixtures of 1-Butyl-3-Methylimidazolium Tris(pentafluoroethyl)trifluorophosphate with N-Methylformamide, N-Ethylformamide, N,N-Dimethylformamide, N,N-Dibutylformamide, and N,N-Dimethylacetamide from (293.15 to 323.15) K
inferred← citeshttps://doi.org/10.2298/jsc1002157jopenalex-snapshot
N-H···O hydrogen bonding: An FT-IR, NIR study of N-methylformamide-ether systems
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