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IR-9.2                                  C O O R D I N A T I O N  C O M  P O U N D S





                         For example, one would use diammine  f or (NH 3 ) 2 , b ut bis(methylamine) for (NH 2 Me) 2 ,
                       to make a distinction from dimethylamine. There is no elision of vowels or use of a h yphen,
                       e.g. in tetraammine  a nd similar names.

           IR-9.2.2.3  Representing ligands in names

                       Systematic and alternative names for some common ligands are given  i n  T ables V II and IX.
                       Table VII c ontains the names of common organic ligands whereas Table IX contains t he names
                       of other simple m olecules and ions that may act as ligands. The general features are as follows:

                       (i)  Names of anionic ligands,  w  hether  i norganic or organic, are modified to end in ‘o’.
                           In general, i f t he anion name ends in ‘ide’, ‘ite’ or ‘ate’, the final ‘e’ is replaced  b y  ‘ o’,
                           giving ‘ido’, ‘ito’ and ‘ato’, respectively. In particular, alcoholates, thiolates,
                           phenolates, carboxylates, partially dehydronated amines, phosphanes, etc.  a re in this
                           category. Also, it follows that halide ligands are named fluorido, chlorido, bromido and
                           iodido, and coordinated cyanide is named cyanido.
                              Initscomplexes,exceptforthoseof molecular hydrogen,hydrogen i s a lwaystreated a s
                           anionic. ‘Hydrido’ i s u sed  f or hydrogen c oordinating to all elements including b oron. 3
                                                                                 4
                       (ii) Names of neutral and cationic ligands,  i ncluding organic ligands, are used without
                           modification (even if they carry the endings ‘ ide’, ‘ite’ or ‘ate’; see Examples 8  a nd 14
                           below).
                       (iii) Enclosing  m  arks are required for neutral and cationic ligand names, for names of
                           inorganic anionic ligands containing multiplicative prefixes (such  a s t riphosphato), for
                           compositional names (such a s c arbon disulfide), for names of substituted organic ligands
                           (even if there is no ambiguity in their use), and wherever necessary t o  a void ambiguity.
                           However, common ligand names such as aqua, ammine, carbonyl, n itrosyl, methyl, e thyl,
                           etc., do not require enclosing marks, unless there is ambiguity when they are absent.
                       (iv) Ligands binding to metals through carbon atoms are treated in Chapter  I R-10 on
                           organometallic compounds.

                       Examples:

                              Formula            Ligand name
                           1. Cl                 chlorido

                           2. CN                 cyanido
                           3. H                  hydrido 3
                                                         3
                                  2
                                                              2

                           4. D or H              deuterido or [ H]hydrido 3
                           5. PhCH 2 CH 2 Se     2-phenylethane-1-selenolato
                           6. MeCOO              acetato or ethanoato
                           7. Me 2 As            dimethylarsanido
                                                 acetamide (not acetamido)
                           8. MeCONH 2
                           9. MeCONH              acetylazanido or acetylamido (not acetamido)
                                                 methanamine
                          10. MeNH 2

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