A very short-strong hydrogen bond (<2 Å, >20kcal/mol) is found in the monoanion of certain dicarboxylic acids derived from maleic and dialkylmalonic acids. Certain aromatic diamines that are known as proton sponge have exceptionally high basicity (pKa) and are only monoprotonated with strong acids like percloric acid. The closed proximity between the two basic centers provokes a strong steric interaction that is relieved upon protonation. Similar effects are found in dicarboxylic acids (hydrogen maleate and hydrogen dialkylmalonates) that present a very short distance between the two oxygens and a short-strong hydrogen bond
A series of seven 2:1 molecular complexes of urea (U) and methyl ureas with di-carboxylic acids (A) ...
The synthesis and X-ray structural investigations of sterically hindered aromatic tethered carboxyli...
New superbases, those organic compounds whose basicities are greater than that of proton sponge, are...
A very short-strong hydrogen bond (, >20kcal/mol) is found in the monoanion of certain dicarboxylic ...
Certain aromatic diamines (the “proton sponges”) are found to have exceptionally high basicity const...
A very short-strong hydrogen bond (<2 Å, >20kcal/mol) is found in the monoanion of certain dic...
In a study of 101 crystal structures of carboxylic acids we have observed a clear trend in the diffe...
.ABSTRACT OF THE DISSERTATIONIn Search of a Low Barrier Hydrogen Bond in Proton Bridged DiaminesbySe...
Medium and strong hydrogen bonds give rise to broad vibrational features frequently spanning several...
Hydrogen bonds play a crucial role in chemistry and biology. Numerous experimental and theoretical s...
The main focus of this research was to examine the molecular complexes formed by the proton sponge m...
Short hydrogen bonds (H-bonds) have been proposed to play key functional roles in several proteins. ...
The catemer is an infinite one-dimensional pattern formed by the carboxylic acid group in crystals, ...
Ab initio calculations are used to compare the abilities of the aromatic groups of the Phe, Tyr, Trp...
Witt M, Grützmacher H-F. Effects of internal hydrogen bonds between amide groups: Gas-phase basicity...
A series of seven 2:1 molecular complexes of urea (U) and methyl ureas with di-carboxylic acids (A) ...
The synthesis and X-ray structural investigations of sterically hindered aromatic tethered carboxyli...
New superbases, those organic compounds whose basicities are greater than that of proton sponge, are...
A very short-strong hydrogen bond (, >20kcal/mol) is found in the monoanion of certain dicarboxylic ...
Certain aromatic diamines (the “proton sponges”) are found to have exceptionally high basicity const...
A very short-strong hydrogen bond (<2 Å, >20kcal/mol) is found in the monoanion of certain dic...
In a study of 101 crystal structures of carboxylic acids we have observed a clear trend in the diffe...
.ABSTRACT OF THE DISSERTATIONIn Search of a Low Barrier Hydrogen Bond in Proton Bridged DiaminesbySe...
Medium and strong hydrogen bonds give rise to broad vibrational features frequently spanning several...
Hydrogen bonds play a crucial role in chemistry and biology. Numerous experimental and theoretical s...
The main focus of this research was to examine the molecular complexes formed by the proton sponge m...
Short hydrogen bonds (H-bonds) have been proposed to play key functional roles in several proteins. ...
The catemer is an infinite one-dimensional pattern formed by the carboxylic acid group in crystals, ...
Ab initio calculations are used to compare the abilities of the aromatic groups of the Phe, Tyr, Trp...
Witt M, Grützmacher H-F. Effects of internal hydrogen bonds between amide groups: Gas-phase basicity...
A series of seven 2:1 molecular complexes of urea (U) and methyl ureas with di-carboxylic acids (A) ...
The synthesis and X-ray structural investigations of sterically hindered aromatic tethered carboxyli...
New superbases, those organic compounds whose basicities are greater than that of proton sponge, are...