Page 78 - Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)

T A B L E I I I T A B L E S

Table III Continued

ocine Ending of parent names of eight-membered heteromonocycles with the maximum number
of non-cumulative double bonds in Hantzsch–Widman nomenclature, cf. Section IR-
6.2.4.3.
ol Suffix specifying substitution af a h ydrogen atom in a p arent hydride for the group OH,
accompanied by locants and multiplicative prefixes if appropriate, e.g. silanol, SiH 3 OH;
trisilane-1,3-diol, SiH 2 (OH)SiH 2 SiH 2 OH.
Ending of corresponding suffixes ‘thiol’, ‘selenol’, ‘tellurol’ for SH, SeH and TeH,
respectively.
olane General ending of parent names of five-membered saturated heteromonocycles in
Hantzsch–Widman nomenclature, cf. I R-6.2.4.3. See also ‘olidine’.
olate Suffix specifying substitution of a h ydrogen atom in a p arent hydride for the substituent

O , a ccompanied by locants and multiplicative prefixes if appropriate, e.g. silanolate,

SiH 3 O ; t risilane-1,3-diolate, SiH 2 (O )SiH 2 SiH 2 O .

Ending of corresponding suffixes ‘thiolate’, ‘selenolate’, ‘tellurolate’ for S , Se and

Te , r espectively.
olato Modification of the suffix ‘olate’ used when the anion in question acts as a l igand.
ole Ending of parent names of five-membered heteromonocycles with the maximum
number of non-cumulative double bonds in Hantzsch–Widman nomenclature, cf. S ection
IR-6.2.4.3.
olidine Ending of parent names of five-membered nitrogen-containing saturated heteromonocycles
in Hantzsch–Widman nomenclature, cf. S ection IR-6.2.4.3.
onane Ending of parent names of nine-membered saturated heteromonocycles in Hantzsch–
Widman nomenclature, cf. S ection IR-6.2.4.3.

onate Ending of names of anions and esters of ‘onic’ oxoacids, e.g. boronate, phosphonate,
tetrathionate.
onato Modification of the ‘onate’ ending of an anion used when the anion acts as a l igand.
Ending of prefixes of certain anionic substituent groups, e.g. phosphonato, P(¼O)(O ) 2 ;

sulfonato, S(¼O) 2 (O ).

one Suffix specifying the substitution of two hydrogen atoms on the same skeletal atom in
a p arent hydride for the substituent ¼O, accompanied by locants and multiplicative
prefixes as appropriate, e.g. phosphanone, HP¼O; pentane-2,4-dione,
CH 3 C(¼O)CH 2 C(¼O)CH 3 .
Ending of corresponding suffixes ‘thione’, ‘selenone’, ‘tellurone’ for ¼S, ¼Se and ¼Te,
respectively.

onic Ending of the parent names of acids of the types HXO(OH) 2 (X¼N, P, As, Sb), e.g.
stibonic acid; HXO 2 (OH) (X ¼ S, Se, Te), e.g. sulfonic acid; and of boronic acid,
HB(OH) 2 . S ee Table IR-8.1.
Ending of the parent names dithionic, trithionic, etc., a cids (see Table IR-8.1).
onine Ending of parent names of nine-membered heteromonocycles with the maximum
number of non-cumulative double bonds in Hantzsch–Widman nomenclature, cf. S ection
IR-6.2.4.3.
onite Ending of names of anions and esters of ‘onous’ oxoacids, e.g. phosphonite, tetrathionite.
onito Modification of the ‘onite’ ending of an anion name used when the anion acts as a l igand.

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