Fluoride Anion Complexation by a Triptycene-Based Distiborane: Taking Advantage of a Weak but Observable C−H⋅⋅⋅F Interaction

2017 ◽  
Vol 129 (7) ◽  
pp. 1825-1830 ◽  
Author(s):  
Chang-Hong Chen ◽  
François P. Gabbaï
Keyword(s):  
Fluoride Anion ◽  
Anion Complexation

scholarly journals Unique fluoride anion complexation in basic media by 5,5-dioxophenothiazine bis(phenylurea) and bis(phenylthiourea)

Tetrahedron ◽  
2013 ◽  
Vol 69 (38) ◽  
pp. 8142-8146 ◽  
Author(s):  
Attila Kormos ◽  
Ildikó Móczár ◽  
Dávid Pál ◽  
Péter Baranyai ◽  
Tamás Holczbauer ◽  
...  
Keyword(s):  
Fluoride Anion ◽  
Anion Complexation

Fluoride anion complexation and transport using a stibonium cation stabilized by an intramolecular P=O→Sb pnictogen bond

2021 ◽  
Author(s):  
Vanessa M. Gonzalez ◽  
Gyeongjin Park ◽  
Mengxi Yang ◽  
François P. Gabbaï
Keyword(s):  
Lewis Acid ◽  
Fluoride Anion ◽  
Anion Complexation

We describe the synthesis of [o-Ph2P(=O)(C6H4)SbPh3]+ ([2]+), an intramolecularly base-stabilized stibonium Lewis acid which was obtained by reaction of [o-Ph2P(C6H4)SbPh3]+ with NOBF4. This cation reacts with fluoride anions to afford...

CHEMICAL EFFECTS IN MULTIELECTRON PROCESSES IN THE FLUORIDE ANION

1987 ◽  
Vol 48 (C9) ◽  
pp. C9-777-C9-780
Author(s):  
R. HESSABI ◽  
D. URCH
Keyword(s):  
Fluoride Anion ◽  
Chemical Effects

Synthesis of nickel selenites, their solubility and bonding in them

1982 ◽  
Vol 47 (8) ◽  
pp. 2069-2076 ◽  
Author(s):  
Miroslav Ebert ◽  
Zdeněk Mička ◽  
Ilona Peková
Keyword(s):  
Magnetic Properties ◽  
Hydrogen Bonding ◽  
Solubility Diagram ◽  
Reflectance Spectroscopy ◽  
Chloride Anion ◽  
Fluoride Anion ◽  
Infrared Absorption Spectroscopy ◽  
Magnetic Parameters ◽  
Nickel Cation ◽  
Spectrochemical Series

The solubility diagram of the NiSeO3-SeO2-H2O system at 25 °C was studied, and on its basis, Ni(HSeO3)2.2 H2O was prepared. This selenite and NiSeO3.2 H2O were investigated by infrared absorption spectroscopy and by electronic reflectance spectroscopy and their magnetic properties were determined. Based on the infrared spectra, the force constants of the selenium-oxygen bonds were determined and the hydrogen bonding was characterized. The electronic reflectance spectra and the magnetic parameters indicate an octahedral arrangement of the coordination sphere of the nickel cation and characterize the selenite anion as a ligand that in the spectrochemical series assumes a position between the fluoride anion and water and in the nephelauxetic series, between ethylenediamine and the chloride anion.

Cleavage of the Epimines of 1,6-Anhydrohexoses with Fluoride Anion

2005 ◽  
Vol 70 (12) ◽  
pp. 2075-2085 ◽  
Author(s):  
Jiří Kroutil ◽  
Klára Jeništová
Keyword(s):  
Fluoride Anion ◽  
Ring Cleavage ◽  
Protecting Group ◽  
Reaction Conditions ◽  
Aziridine Ring ◽  
Cleavage Reactions ◽  
Derivatives Of ◽  
Fluoro Derivatives

Aziridine ring cleavage reactions of five N-nosylepimines (2-6) having D-talo, D-galacto, D-manno, and D-allo configurations with potassium hydrogendifluoride under various reaction conditions have been performed. The cleavage regioselectively afforded diaxial isomers of vicinal amino-fluoro derivatives of 1,6-anhydro-β-D-gluco- and mannopyranose 7-11 in 51-94% yields. Removal of 2-nitrobenzenesulfonyl protecting group with benzenethiol has been attempted in the case of compound 10.

scholarly journals The Fluoride Anion-Catalyzed Sulfurization of Thioketones with Elemental Sulfur Leading to Sulfur-Rich Heterocycles: First Sulfurization of Thiochalcones

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 822
Author(s):  
Grzegorz Mlostoń ◽  
Jakub Wręczycki ◽  
Katarzyna Urbaniak ◽  
Dariusz M. Bieliński ◽  
Heinz Heimgartner
Keyword(s):  
Elemental Sulfur ◽  
Fluoride Anion ◽  
Ring Size ◽  
Mild Conditions ◽  
Tetrabutylammonium Fluoride ◽  
Cesium Fluoride ◽  
Secondary Reactions ◽  
Derivatives Of

Fluoride anion was demonstrated as a superior activator of elemental sulfur (S8) to perform sulfurization of thioketones leading to diverse sulfur-rich heterocycles. Due to solubility problems, reactions must be carried out either in THF using tetrabutylammonium fluoride (TBAF) or in DMF using cesium fluoride (CsF), respectively. The reactive sulfurizing reagents are in situ generated, nucleophilic fluoropolysulfide anions FS(8−x)−, which react with the C=S bond according to the carbophilic addition mode. Dithiiranes formed thereby, existing in an equilibrium with the ring-opened form (diradicals/zwitterions) are key-intermediates, which undergo either a step-wise dimerization to afford 1,2,4,5-tetrathianes or an intramolecular insertion, leading in the case of thioxo derivatives of 2,2,4,4-tetramethylcyclobutane-1,3-dione to ring enlarged products. In reactions catalyzed by TBAF, water bounded to fluoride anion via H-bridges and forming thereby its stable hydrates is involved in secondary reactions leading, e.g., in the case of 2,2,4,4-tetramethyl-3-thioxocyclobutanone to the formation of some unexpected products such as the ring enlarged dithiolactone and ring-opened dithiocarboxylate. In contrast to thioketones, the fluoride anion catalyzed sulfurization of their α,β-unsaturated analogues, i.e., thiochalcones is slow and inefficient. However, an alternative protocol with triphenylphosphine (PPh3) applied as a catalyst, offers an attractive approach to the synthesis of 3H-1,2-dithioles via 1,5-dipolar electrocyclization of the in situ-generated α,β-unsaturated thiocabonyl S-sulfides. All reactions occur under mild conditions and can be considered as attractive methods for the preparation of sulfur rich heterocycles with diverse ring-size.

Anion complexation by amido derivatives of p-tert-butyl calix[4]arene

2007 ◽  
Vol 60 (1-2) ◽  
pp. 193-196 ◽  
Author(s):  
Abdelwaheb Hamdi ◽  
Rym Abidi ◽  
Jacques Vicens
Keyword(s):  
Tert Butyl ◽  
Anion Complexation ◽  
Derivatives Of
Sign in / Sign up

Export Citation Format

Share Document