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IR-7.2                                    A D D I T I V E  N O M  E N C L A T U R E





           IR-7.2      M  O N O N U C L E A R  E  N T I T I E S

                       Names of mononuclear compounds and ions, i.e. of species with a  s ingle central atom, are
                       formed by citing the appropriate prefixes for the ligands alphabetically before  t he name
                       of the central atom. Ligands occurring more than once are collected in the name  b y  m  eans
                       of multiplicative prefixes (Table IV), i.e. ‘di’, ‘tri’, ‘tetra’, etc., for simple  l igands such as
                       chlorido, benzyl, aqua, ammine and hydroxido, and ‘bis’, ‘tris’, ‘tetrakis’, etc.,  f or more
                       complex  l igands, e.g. 2,3,4,5,6-pentachlorobenzyl and triphenylphosphane. The latter
                       prefixes  a re also used to avoid any ambiguity which might attend the use of ‘di’, ‘tri’, etc.
                       Multiplicative prefixes  w  hich are not inherent parts of the ligand name do not affect
                       the alphabetical ordering.
                         Prefixes  r epresenting ligands can be separated using enclosing marks (see also Section
                       IR-9.2.2.3), and this should  b e  d one for all but the simplest ligands,  i ncluding organic
                       ligands. I n  s ome cases the use of enclosing marks is essential in order to avoid  a mbiguity,
                       as in Examples 10 and 11 below.
                         In several of the examples below, substitutive names (see Chapter  I R-6) are also
                       given. In some  c ases, however, there  i s  n o  p arent hydride available for the construction
                       of a  s ubstitutive name (see Examples  9  and 11). Note also  t hat the formulae given below
                       in square  b  rackets are coordination compound-type formulae with the central atom
                       listed first.

                       Examples:
                                                     tetrahydroxidosilicon (additive),
                           1. Si(OH) 4
                                                     or silanetetrol (substitutive)
                                                     trimethoxidoboron  o r
                           2. B(OMe) 3
                                                     tris(methanolato)boron (both  a dditive),
                                                     or trimethoxyborane (substitutive)
                           3. FClO or [ClFO]         fluoridooxidochlorine  ( additive),
                                                              3
                                                     or fluoro-l -chloranone (substitutive)
                           4. ClOCl or [OCl 2 ]      d  ichloridooxygen (additive),
                                                     or dichlorooxidane (substitutive)
                           5. [Ga{OS(O)Me} 3 ]       t  ris(methanesulfinato)gallium (additive),
                                                     or tris(methanesulfinyloxy)gallane (substitutive)
                           6. MeP(H)SiH 3 or         trihydrido(methylphosphanido)silicon (additive),
                              [SiH 3 {P(H)Me}]       or methyl(silyl)phosphane (substitutive)
                           7. NH 2 *                 hydridonitrogen(2 * )  ( additive),
                                                     or azanylidene (substitutive)
                           8. HOC(O) *               hydroxidooxidocarbon( * ) ( additive),
                                                     or hydroxyoxomethyl (substitutive)
                           9. FArH or [ArFH]         fluoridohydridoargon
                          10. [HgMePh]               m  ethyl(phenyl)mercury (additive)
                          11. [Hg(CHCl 2 )Ph]        (dichloromethyl)(phenyl)mercury




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