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and
are named "sulfoxides" and "sulfones", respectively. Specific names are formed by
placing the names of the radicals
and
(in alphabetical order) before "sulfoxide" or "sulfone". Alternatively compounds
and
may be
named from the radical R1 followed by "sulfinyl-" or "-sulfonyl-" and the name of the parent compound corresponding to
, where
is senior to
.
Note: In the latter type of nomenclature the groups
and
are named as acyl radicals substituted into a molecule
, and thus names of the type phenylsulfonyl, phenylsulfinyl, etc., are used. However, in radicofunctional nomenclature names of the type benzenesulfonyl, benzenesulfinyl,
etc., are used (see Rule C-641.7; and compare Rule C-543.3). This difference parallels that for cyclohexanecarbonyl and cyclohexylcarbonyl (see Note to Rule
C-403.2) and it applies also to derived radicals such as benzenesulfonimidoyl or phenylsulfonimidoyl, etc. (Rule C-642.4).
631.2 - The prefixes "sulfinyl-" and "sulfonyl-" are used for the bivalent groups >SO and >SO2, respectively, in conjunction with the nomenclature of assemblies of identical units (see Subsection C-0.7), when substituents are also present that have priority over these groups for citation as principal group.Examples to Rule C-631.1
631.3 - When an >SO or >SO2 group is incorporated in a ring the compound is named as an oxide.Examples to Rule C-631.2
See Recommendations'93 R-5.5.7Examples to Rule C-631.3
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