Literature DB >> 15827647

Urea vs. thiourea in anion recognition.

David Esteban Gómez1, Luigi Fabbrizzi, Maurizio Licchelli, Enrico 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]-.

Entities:  

Year:  2005        PMID: 15827647     DOI: 10.1039/b500123d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  26 in total

1.  Pyrrole based Schiff bases as colorimetric and fluorescent chemosensors for fluoride and hydroxide anions.

Authors:  Sivan Velmathi; Vijayaraghavan Reena; Sivalingam Suganya; Sambandam Anandan
Journal:  J Fluoresc       Date:  2011-08-13       Impact factor: 2.217

2.  A colorimetric and ratiometric fluorescent chemosensor for fluoride based on proton transfer.

Authors:  Chuandong Jia; Biao Wu; Jianjun Liang; Xiaojuan Huang; Xiao-Juan Yang
Journal:  J Fluoresc       Date:  2009-10-17       Impact factor: 2.217

Review 3.  Artificial receptors for the recognition of phosphorylated molecules.

Authors:  Amanda E Hargrove; Sonia Nieto; Tianzhi Zhang; Jonathan L Sessler; Eric V Anslyn
Journal:  Chem Rev       Date:  2011-09-12       Impact factor: 60.622

4.  Tuning Photophysical and Electrochemical Properties of Phosphorescent Heteroleptic Iridium Complex Salts-as Chemosensors.

Authors:  J Jayabharathi; R Sathishkumar; V Thanikachalam; K Jayamoorthy
Journal:  J Fluoresc       Date:  2013-10-11       Impact factor: 2.217

5.  An exclusive fluoride receptor: Fluoride-induced proton transfer to a quinoline-based thiourea.

Authors:  Ismet Basaran; Maryam Emami Khansari; Avijit Pramanik; Bryan M Wong; Alamgir Hossain
Journal:  Tetrahedron Lett       Date:  2014-02-19       Impact factor: 2.415

6.  Chiral Thioureas Promote Enantioselective Pictet-Spengler Cyclization by Stabilizing Every Intermediate and Transition State in the Carboxylic Acid-Catalyzed Reaction.

Authors:  Rebekka S Klausen; C Rose Kennedy; Alan M Hyde; Eric N Jacobsen
Journal:  J Am Chem Soc       Date:  2017-08-22       Impact factor: 15.419

7.  Solution and solid-phase halogen and C-H hydrogen bonding to perrhenate.

Authors:  Casey J Massena; Asia Marie S Riel; George F Neuhaus; Daniel A Decato; Orion B Berryman
Journal:  Chem Commun (Camb)       Date:  2015-01-28       Impact factor: 6.222

8.  A density functional study towards substituent effects on anion sensing with urea receptors.

Authors:  Amrita Ghosh; D Amilan Jose; Amitava Das; Bishwajit Ganguly
Journal:  J Mol Model       Date:  2010-02-17       Impact factor: 1.810

9.  Indole-3-thio-uronium nitrate.

Authors:  Martin Lutz; Anthony L Spek; Erwin P L van der Geer; Gerard van Koten; Robertus J M Klein Gebbink
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2007-12-06

10.  Fluoride-triggered ESPT in the binding with sal(oph)en.

Authors:  Kai Liu; Jianzhong Huo; Bolin Zhu; Ran Huo
Journal:  J Fluoresc       Date:  2012-05-16       Impact factor: 2.217

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