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Proton Transfer Equilibria in Schiff Bases with Steric Repulsion

https://doi.org/10.1021/jp035009c
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What this work says

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

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Proton transfer reaction in N‐methyl‐2‐hydroxy‐Schiff bases
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FTIR study of the protonation of a schiff base in chloroform-methanol mixtures
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The influence of steric effects of proton-transfer equilibrium in intramolecular hydrogen bonds
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Protonation and hydrogen bonding by polyenic Schiff bases
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Deuterium isotope effect on 13C NMR spectra of ortho Mannich bases
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Physico-chemical properties of coordinating compounds—IV
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The influence of the fluorosubstituence on the intensity of CN valence vibrations in aromatic Schiff bases
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Integrated intensity of OH absorption bands in bent hydrogen bonds in ortho-dialkylaminomethyl phenols
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Photochromism and proton transfer reaction cycle of new internally H-bonded Schiff bases
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Dipole moments and conformation of Schiff bases with intramolecular hydrogen bonds
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Strengthening of the intramolecular O⋯H⋯N hydrogen bonds in Schiff bases as a result of steric repulsion
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Specificity of the intramolecular hydrogen bond. The differences in spectroscopic characteristics of the intermolecular and intramolecular H-bonds
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Low temperature studies on ultraviolet and infrared spectra of ortho Mannich bases
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Steady-State and Time-Resolved Study of the Proton-Transfer Fluorescence of 4-Hydroxy-5-azaphenanthrene in Model Solvents and in Complexes with Human Serum Albumin
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Effect of acids on the infrared spectra of the Schiff base of trans-retinal
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Solvent effect on the intramolecular hydrogen bond strength and on the isotopic ratio .nu.NH+/.nu.ND+ in a trisubstituted Mannich base
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Spectroscopic studies of the photochromic molecule N-(2-hydroxybenzylidene)aniline and its photoproduct
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Infrared spectra of N-aryl imines of o-hydroxybenzaldehyde between 2000 and 1500 cm-1
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Evidence for resonance-assisted hydrogen bonding from crystal-structure correlations on the enol form of the .beta.-diketone fragment
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Rehybridization of the carbon-nitrogen double bond upon protonation of methylimine increases its stretching force constant
inferredcites →https://doi.org/10.1021/ja00968a024openalex-snapshot
Kinetics of Hydrolysis of Hydroxy and Methoxy Derivatives of N-Benzylidene-2-aminopropane
inferredcites →https://doi.org/10.1021/ja982161xopenalex-snapshot
Competition between Rotamerization and Proton Transfer in o-Hydroxybenzaldehyde
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Theoretical Studies of Excited State Proton Transfer in Small Model Systems
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Vibrational Analysis of a Schiff Base Based on ab Initio Molecular Orbital Calculations: Effect of Electron Correlation on the CN Stretching Force Constant and the Origin of the Shift of the CN Stretching Frequency upon Protonation and Hydrogen-Bond Formation
inferredcites →https://doi.org/10.1021/jp961115lopenalex-snapshot
Solvatochromism in N-(2-Hydroxybenzylidene)aniline, N-(2-Hydroxybenzylidene)benzylamine, and N-(2-Hydroxybenzylidene)-2-phenylethylamine
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Factors That Influence the CN Stretching Frequency in Imines
inferredcites →https://doi.org/10.1021/jp970814aopenalex-snapshot
Through-Resonance Assisted Ionic Hydrogen Bonding in 5-Nitro-N-salicylideneethylamine
inferredcites →https://doi.org/10.1039/f19817702309openalex-snapshot
Thermodynamic parameters for the proton-transfer reaction in mannich bases
inferredcites →https://doi.org/10.1063/1.1316038openalex-snapshot
Theoretical approach to photochromism of aromatic Schiff bases: A minimal chromophore salicylidene methylamine
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Photochromism of salicylideneaniline (SA). How the photochromic transient is created: A theoretical approach
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Hydrogen Bonding
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A spectroscopic study of the solvent dependent processes of the anils of benzaldehyde and salicylaldehyde
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Einführung in die theoretische organische Chemie.
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Specific Features of Intramolecular Proton Transfer Reaction in Schiff Bases
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An introduction to hydrogen bonding

What points at this work

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