Page 147 - Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)
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I N O R G A N I C  A C I D S  A  N D  D E R I V A T I V E S         IR-8.6






                                  Replacement operation       Prefix          Infix

                                                              amid(o)        amid(o)
                                  OH ! NH 2
                                  O ! OO                      peroxy         p  eroxo
                                  O ! S                       t  hio         thio
                                  O ! Se                      seleno         seleno
                                  O ! Te                      telluro        telluro
                                  OH ! F                      fl  uoro        fluorid(o)
                                  OH ! Cl                     chloro         chlorid(o)
                                  OH ! Br                     bromo          bromid(o)
                                  OH ! I                      i  odo         iodid(o)
                                  OH ! CN                     cyano          cyanid(o)

                       Example 5  i n  S  ection IR-8.1 demonstrates the use of the infixes  f or OH ! Cl and
                       O ! S  t o  a  rrive at the name ‘arsonochloridothioic O-acid’ for the derived parent
                       HAsCl(OH)S ¼ [AsClH(OH)S], required for naming the organic derivative:

                          EtAsCl(OH)S        ethylarsonochloridothioic O-acid.

                          Functional replacement names may, of course, be used for the derived parent acids
                       themselves. However, this amounts to introducing an additional system which is not needed
                       in inorganic nomenclature. As mentioned above, additive and substitutive nomenclature can
                       always be used.


                       Example:
                           1. HAsCl(OH)S ¼ [AsClH(OH)S]
                              chloridohydridohydroxidosulfidoarsenic (additive), or
                                             5
                              chloro(hydroxy)-l -arsanethione (substitutive)

                       Nevertheless, in Table IR-8.2 several inorganic  s pecies are listed  w  hich can be regarded as
                       derived from species in Table IR-8.1 by various replacement operations, and for which the
                       common names are in fact derived by the above prefix method (e.g. ‘thiosulfuric acid’).
                          A  p roblem that would arise with the general use of the prefix variant of functional
                       replacement names is illustrated by the thio acids. The names trithiocarbonic acid,
                       tetrathiophosphoric acid, etc., would lead to anion names trithiocarbonate, t etrathiophosphate,
                       etc., which appear t o  b e a dditive names but are incorrect as such because the ligand prefix is
                       now‘sulfido’or ‘sulfanediido’ [ thusgiving t risulfidocarbonate(2 ),tetrasulfidophosphate(3 ),
                       etc.]. Section P-65.2 of Ref. 1  p  rescribes the infix-based  n  ame carbonotrithioic acid,
                       leading to the anion name carbonotrithioate, which will not be mistaken for an
                       additive  n ame.
                          A  f ew examples of other  f unctional nomenclature are also included  i n  T  able IR-8.2
                       (e.g. phosphoryl chloride, sulfuric diamide). T hese particular names are well entrenched and
                       can still be used, but t his type of nomenclature is not recommended for compounds other
                       than those  s hown. Again, additive and substitutive names may always be constructed, as
                       exemplified in the Table.


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