- In
organic chemistry, a
sulfide (British
English sulphide) or
thioether is an
organosulfur functional group with the
connectivity R−S−R' as
shown on right...
-
refers to the
linkage C–S–C,
although the term
thioether is less ambiguous. For example, the
thioether dimethyl sulfide is CH3–S–CH3.
Polyphenylene sulfide...
-
methylthiomethane is an
organosulfur compound with the
formula (CH3)2S. The
simplest thioether, it is a
flammable liquid that
boils at 37 °C (99 °F) and has a characteristic...
-
formula (CH3CH2)2S. It is a colorless,
malodorous liquid.
Although a
common thioether, it has few applications.
Diethyl sulfide is a by-product of the commercial...
-
Transition metal thioether complexes comprise coordination complexes of
thioether (R2S) ligands. The
inventory is extensive. As the
simplest thioether, dimethyl...
-
organic reaction whereby an
alkyl sulfoxide rearranges to an α-acyloxy–
thioether (monothioacetal-ester) in the
presence of
acetic anhydride. The stoichiometry...
-
organic reaction between a
thiol (R−SH) and an
alkene (R2C=CR2) to form a
thioether (R−S−R'). This
reaction was
first reported in 1905, but it
gained prominence...
- In enzymology, a
thioether S-methyltransferase (EC 2.1.1.96) is an
enzyme that
catalyzes the
chemical reaction. S-adenosyl-L-methionine +
dimethyl sulfide...
-
aurous ion, is the most
common oxidation state with soft
ligands such as
thioethers, thiolates, and organophosphines. Au(I)
compounds are
typically linear...
-
residue + 5
Exocyclic double bond + 5
acetate group + 0
Ether group + 6
Thioether group + 30 bromine,
chlorine + 5
secondary amine group + 60
Table 1. Rules...
