3.6 |
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SECTION |
3 |
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PO |
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phosphoryl |
SeO |
seleninyl |
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SO |
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sulfinyl (thionyl) |
SeO |
2 |
selenonyl |
SO |
2 |
sulfonyl (sulfuryl) |
UO |
2 |
uranyl |
S2O |
5 |
disulfuryl |
NpO |
2 |
neptunyl† |
Radicals analogous to the above containing other chalcogens in place of oxygen are named by adding the prefixes thio-, seleno-, and so on; for example, PS, thiophosphoryl; CS, thiocarbonyl.
3.1.3Cations
3.1.3.1Monatomic Cations. Monatomic cations are named as the corresponding element; for
example, Fe |
2 , iron(II) ion; Fe |
3 , iron(III) ion. |
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This principle also applies to polyatomic cations corresponding to radicals with special names |
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ending |
in |
-yl (Sec. 3.1.2.10); for example, PO |
, phosphoryl cation; NO |
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nitryl |
cation; |
2 |
cation. |
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O oxygenyl2 , |
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Use |
of the |
oxidation number and charge number extends the |
range for radicals; for example, |
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UO |
2 |
uranyl(VI) or uranyl(2 |
) cation; UO |
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, 2uranyl(V) or uranyl(1 |
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, nitrosyl cation; |
NO, |
2 |
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) cation.
3.1.3.2Polyatomic Cations. Polyatomic cations derived by addition of more protons than re-
quired to give a neutral unit |
to polyatomic anions are named by adding the ending -onium to the |
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root |
of the name of the anion |
element; for example, |
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phosphonium ion; H PH4 |
2I , iodonium ion; |
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H 3 O |
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, oxonium ion; |
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CH OH,methyl3 2 oxonium ion. |
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Exception: |
The name |
ammonium is retained |
for the |
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ammo- |
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ion; similarly forNHsubstituted4 |
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nium |
ions; for |
example, |
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ion. |
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tetrafluoroammoniumNF4 |
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Substituted ammonium ions derived from nitrogen bases with names ending in -amine receive |
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names formed by changing -amine into -ammonium. When known by a name not ending in -amine, |
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the |
cation name |
is formed by |
adding the ending -ium |
to the |
name of the base (eliding the final |
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vowel); e.g., anilinium, hydrazinium, imidazolium, acetonium, dioxanium.
Exceptions are the names uronium and thiouronium derived from urea and thiourea, respectively.
3.1.3.3 Multiple Ions from One Base. ionic charges are indicated in their names: ion.
3.1.4Anions
Where |
more than |
one ion is derived from one base, |
the |
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, hydrazinium(1NH2 |
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) ion; N H 2 |
2 |
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5 |
6, hydrazinium(2 |
See Secs. 3.1.2.2 and 3.1.2.8 for naming monatomic and certain polyatomic anions. When an organic |
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group occurs in an inorganic compound, organic nomenclature |
(q.v.) |
is followed to name the organic |
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part. |
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3.1.4.1 |
Protonated Anions. |
Ions such as |
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HSOare4recommended to be named hydrogensulfate |
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with the two words written as one following the usual practice for polyatomic anions. However, in |
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the Nomenclature of Organic |
Chemistry, |
1979 edition, hydrogen is used as a |
separate word; this |
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practice is |
followed in this Handbook. |
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† Similarly for the other actinoid elements.
INORGANIC CHEMISTRY |
3.7 |
3.1.4.2 |
Other |
Polyatomic |
Anions. |
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Names |
for other |
polyatomic anions consist of the root name |
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of the central atom with the ending -ate |
and followed by the valence of the |
central atom |
expressed |
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by its oxidation number. Atoms and groups attached to the central atom are treated as ligands in a |
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complex. |
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Examples: |
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[Sb(OH) |
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hexahydroxoantimonate(V); |
[Fe(CN |
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hexacyanoferrate(III); |
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6] |
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[Co(NO |
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hexanitritocobaltate(III); [TiO(C |
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2O |
4)2(H 2O) |
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, |
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oxobisoxalatodiaquatitanate(IV); |
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2)6] |
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[PCl6] , hexachlorophosphate(V). |
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Exceptions to the use of the root name of the central atom are antimonate, bismuthate, carbonate, |
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cobaltate, nickelate (or niccolate), nitrate, phosphate, tungstate (or wolframate), and zincate. |
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3.1.4.3 |
Anions |
of |
Oxygen. |
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Oxygen is treated in the |
same manner as other ligands with the |
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number of -oxo groups indicated by a suffix; |
for example, |
, trioxosulfate. |
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SO |
32 |
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The ending -ite, formerly used to denote a lower state of oxidation, |
may |
be retained |
in |
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names in these cases (note Sec. 3.1.5.3 also): |
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AsO |
3 |
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arsenite |
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NOO |
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peroxonitrite |
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3 |
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BrO |
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hypobromite |
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PO |
3 |
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3 phosphite* |
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ClO |
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SO 32 sulfite |
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ClO |
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chlorite |
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S2O |
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disulfite |
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IO |
hypoiodite |
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S2O |
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NO |
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nitrite |
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S2O |
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thiosulfite |
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N O2 |
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SeO |
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selenite |
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However, compounds known to be double oxides in the solid state |
are named as such; for |
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example, Cr |
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2CuO |
4 (actually |
Cr |
2O 3 · CuO) is |
chromium(III) copper(II) |
oxide |
(and |
not copper chro- |
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mite). |
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3.1.4.4 |
Isopolyanions. |
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Isopolyanions are named by indicating with numerical prefixes the num- |
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ber of atoms of the characteristic element. It is not necessary to give the number of oxygen atoms |
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when the charge of the anion or the number of cations is indicated. |
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Examples: |
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Ca |
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3 Mo |
7O 24, tricalcium 24-oxoheptamolybdate, may be shortened to tricalcium hep- |
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tamolybdate; the |
anion, |
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);S O |
2 |
2 |
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disulfate(2 |
P);O |
4 |
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,MoisO7heptamolybdate(624 |
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7 |
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2 7 |
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phate(V)(4 |
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When |
the |
characteristic |
element is |
partially or wholly present in |
a |
lower |
oxidation |
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state |
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than |
corresponds |
to |
its |
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Periodic |
Group |
number, |
oxidation |
numbers |
are |
used; |
for |
example, |
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[O2HP9O |
9PO 3 H]2 , dihydrogendiphosphate(III,V)(2 |
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A bridging group should be indicated by adding the Greek letter |
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immediately before its names |
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and separating this from the rest of the complex by a hyphen. The atom or atoms of the characteristic |
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element to which the bridging atom is bonded, is indicated by numbers. |
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Examples: |
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[O3 P9S 9PO2 9O |
9PO 3]5 , 1,2- -thiotriphosphate(5 |
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[S3 P9O |
9PS2 9O |
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5 |
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) |
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9PS3 ] , di- -oxo-octathiotriphosphate(5 |
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* Named for esters formed from the hypothetical acid P(OH) |
3 . |