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On Solvent Basicity: Analysis of the SB Scale

https://doi.org/10.1021/jp970239a
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inferredcites →https://doi.org/10.1002/3527601791openalex-snapshot
Solvents and Solvent Effects in Organic Chemistry
inferredcites →https://doi.org/10.1002/9780470125793.ch7openalex-snapshot
Molecular Electrostatic Potentials and Chemical Reactivity
inferredcites →https://doi.org/10.1002/jlac.199619961112openalex-snapshot
A Generalized Solvent Basicity Scale: The Solvatochromism of 5‐Nitroindoline and Its Homomorph 1‐Methyl‐5‐nitroindoline
inferredcites →https://doi.org/10.1002/poc.610020706openalex-snapshot
Hydrogen‐bonding 8. Possible equivalence of solute and solvent scales of hydrogen‐bond basicity of non‐associated compounds
inferredcites →https://doi.org/10.1007/978-1-4757-9634-6openalex-snapshot
Chemical Applications of Atomic and Molecular Electrostatic Potentials
inferredcites →https://doi.org/10.1016/b978-0-12-433841-8.x5001-9openalex-snapshot
The Chemistry of Nonaqueous Solvents
inferredcites →https://doi.org/10.1016/s0065-3276(08)60236-1openalex-snapshot
Electronic Molecular Structure, Reactivity and Intermolecular Forces: An Euristic Interpretation by Means of Electrostatic Molecular Potentials
inferredcites →https://doi.org/10.1021/ic00063a045openalex-snapshot
Addition of new donors to the E and C model
inferredcites →https://doi.org/10.1021/j100180a030openalex-snapshot
Toward a systematic molecular orbital theory for excited states
inferredcites →https://doi.org/10.1021/j100253a048openalex-snapshot
A Lewis basicity scale for nonprotogenic solvents: enthalpies of complex formation with boron trifluoride in dichloromethane
inferredcites →https://doi.org/10.1021/ja00161a003openalex-snapshot
Toward a solvent basicity scale: the calorimetry of the pyrrole probe
inferredcites →https://doi.org/10.1021/ja00236a029openalex-snapshot
Chemometrics of solvent basicity: multivariate analysis of the basicity scales relevant to nonprotogenic solvents
inferredcites →https://doi.org/10.1021/ja00418a009openalex-snapshot
The solvatochromic comparison method. I. The .beta.-scale of solvent hydrogen-bond acceptor (HBA) basicities
inferredcites →https://doi.org/10.1021/ja00463a020openalex-snapshot
An acid-base model for mixed metal dimer formation. Enthalpies of dimer cleavage and adduct formation of (.pi.-methylallyl)palladium(II) chloride dimer and a look at mixed metallomers
inferredcites →https://doi.org/10.1021/ja00508a005openalex-snapshot
Solvatochromic comparison methods. 13. Linear solvation energy relationship. 5. Correlations between infrared .DELTA..nu. values and the .beta. scale of hydrogen bond acceptor basicities
inferredcites →https://doi.org/10.1021/ja00711a029openalex-snapshot
Hydrogen-bonded complex formation. III. Thermodynamics of complexing by infrared spectroscopy and calorimetry
inferredcites →https://doi.org/10.1021/ja00819a028openalex-snapshot
Basicity. Comparison of hydrogen bonding and proton transfer to some Lewis bases
inferredcites →https://doi.org/10.1021/ja00905a001openalex-snapshot
Hard and Soft Acids and Bases
inferredcites →https://doi.org/10.1021/ja00999a006openalex-snapshot
Calorimetric studies on some hydrogen-bonded adducts
inferredcites →https://doi.org/10.1021/jo00011a060openalex-snapshot
Correlations between the solvent hydrogen bond acceptor parameter .beta. and the calculated molecular electrostatic potential
inferredcites →https://doi.org/10.1039/p29860001071openalex-snapshot
Polarity and basicity of solvents. Part 1. A thermosolvatochromic comparison method
inferredcites →https://doi.org/10.1039/p29860001081openalex-snapshot
Polarity and basicity of solvents. Part 2. Solvatochromic hydrogen-bonding shifts as basicity parameters
inferredcites →https://doi.org/10.1103/revmodphys.45.22openalex-snapshot
The Force Concept in Chemistry

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inferred← citeshttps://doi.org/10.2139/ssrn.4892996openalex-extracted
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inferred← citeshttps://doi.org/10.1002/(sici)1097-461x(1999)72:4<421::aid-qua26>3.0.co;2-3openalex-snapshot
Solvatochromism of fluorophores with an intramolecular hydrogen bond and their use as probes in biomolecular cavity sites
inferred← citeshttps://doi.org/10.1002/9780470681909.ch1openalex-snapshot
Lewis Basicity and Affinity Measurement: Definitions and Context
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0389openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.201300085openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201304069openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201504932openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cphc.200400242openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/macp.200800386openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.1281openalex-snapshot
Solution calorimetry of organic nonelectrolytes as a tool for investigation of intermolecular interactions
inferred← citeshttps://doi.org/10.1002/poc.1450openalex-snapshot
Grouping of hydrogen‐bond ability of pure solvents and their binary mixtures based on the similarity of their microscopic properties. Part 2
inferred← citeshttps://doi.org/10.1002/poc.753openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.993openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10870-020-00875-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10895-011-0948-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10953-024-01382-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11244-021-01520-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12221-019-8317-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-012513745-4/50061-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-1-895198-64-5.50016-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-1-927885-38-3.50011-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cattod.2021.10.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.10.032openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jct.2017.02.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.12.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jphotochem.2007.11.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jphotochem.2016.12.033openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2013.06.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2017.06.052openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2018.05.074openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2019.111244openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125353openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.optmat.2017.06.027openalex-snapshot
Solvatochromic benzo[h] coumarins: Synthesis, solvatochromism, NLO and DFT study
inferred← citeshttps://doi.org/10.1016/j.saa.2011.12.060openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2012.12.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0301-0104(01)00356-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0301-0104(98)00215-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1010-6030(98)00453-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.energyfuels.7b04064openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.7b12023openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00450openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr990052aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja402848copenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jp810256xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b009114fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c1jm11565kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c2nj20835kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3py01702hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c7nj00443eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0cp03816dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3qo00580aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1055/s-0043-1775398openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/00958970802087086openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/01442350500270551openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/15257770.2011.592171openalex-snapshot
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inferred← citeshttps://doi.org/10.26434/chemrxiv.14221748openalex-snapshot
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inferred← citeshttps://doi.org/10.26434/chemrxiv.14221748.v1openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/org3030023openalex-snapshot
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inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.82.336openalex-snapshot
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