Insight into the deprotonation at the half-equivalence point of (thio)amido-benzimidazoles in the presence of anions-Reference-Cited by-同舟云学术

Insight into the deprotonation at the half-equivalence point of (thio)amido-benzimidazoles in the presence of anions

Published:2017 Issue:35 Volume:15 Page:7263-7266
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Koeller S.¹²³⁴,Lescure M.-H.¹²³⁴,Davies C.¹²³⁴,Desvergne J.-P.¹²³⁴,Massip S.¹⁵⁶⁷⁴,Bibal B.¹²³⁴^ORCID

Affiliation:

1. Université de Bordeaux

2. Institut des Sciences Moléculaires UMR 5255

3. 33405 Talence

4. France

5. IECB

6. CNRS UMS 3033/INSERM US001

7. 33607 Pessac

Abstract

Three crystallographic structures highlight the acid–base half-equivalence point of hydrogen-bond donor (thio)amido-benzimidazoles induced by fluoride or benzoate salts with concomitant hydrogen-bonding and deprotonation as a merged synergic process.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01704A

Reference42 articles.

1. What Anions Do to N−H-Containing Receptors

2. Recognition and sensing of fluoride anion

3. Advances in Anion Supramolecular Chemistry: From Recognition to Chemical Applications

4. Anion Recognition in Water: Recent Advances from a Supramolecular and Macromolecular Perspective

5. Anion Recognition and Sensing: The State of the Art and Future Perspectives

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