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Calorimetric studies on some hydrogen-bonded adducts

https://doi.org/10.1021/ja00999a006
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inferred← citeshttps://doi.org/10.2139/ssrn.4892996openalex-extracted
Can the hydrogen bonding enthalpy be calculated from the binding constant at 298.15 K?
inferred← citeshttps://doi.org/10.1002/(sici)1099-1395(199605)9:5<241::aid-poc782>3.0.co;2-copenalex-snapshot
Hydrogen bonding in pure base media. Correlations between calorimetric and infrared spectroscopic data
inferred← citeshttps://doi.org/10.1002/9780470171875.ch1openalex-snapshot
A Critical Evaluation of the Concept of Fluorine Hyperconjugation
inferred← citeshttps://doi.org/10.1002/9780470771242.ch3openalex-snapshot
Basicity, hydrogen bonding and complex formation
inferred← citeshttps://doi.org/10.1002/9783527834914.ch12openalex-snapshot
IR and NMR Spectral Diagnostics of Hydrogen Bond Energy and Geometry
inferred← citeshttps://doi.org/10.1002/app.21510openalex-snapshot
Adsorption from aqueous solution based on the synergism between hydrogen bonding and hydrophobic interactions
inferred← citeshttps://doi.org/10.1002/bscb.19830920401openalex-snapshot
The Conformation and Charge Distribution in the Hydrogen Bonded Chelate Ring of Mannich Bases
inferred← citeshttps://doi.org/10.1002/ejoc.200400311openalex-snapshot
Empirical Treatment of the Inductive and Dispersive Components of Solute−Solvent Interactions: The Solvent Polarizability (SP) Scale
inferred← citeshttps://doi.org/10.1002/jlac.199519950234openalex-snapshot
Progress towards a generalized solvent polarity scale: The solvatochromism of 2‐(dimethylamino)‐7‐nitrofluorene and its homomorph 2‐fluoro‐7‐nitrofluorene
inferred← citeshttps://doi.org/10.1002/jlac.199619961112openalex-snapshot
A Generalized Solvent Basicity Scale: The Solvatochromism of 5‐Nitroindoline and Its Homomorph 1‐Methyl‐5‐nitroindoline
inferred← citeshttps://doi.org/10.1002/jlac.199719970921openalex-snapshot
A Generalized Solvent Acidity Scale: The Solvatochromism of o‐tert‐Butylstilbazolium Betaine Dye and Its Homomorph o,o′‐Di‐tert‐butylstilbazolium Betaine Dye
inferred← citeshttps://doi.org/10.1002/jrs.2003openalex-snapshot
Investigating the formation of an adduct of formamide with dioxane by means of Raman spectroscopy
inferred← citeshttps://doi.org/10.1002/mrc.1260311004openalex-snapshot
Variable‐temperature NMR studies of 2,6‐dihydroxy acylaromatic compounds. Deuterium isotope effects on chemical shifts, isotopic perturbation of equilibrium and barriers to rotation
inferred← citeshttps://doi.org/10.1002/poc.437openalex-snapshot
An enthalpic scale of hydrogen‐bond basicity, part 1: halogenoalkanes
inferred← citeshttps://doi.org/10.1002/pola.1988.080260320openalex-snapshot
Interchain electron donor–acceptor complexes. Determination of equilibrium constant and thermodynamic parameters in the solid state
inferred← citeshttps://doi.org/10.1002/polb.1986.090240716openalex-snapshot
Hydrogen bonding in polymer mixtures
inferred← citeshttps://doi.org/10.1002/polb.1995.090331309openalex-snapshot
Intermolecular interactions in substituted phenols. Investigation of model compounds
inferred← citeshttps://doi.org/10.1002/prac.19703120510openalex-snapshot
Struktur‐Reaktivitätsuntersuchungen mit heterosubstituierten Nitrilen. II. H‐Brückenwechselwirkungen zwischen OH‐Protonendonatoren und Cyanverbindungen Korrelationen
inferred← citeshttps://doi.org/10.1002/recl.19700890709openalex-snapshot
Hydrogen bonding properties of α‐Diazosulfones and α‐Diazoketones
inferred← citeshttps://doi.org/10.1002/recl.19710900609openalex-snapshot
Hydrogen bonding. Part IV: The ground state basicities of N,N‐disubstituted sulfinamides and sulfonamides
inferred← citeshttps://doi.org/10.1002/recl.19710901204openalex-snapshot
Hindered internal rotation in carbamates: An NMR study of the conformations of alkyl and arylN‐(alkylsulfonylmethyl)‐N‐methylcarbamates and arylN‐(arylsulfonylmethyl)‐N‐methylcarbamates
inferred← citeshttps://doi.org/10.1002/zfch.19750151002openalex-snapshot
Schwache Elektronen‐Donator‐Akzeptor‐Komplexe — Fortschritte und Probleme
inferred← citeshttps://doi.org/10.1002/zfch.19750151102openalex-snapshot
Neuere Erkenntnisse über die Natur und Eigenschaften der Wasserstoffbrückenbindung
inferred← citeshttps://doi.org/10.1007/978-1-4684-1959-7_4openalex-snapshot
Spectroscopic Measurements
inferred← citeshttps://doi.org/10.1007/978-1-4684-2049-4_6openalex-snapshot
Sulfides
inferred← citeshttps://doi.org/10.1007/978-1-4684-8471-7_4openalex-snapshot
The Vibrational Spectra of Hydrogen-Bonded Complexes
inferred← citeshttps://doi.org/10.1007/978-1-4684-8589-9_6openalex-snapshot
Spectroscopic Studies of Hydrogen Bonding
inferred← citeshttps://doi.org/10.1007/978-1-4757-4509-2_20openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-009-6312-2_13openalex-snapshot
Measurement of Complexing Constants and Enthalpies of Complexing by Batch Calorimetry
inferred← citeshttps://doi.org/10.1007/bf00607982openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00610539openalex-snapshot
The IR spectra and proton-accepting capacity of the carbonyl group in dicarboxylic acid derivatives
inferred← citeshttps://doi.org/10.1007/bf00613644openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00743851openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00920885openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00973210openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00973782openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bfb0036784openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0001-8716(75)80023-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0009-2614(90)80103-kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0009-2614(95)00912-nopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0022-1902(74)80059-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0022-2852(69)90140-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0022-2860(71)87080-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0022-2860(78)87013-6openalex-snapshot
The phenol-pyridine hydrogen bonded complex: a cndo/2 study
inferred← citeshttps://doi.org/10.1016/0022-2860(80)85166-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0032-3950(81)90203-3openalex-snapshot
The mechanism of amide catalysis of the reaction of the formation of polyimides
inferred← citeshttps://doi.org/10.1016/0040-4020(76)80102-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0040-4020(82)85105-3openalex-snapshot
An infrared study of hydrogen-bonding between phenols and sulphoxides
inferred← citeshttps://doi.org/10.1016/0040-6031(73)87011-xopenalex-snapshot
Calorimetric investigations of association equilibria: the pyridine-iodine complex in cyclohexane and in carbon tetrachloride
inferred← citeshttps://doi.org/10.1016/0040-6031(74)87017-6openalex-snapshot
Complexes moléculaires de faible stabilité détermination des constantes de formation par les méthodes d'analyse linéaire. Étude critique des conditions expérimentales et de la gamme de constantes accessible
inferred← citeshttps://doi.org/10.1016/0040-6031(89)87160-6openalex-snapshot
Critical review of the calorimetric method for equilibrium constant determination
inferred← citeshttps://doi.org/10.1016/0043-1354(73)90008-0openalex-snapshot
Organic desorption from carbon—II. The effect of solvent in the desorption of phenol from wet carbon
inferred← citeshttps://doi.org/10.1016/0043-1354(73)90009-2openalex-snapshot
Organic desorption from carbon—III. The effect of solvent in the desorption of phenol from dry carbon
inferred← citeshttps://doi.org/10.1016/0167-7322(92)80104-popenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0378-3812(85)90027-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0378-4487(77)80037-xopenalex-snapshot
Theoretical study of the hydrogen bonding ability of phenol and its ortho, meta and para substituted derivatives
inferred← citeshttps://doi.org/10.1016/0584-8539(68)80221-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0584-8539(69)80086-3openalex-snapshot
The association of 2,6-di-t-butylphenol
inferred← citeshttps://doi.org/10.1016/0584-8539(69)80147-9openalex-snapshot
Comparative NMR and infrared measurements of relatively small association equilibrium constants; interaction of phenol with alkyl halides: tri-n-butyl amine and phosphine
inferred← citeshttps://doi.org/10.1016/0584-8539(69)80168-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0584-8539(70)80079-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0584-8539(74)80028-0openalex-snapshot
Hydrogen bonds between co-ordinated BH3 and BH2 groups and OH groups. Thermodynamics of formation by infrared spectroscopy
inferred← citeshttps://doi.org/10.1016/0584-8539(74)80039-5openalex-snapshot
Hydrogen bonding—V. Inductive effects on the ground state basicity of sulfones. The electronegativity of a covalently bound perchlorate group
inferred← citeshttps://doi.org/10.1016/b978-0-12-433805-0.50008-2openalex-snapshot
Solvent Basicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-580201-7.50010-2openalex-snapshot
SPECTROSCOPY OF DONOR–ACCEPTOR SYSTEMS
inferred← citeshttps://doi.org/10.1016/b978-0-444-99697-8.50010-1openalex-snapshot
Experimental Methods Employed in the Study of Non-Aqueous Solutions if Complex Systems
inferred← citeshttps://doi.org/10.1016/b978-1-77467-040-8.50012-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-1-895198-64-5.50016-7openalex-snapshot
SOLVENT EFFECTS BASED ON PURE SOLVENT SCALES
inferred← citeshttps://doi.org/10.1016/b978-1-927885-38-3.50011-5openalex-snapshot
ACID-BASE AND OTHER INTERACTIONS
inferred← citeshttps://doi.org/10.1016/j.molliq.2006.02.005openalex-snapshot
The concept of associated solutions in historical development. Part 1. The 1884–1984 period
inferred← citeshttps://doi.org/10.1016/j.molliq.2006.09.001openalex-snapshot
Erratum to “The concept of associated solutions in historical development: Part 1. The 1884–1984 period” [J. Mol. Liq. 128 (2006) 1–31]
inferred← citeshttps://doi.org/10.1016/j.molliq.2016.12.033openalex-snapshot
Polarizability over dipolarity for the spectroscopic behavior of azobenzenes in room-temperature ionic liquids and organic solvents
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120765openalex-snapshot
The comparative analysis of solvation thermochemistry of organic non-electrolytes in ionic liquids and molecular solvents
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125353openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.vibspec.2010.04.010openalex-snapshot
Formamide complexes with selected azabenzenes: A discussion on their thermodynamic properties from Raman analyses
inferred← citeshttps://doi.org/10.1016/s0166-1280(98)00292-9openalex-snapshot
Post-Hartree–Fock study on biologically important di- and tripyrrolic compounds—precursors to the active site of phytochrome
inferred← citeshttps://doi.org/10.1016/s0167-2991(04)80011-9openalex-snapshot
Microbial Depolymerization of Coal
inferred← citeshttps://doi.org/10.1016/s0167-2991(13)65468-3openalex-snapshot
References
inferred← citeshttps://doi.org/10.1016/s1386-1425(96)01818-5openalex-snapshot
Spectroscopic and thermodynamic properties of hydrogen bonded water molecules in binary liquid mixtures
inferred← citeshttps://doi.org/10.1016/s1386-1425(98)00348-5openalex-snapshot
Direct proportionality of the hydrogen bonding energy and the intensification of the stretching ν(XH) vibration in infrared spectra
inferred← citeshttps://doi.org/10.1021/ac60267a006openalex-snapshot
Theoretical evaluation of entropy titration method for calorimetric determination of equilibrium constants in aqueous solution
inferred← citeshttps://doi.org/10.1021/ac60338a035openalex-snapshot
Molecular interactions of asphalt. Infrared study of the hydrogen-bonding basicity of asphalt
inferred← citeshttps://doi.org/10.1021/ac60351a037openalex-snapshot
Quantitative method using differential infrared spectrometry for the determination of compound types absorbing in the carbonyl region in asphalts
inferred← citeshttps://doi.org/10.1021/acs.jpca.8b00541openalex-snapshot
Hybridization of Nitrogen Determines Hydrogen-Bond Acceptor Strength: Gas-Phase Comparison of Redshifts and Equilibrium Constants
inferred← citeshttps://doi.org/10.1021/acsapm.1c00501openalex-snapshot
Rheology of Polytriazole/ZIF-8 Solutions and Dynamics of Mixed-Matrix Composite Films
inferred← citeshttps://doi.org/10.1021/acssuschemeng.8b04451openalex-snapshot
Lignosulfonate/Dicationic Ionic Liquid Composite as a Task-Specific Catalyst Support for Enabling Efficient Synthesis of Unsymmetrical 1,3-Diynes with A Low Substrate Ratio
inferred← citeshttps://doi.org/10.1021/bi00415a007openalex-snapshot
Tyrosine hydrogen-bonding and environmental effects in proteins probed by ultraviolet resonance Raman spectroscopy
inferred← citeshttps://doi.org/10.1021/ef0001787openalex-snapshot
Estimation of Hydrogen Bond Distribution in Coal through the Analysis of OH Stretching Bands in Diffuse Reflectance Infrared Spectrum Measured by in-Situ Technique
inferred← citeshttps://doi.org/10.1021/jo050535gopenalex-snapshot
An Enthalpic Scale of Hydrogen-Bond Basicity. 3. Ammonia, Primary, Secondary, and Tertiary Amines
inferred← citeshttps://doi.org/10.1021/jo9614248openalex-snapshot
Solvent Effects on a Diels−Alder Reaction Involving a Cationic Diene: Consequences of the Absence of Hydrogen-Bond Interactions for Accelerations in Aqueous Media
inferred← citeshttps://doi.org/10.1021/jo9901485openalex-snapshot
Poly Methoxy Phenols in Solution: O−H Bond Dissociation Enthalpies, Structures, and Hydrogen Bonding
inferred← citeshttps://doi.org/10.1021/jp0581781openalex-snapshot
Pentachlorocyclopropane/Base Complexes: Matrix Isolation Infrared Spectroscopic and Density Functional Study of C−H- - -N Hydrogen Bonds
inferred← citeshttps://doi.org/10.1021/jp8095727openalex-snapshot
Toward a Generalized Treatment of the Solvent Effect Based on Four Empirical Scales: Dipolarity (SdP, a New Scale), Polarizability (SP), Acidity (SA), and Basicity (SB) of the Medium
inferred← citeshttps://doi.org/10.1021/jp970239aopenalex-snapshot
On Solvent Basicity: Analysis of the SB Scale
inferred← citeshttps://doi.org/10.1021/la990091hopenalex-snapshot
Correlation between Adsorption and Small Molecule Hydrogen Bonding
inferred← citeshttps://doi.org/10.1039/b921003bopenalex-snapshot
Hydrogen bonding properties of non-polar solvents
inferred← citeshttps://doi.org/10.1039/c6py01401aopenalex-snapshot
Artificial membranes with selective nanochannels for protein transport
inferred← citeshttps://doi.org/10.1039/d0cp01589jopenalex-snapshot
O–H stretching frequency red shifts do not correlate with the dissociation energies in the dimethylether and dimethylsulfide complexes of phenol derivatives
inferred← citeshttps://doi.org/10.1039/d5cp02393aopenalex-snapshot
Hydrogen bonding and van der Waals forces contributions to the melting enthalpy: insights from volumetric and spectroscopic data
inferred← citeshttps://doi.org/10.1039/d6cp00710dopenalex-snapshot
Correlating NMR H/D exchange kinetics with IR red shifts: towards a comprehensive scale for intermolecular hydrogen bond strength
inferred← citeshttps://doi.org/10.1039/p29920001827openalex-snapshot
A unified scale for understanding and predicting non-specific solvent polarity: a dynamic cavity model
inferred← citeshttps://doi.org/10.1063/1.462009openalex-snapshot
Rotational coherence spectroscopy and structure of phenol dimer
inferred← citeshttps://doi.org/10.1063/1.468678openalex-snapshot
Proton transfer in hydrogen-bonded acid–base complexes in polar solvents
inferred← citeshttps://doi.org/10.1063/5.0263484openalex-snapshot
Extending Badger’s rule. II. The relationship between energy and vibrational spectra in hydrogen bonds
inferred← citeshttps://doi.org/10.1080/01496399008051841openalex-snapshot
Selective Adsorption of Solutes Based on Hydrogen Bonding
inferred← citeshttps://doi.org/10.1080/05704926808050887openalex-snapshot
Spectroscopic Studies of the Hydrogen Bond
inferred← citeshttps://doi.org/10.1134/s0022476617030180openalex-snapshot
Weak hydrogen bonds in adsorption of nonrigid molecules on graphitized thermal carbon black
inferred← citeshttps://doi.org/10.1134/s1070363207020120openalex-snapshot
Solvatochromism of heteroaromatic compounds: XXXI. Energetics of hydrogen bonding between N-methyltrifluoromethanesulfonamide and ethers
inferred← citeshttps://doi.org/10.1142/s0217984914300142openalex-snapshot
A brief review of Badger–Bauer rule and its validation from a first-principles approach
inferred← citeshttps://doi.org/10.1246/bcsj.44.923openalex-snapshot
An Infrared Spectroscopic Study of Hydrogen Bonds. The Liquid-Liquid Interaction of Solvents with Trimethylsilanol
inferred← citeshttps://doi.org/10.1246/bcsj.47.871openalex-snapshot
A Study of the Interaction of Diethylcadmium with Lewis Bases as Solvents
inferred← citeshttps://doi.org/10.3389/fchem.2023.1176746openalex-snapshot
Solvent and solvation effects on reactivities and mechanisms of phospho group transfers from phosphate and phosphinate esters to nucleophiles
inferred← citeshttps://doi.org/10.3390/liquids4030034openalex-snapshot
Calculation of Hydrogen Bonding Enthalpy Using the Two-Parameter Abraham Equation
inferred← citeshttps://doi.org/10.3390/liquids4040037openalex-snapshot
Quantum Chemical (QC) Calculations and Linear Solvation Energy Relationships (LSER): Hydrogen-Bonding Calculations with New QC-LSER Molecular Descriptors
inferred← citeshttps://doi.org/10.3390/molecules25235512openalex-snapshot
A Critical Overview of Current Theoretical Methods of Estimating the Energy of Intramolecular Interactions
inferred← citeshttps://doi.org/10.3390/molecules27134082openalex-snapshot
Fast Quantum Approach for Evaluating the Energy of Non-Covalent Interactions in Molecular Crystals: The Case Study of Intermolecular H-Bonds in Crystalline Peroxosolvates
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