Reference health
A step towards the a priori design of ionic liquids
47/47 checkable references clean · checked 2026-07-24
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
The 47 checked references that resolve
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The solvatochromic comparison method. I. The .beta.-scale of solvent hydrogen-bond acceptor (HBA) basicities
resolves10.1021/ja00426a036
The solvatochromic comparison method. 2. The .alpha.-scale of solvent hydrogen-bond donor (HBD) acidities
resolves10.1021/ja00460a031
The solvatochromic comparison method. 6. The .pi.* scale of solvent polarities
resolves10.1039/cs9932200073
Scales of solute hydrogen-bonding: their construction and application to physicochemical and biochemical processes
resolves10.1080/00319100801993407
Computation methodology for determining Abraham solute descriptors from limited experimental data by combining Abraham model and Goss-modified Abraham model correlations
resolves10.1021/ja01045a038
Studies of hydrogen-bonded complex formation with p-fluorophenol. V. Linear free energy relationships with OH reference acids
resolves10.1021/ja01045a037
Studies of hydrogen-bonded complex formation with p-fluorophenol. IV. Fluorine nuclear magnetic resonance method
resolves10.1021/jo100461z
An Enthalpic Scale of Hydrogen-Bond Basicity. 4. Carbon π Bases, Oxygen Bases, and Miscellaneous Second-Row, Third-Row, and Fourth-Row Bases and a Survey of the 4-Fluorophenol Affinity Scale
resolves10.1080/10629360903278701
Thermodynamics of organic chemical hydration: QSPR models using physicochemical HYBOT descriptors
resolves10.1021/ja028156h
Characterizing Ionic Liquids On the Basis of Multiple Solvation Interactions
resolves10.1021/jo0615302
Using Kamlet−Taft Solvent Descriptors To Explain the Reactivity of Anionic Nucleophiles in Ionic Liquids
resolves10.1021/ie070632v
Nucleophilic Reactions at Cationic Centers in Ionic Liquids and Molecular Solvents
resolves10.1039/b920651p
A COSMO-RS based guide to analyze/quantify the polarity of ionic liquids and their mixtures with organic cosolvents
resolves10.1039/p29890000699
Hydrogen bonding. Part 7. A scale of solute hydrogen-bond acidity based on log K values for complexation in tetrachloromethane
resolves10.1039/p29900000521
Hydrogen bonding. Part 10. A scale of solute hydrogen-bond basicity using log K values for complexation in tetrachloromethane
resolves10.1021/jp076895k
Solvent Polarities and Kamlet−Taft Parameters for Ionic Liquids Containing a Pyridinium Cation
resolves10.1016/0009-2614(93)85547-2
Computing molecular electrostatic potentials with the PRISM algorithm
resolves10.1002/chem.200600103
Characterising the Electronic Structure of Ionic Liquids: An Examination of the 1‐Butyl‐3‐Methylimidazolium Chloride Ion Pair
resolves10.1016/S0166-1280(01)00634-0
A CIS study of solvent effects on the electronic absorption spectrum of Reichardt's dye
resolves10.1021/jp0547865
Structural Characterization of the 1-Butyl-3-methylimidazolium Chloride Ion Pair Using ab Initio Methods
resolves10.1021/jp8107649
Ion-Pair Binding Energies of Ionic Liquids: Can DFT Compete with Ab Initio-Based Methods?
resolves10.1039/c0cc05223j
Reaction of elemental chalcogens with imidazolium acetates to yield imidazole-2-chalcogenones: direct evidence for ionic liquids as proto-carbenes
resolves10.1103/PhysRevB.37.785
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
resolves10.1063/1.438980
Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, <i>Z</i>=11–18
resolves10.1063/1.438955
Self-consistent molecular orbital methods. XX. A basis set for correlated wave functions
resolves10.1063/1.444267
Self-consistent molecular orbital methods. XXIII. A polarization-type basis set for second-row elements
resolves10.1007/BF00533485
The influence of polarization functions on molecular orbital hydrogenation energies
resolves10.1080/00268979909482888
Does density functional theory contribute to the understanding of excited states of unsaturated organic compounds?
resolves10.1063/1.1501131
Failure of density-functional theory and time-dependent density-functional theory for large extended π systems
resolves10.1063/1.1590951
Long-range charge-transfer excited states in time-dependent density functional theory require non-local exchange
resolves10.1021/jp1009302
On the Molecular Structure and UV/vis Spectroscopic Properties of the Solvatochromic and Thermochromic Pyridinium-<i>N</i>-Phenolate Betaine Dye B30
resolves10.1021/jp310964k
Theoretical Study of the Preferential Solvation Effect on the Solvatochromic Shifts of <i>para</i>-Nitroaniline
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