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The Journal of Organic Chemistry, ISSN 0022-3263, 02/2005, Volume 70, Issue 3, pp. 1019 - 1028
The earlier compiled self-consistent spectrophotometric basicity scale in acetonitrile (AN) was expanded to range from 3.8 to 32.0 pK a units, that is 28... 
UNCHARGED AUXILIARY BASES | PROTONATION SITES | GAS-PHASE BASICITIES | ACID-BASE EQUILIBRIA | CHEMISTRY, ORGANIC | SUBSTITUTED ANILINES | DIMETHYL-SULFOXIDE | NONPOLAR MEDIA | DISSOCIATION-CONSTANTS | PERI-NAPHTHYLENEDIAMINES | WATER
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 08/2017, Volume 2017, Issue 30, pp. 4475 - 4489
In this work we explored the relationship between the structure and solvent effects on the basicity of a large selection of conjugated N‐heterocyclic nitrogen... 
Peri effect | Nitrogen heterocycles | Hydrogen bonds | Basicity | Solvent effects | AB-INITIO | CHEMISTRY, ORGANIC | IONIZATION-CONSTANTS | PROTON SPONGES | AQUEOUS-SOLUTION | GAS-PHASE | COSMO-RS | SCALE | ACETONITRILE | TAUTOMERISM | BENZOTRIAZOLE | Quinoline | Hydrogen-ion concentration | Nitrogen | Benzene | Acetonitrile
Journal Article
Croatica Chemica Acta, ISSN 0011-1643, 12/2014, Volume 87, Issue 4, pp. 385 - 395
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2015, Volume 54, Issue 32, pp. 9262 - 9265
The potential limits of superbasicity achievable with different families of neutral bases by expanding the molecular framework are explored using DFT... 
carbenes | density functional calculations | phosphorus ylides | phosphazenes | Brønsted superbases | BASES | DESIGN | GAS-PHASE BASICITIES | BrOnsted superbases | ORGANOSUPERBASES | CHEMISTRY, MULTIDISCIPLINARY | BISPHOSPHAZENE PROTON | MOLECULES | THF | AFFINITIES | Molecular structure | Saturation | Acetonitrile | pH | Phosphorus | Joining | Mathematical models | Basicity
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2016, Volume 81, Issue 17, pp. 7349 - 7361
Experimental basicities of some of the strongest superbases ever measured (phosphonium ylides) are reported, and by employing these compounds, the experimental... 
ACID-BASE EQUILIBRIA | CHEMICAL-SHIFTS | ANIONIC-POLYMERIZATION | GAS-PHASE | CHEMISTRY, ORGANIC | NEUTRAL BRONSTED BASES | SCALE | NONPOLAR MEDIA | P4-PHOSPHAZENE BASE | C-H BONDS | BISPHOSPHAZENE PROTON | Phosphorus compounds | Chemical properties | Hydrogen-ion concentration | Analysis
Journal Article
International Journal of Mass Spectrometry, ISSN 1387-3806, 01/2019, Volume 435, pp. 61 - 68
Journal Article
ORGANIC LETTERS, ISSN 1523-7060, 11/2019, Volume 21, Issue 22, pp. 9142 - 9146
With the synthesis of N,N',N '',N'''-tetrakis(3-(dimethylamino)propyl)triaminophosphazene (TDMPP, 1), we present the first phosphazene superbase with enhanced... 
PROTON AFFINITY | DESIGN | PYRIDINE | GAS-PHASE | CHEMISTRY, ORGANIC | GUANIDINE BASES | EXTENSION | SCALE | POLYAMINOPHOSPHAZENES | PHOSPHAZENE BASES | MOLECULES
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 11/2016, Volume 22, Issue 48, pp. 17445 - 17449
The basicity scale of very weak bases has been set up in 1,2‐dichloroethane to give, for the first time, reliable quantitative insights into the basic... 
protonation | solvent effects | basicity | gas-phase reactions | phosphanes | GAS-PHASE BASICITIES | SITES | SCALE | CHEMISTRY, MULTIDISCIPLINARY | SUPERACIDS | ACIDITY | Hydrogen-ion concentration | Amides | Dichloroethane | Esters | Polarity | Basicity | Carbonyls | Solvents | Methodology | Aniline
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2012, Volume 2012, Issue 11, pp. 2167 - 2172
Phosphanes are widely used in organic chemistry. Their basicity is important in determining their behavior in solutions of different acidity. We report a study... 
Substituent effects | Phosphanes | Amines | Hydrogen bonds | Basicity | DIAMINES | COMPLEXES | CHEMISTRY, ORGANIC | PROTONATION | PHOSPHINES | GAS-PHASE | UNIFICATION | SCALE
Journal Article