Page 186 - Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)

Subject Index

Pearson notation, 57, 241–242 Stiboric acid, 129
phase composition, 237–238 Stiborous acid, 129
variation, 3 5, 238 Stock number (see oxidation number)
phase nomenclature, 241–242 Stoichiometric descriptors, for addition
point defect notation (see Kro ¨ger–Vink compounds, 33, 80–81
notation), 238–241 Stoichiometric names (see also generalized
polymorphism, 245–246 stoichiometric names), 6, 69–75
polytypes, 246 binary compounds, 69–70
use of crystal systems, 246 boron hydrides, 8 9–90
site type, 1 9, 21, 29 ions, 7 0–75
solutions, 236 anions, 72–75
structural t ype, 34 cations, 7 0–72
unit cell t winning, 244–245 order of components, 6, 75–76
Vernier structures, 242–243 order of elements, 69
Solidus, in names of addition compounds, table, 280–336
27 Stoichiometric phases, 236
Spaces in names, 30 Strike-through parentheses, in formulae of
Specific i sotopic l abelling, 64–65 polymers, 22, 56, 61
Square brackets Structural affixes, 259
in formulae, 17–19 Structural descriptors, 166, 168
to enclose coordination entity, in boron hydride nomenclature, 90–92
17–19, 59, 113–117 in formulae, 67
to enclose structural f ormulae, 19 for polynuclear clusters, 170, 172–174
isotopically labelled compounds, 6 4–65 Structural formulae
in names, 17, 19–20 enclosing marks, 55–56
Square planar complexes, configuration of ligands, 261–268
index, 180–181 Subscripts
Square pyramidal complexes, specifying to indicate a tomic n umber, 32, 47–48
configuration, 183–184 Substituent groups
Standard bonding numbers, 84 in boron hydrides, 1 04–105
and mononuclear acyclic parent derived from metallocenes, 225–226
hydrides, 8 6 derived from parent hydrides, 101–104,
Stereochemical p riorities, CIP rules, 44 108–110
Stereochemistry, atom numbering, 40 and enclosing marks, 22–23
Stereochemical d escriptors (or ligands forming multiple m etal–carbon
stereodescriptors), 144 bonds, 213–215
and enclosing marks, 22–24 in organometallics, 203
polyhedral s ymbols, 175–179 named from parent hydrides, 2 04, 2 07
Stereoisomers of coordination compounds, table of names, 280–336
175 Substitutive nomenclature, 6–7, 83–110
Stibine, o bsolete n ame for stibane, 8 5 ( see vs. a dditive nomenclature, 83–84,
footnote e ) 113–118
Stibinic acid, 129 for parent hydrides, 1 02–103
Stibinous acid, 129 boron hydrides
Stibonic a cid, 129 hydrogen atom distribution,
Stibonous acid, 129 93–94

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