The urea-based receptor 1 (1-(7-nitrobenzo[1,2,5]oxadiazol-4-yl)- 3-(4-nitrophenyl)urea, LH), interacts with X- ions in MeCN, according to two consecutive steps: 1) formation of a hydrogen-bond complex [L-H···X]-; 2) deprotonation of LH to give L- and [HX2]-, as shown by spectrophotometric and 1H NMR titration experiments. Step 2) takes place with more basic anions (fluoride, carboxylates, dihydrogenphosphate), while less basic anions (Cl-, NO2-, NO3-) do not induce proton transfer. On crystallisation from a solution containing LH and excess Bu4NF, the tetrabutylammonium salt of the deprotonated urea derivative (Bu4N[L]) was isolated and its crystal and molecular structure determined.

Anion-Induced Urea Deprotonation

BOIOCCHI, MASSIMO;FABBRIZZI, LUIGI;LICCHELLI, MAURIZIO;MONZANI, ENRICO
2005-01-01

Abstract

The urea-based receptor 1 (1-(7-nitrobenzo[1,2,5]oxadiazol-4-yl)- 3-(4-nitrophenyl)urea, LH), interacts with X- ions in MeCN, according to two consecutive steps: 1) formation of a hydrogen-bond complex [L-H···X]-; 2) deprotonation of LH to give L- and [HX2]-, as shown by spectrophotometric and 1H NMR titration experiments. Step 2) takes place with more basic anions (fluoride, carboxylates, dihydrogenphosphate), while less basic anions (Cl-, NO2-, NO3-) do not induce proton transfer. On crystallisation from a solution containing LH and excess Bu4NF, the tetrabutylammonium salt of the deprotonated urea derivative (Bu4N[L]) was isolated and its crystal and molecular structure determined.
2005
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Esperti anonimi
Inglese
Internazionale
STAMPA
11
10
3097
3104
8
acid–base reactions; anions; hydrogen bonds; supramolecular chemistry; urea
http://www.chemeurj.org
6
info:eu-repo/semantics/article
262
Boiocchi, Massimo; DEL BOCA, L.; ESTEBAN GOMEZ, D.; Fabbrizzi, Luigi; Licchelli, Maurizio; Monzani, Enrico
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/134429
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