“…Binding of H2PO4 -in the stoichiometry 1:2 has already been reported for bisurea derivatives. 29,35 Later, it was shown that stoichiometry 1:2 can be due to the formation of two 36 or 3 intermolecular H-bonds between two H2PO4 -anions. 37 This cooperative effect additionally stabilizes 1:2 stoichiometries rendering them more stable than the …”
Blažek, V.; Molčanov, K.; Mlinarić-Majerski, K.; Kojić-Prodić, B.; Basarić, N. Adamantane bisurea derivatives: anion binding in the solution and in the solid state. Tetrahedron. 2013, 69, 517-526. DOI: 10.1016/j.tet.2012
“…Binding of H2PO4 -in the stoichiometry 1:2 has already been reported for bisurea derivatives. 29,35 Later, it was shown that stoichiometry 1:2 can be due to the formation of two 36 or 3 intermolecular H-bonds between two H2PO4 -anions. 37 This cooperative effect additionally stabilizes 1:2 stoichiometries rendering them more stable than the …”
Blažek, V.; Molčanov, K.; Mlinarić-Majerski, K.; Kojić-Prodić, B.; Basarić, N. Adamantane bisurea derivatives: anion binding in the solution and in the solid state. Tetrahedron. 2013, 69, 517-526. DOI: 10.1016/j.tet.2012
“…This was initially surprising, because thioureas are known to be excellent hydrogen bond donors-better than ureas. 26 However, in this case, the hydrogen bond acceptor would have to be, predominantly, C<img border="0" alt="double bond; length as m-dash" src="http://cdn.els-cdn.com/sd/entities/dbnd" class="glyphImg">S. Sulfur is a poor hydrogen bond acceptor, and we therefore propose that compound 1-thiourea is unable to establish an effective sample-spanning hydrogen-bonded network due to these ineffective hydrogen-bond acceptor groups.…”
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AbstractWe report the synthesis of a family of gelators in which alkyl chains are connected to the amino groups of L-lysine methyl ester using a range of different hydrogen bonding linking groups (carbamate, amide, urea, thiourea and diacylhydrazine) using simple synthetic methodology based on isocyanate or acid chloride chemistry. The ability of these compounds to gelate organic solvents such as toluene or cyclohexane can be directly related to the ability of the linking group to form intermolecular hydrogen bonds. In general terms, the ability to structure solvents can be considered as:thiourea
“…Accordingly, a variety of sensing systems, involving amide, urea (thiourea), hydrazine, calix[n]arenes, hydroxyl derivatives have been employed for the selective detection of H 2 PO 4 - [12][13][14][15] . While phenol commonly plays an important role in the anion binding site of biological system, very little investigation has been carried out to develop H 2 PO 4 − sensors bearing phenol and carbazole groups.…”
Two fluorescent anion sensors bearing phenol, carbazole-NH and -NO 2 group were designed and synthesized. They both exhibited highly binding ability for , respectively. Theoretical investigation indicated it was the highest HOMO to induce the red-shift phenomena of two sensors.
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