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Urea vs. thiourea in anion recognition

Organic & Biomolecular Chemistry · 2005 · Vol. 3(8) · pp. 1495–1500
David Esteban‐GómezLuigi FabbrizziMaurizio LicchelliEnrico Monzani

Abstract

Neutral anion receptors (LH) form stable 1 : 1 H-bond [LH...X]- complexes with carboxylates, halides and phosphate (X-). Some of the [LH...X]- complexes, in presence of an excess of X-, release an HX fragment, with formation of [HX2]- and the deprotonated receptor L-. The tendency towards deprotonation increases with the acidity of the receptor and with the stability of the [HX2]- self-complex. Thus, the more acidic thiourea containing receptor deprotonates in the presence all the investigated anions except chloride, whereas the less acidic urea containing receptor undergoes deprotonation only in the presence of fluoride, due to the high stability of [HF2]-.

Molecular Sensors and Ion DetectionNeuroscience and Neuropharmacology ResearchLuminescence and Fluorescent MaterialsChemistryDeprotonationThioureaUreaHalideMedicinal chemistryChlorideInorganic chemistryFluorideReceptor

Funding

  • European Commission
  • Ministero dell'Università e della Ricerca
Citations
349
FWCI
12.33
field-weighted impact
References
17
Percentile
99%
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Citations per year
Cited by
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References
Anion Recognition and Sensing: The State of the Art and Future Perspectives
Angewandte Chemie International Edition · 2001 · 3,559 citations
The Hydrogen Bond in the Solid State
Angewandte Chemie International Edition · 2002 · 6,098 citations
Equilibrium acidities in dimethyl sulfoxide solution
Accounts of Chemical Research · 1988 · 2,811 citations
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