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Sulfur tetrafluoride

Sulfur tetrafluoride is a chemical compound with the formula SF<sub>4</sub>. It is a colorless corrosive gas that releases dangerous hydrogen fluoride gas upon exposure to water or moisture. Sulfur tetrafluoride is a useful reagent for the preparation of organofluorine compounds, some of which are important in the pharmaceutical and specialty chemical industries.

Structure

Sulfur in SF<sub>4</sub> is in the +4 oxidation state, with one lone pair of electrons. The atoms in SF<sub>4</sub> are arranged in a see-saw shape, with the sulfur atom at the center. One of the three equatorial positions is occupied by a nonbonding lone pair of electrons. Consequently, the molecule has two distinct types of F ligands, two axial and two equatorial. The relevant bond distances are =&nbsp;164.3&nbsp;pm and =&nbsp;154.2&nbsp;pm. It is typical for the axial ligands in hypervalent molecules to be bonded less strongly.

The <sup>19</sup>F NMR spectrum of SF<sub>4</sub> reveals only one signal, which indicates that the axial and equatorial F atom positions rapidly interconvert via pseudorotation.

Synthesis and manufacture

At the laboratory scale, sulfur tetrafluoride is prepared from elemental sulfur and cobaltic fluoride

S + 4CoF<sub>3</sub> → SF<sub>4</sub> + 4CoF<sub>2</sub>

SF<sub>4</sub> is industrially produced by the reaction of SCl<sub>2</sub> and NaF with acetonitrile as a catalyst

3 SCl<sub>2</sub> + 4 NaF → SF<sub>4</sub> + S<sub>2</sub>Cl<sub>2</sub> + 4 NaCl

At higher temperatures (e.g. 225–450&nbsp;°C), the solvent is superfluous. Moreover, sulfur dichloride may be replaced by elemental sulfur (S) and chlorine (Cl<sub>2</sub>).

A low-temperature (e.g. 20–86&nbsp;°C) alternative to the chlorinative process above uses liquid bromine (Br<sub>2</sub>) as oxidant and solvent:

S(s) + 2&nbsp;Br<sub>2</sub>(l; excess) + 4KF(s) → SF<sub>4</sub>↑ + 4&nbsp;KBr(brom)

Use in synthesis of organofluorine compounds

In organic synthesis, SF<sub>4</sub> is used to convert COH and C=O groups into CF and CF<sub>2</sub> groups, respectively. The efficiency of these conversions are highly variable.

In the laboratory, the use of SF<sub>4</sub> has been superseded by the safer and more easily handled diethylaminosulfur trifluoride, (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NSF<sub>3</sub>, "DAST": This reagent is prepared from SF<sub>4</sub>:

Other reactions

Sulfur chloride pentafluoride (), a useful source of the SF<sub>5</sub> group, is prepared from SF<sub>4</sub>.

Hydrolysis of SF<sub>4</sub> gives sulfur dioxide:

SF<sub>4</sub> + 2 H<sub>2</sub>O → SO<sub>2</sub> + 4 HF

This reaction proceeds via the intermediacy of thionyl fluoride, which usually does not interfere with the use of SF<sub>4</sub> as a reagent.

When amines are treated with SF<sub>4</sub> and a base, aminosulfur difluorides result.

Toxicity

reacts inside the lungs with moisture, forming sulfur dioxide and hydrogen fluoride which forms highly toxic and corrosive hydrofluoric acid

References