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IR-6.2                               S U B S T I T U T I V E  N O M  E N C L A T U R E





                       Examples:
                           1.
                                1  2  3  4
                              H 5 SSSH 4 SH
                                   6
                                6
                                                        6
                                                     6
                              1l ,3l -tetrasulfane (not 2l ,4l )
                           2.
                                1  2  3  4  5
                              HSSH 4 SH 4 SH 2 SH
                                                         4
                                6
                                                            6
                                                               6
                                   6
                                      4
                              2l ,3l ,4l -pentasulfane (not 2l ,3l ,4l )
                           3.
                              H 4 PPH 3 PH 3 PH 4
                                5  5  5   5
                              ll ,2l ,3l ,4l -tetraphosphane
                           4.
                              HPbPbPbH
                                2
                                       2
                                   2
                              1l ,2l ,3l -triplumbane
           IR-6.2.2.3  Unsaturated homonuclear acyclic  h ydrides
                       Chains containing unsaturation are accommodated in substitutive nomenclature by the
                       methods used with alkenes and alkynes (see Section P-31.1 of Ref. 1), i.e. the name of the
                       corresponding saturated chain hydride is modified by replacing the ‘ane’ ending with ‘ene’ in
                       the case of a d ouble b ond and ‘yne’ in the case of a t riple bond. If there is one of each, the ending
                       becomes ‘en’ . . .‘yne’ with appropriate locants; ‘diene’ is used when there are two double
                       bonds, and so on. In each case the position(s) o f u nsaturation is (are) indicated by (a) numerical
                       locant(s) immediately preceding the suffix(es). Locants are chosen  t o  b e a s l ow as possible.
                       Examples:
                           1.
                              HN¼NH                   diazene
                           2.
                              HSb¼SbH                 distibene
                           3.
                                1  2  3 4  5
                                                      pentaaz-2-ene (not pentaaz-3-ene)
                              H 2 NN¼NNHNH 2
                       Unsaturated acyclic hydrides are not classified as parent hydrides.  B  ecause of the
                       hierarchical rules of substitutive nomenclature, the numbering of the double and triple bonds
                       may not be fixed until various g roups and modifications have been numbered. (See Section
                       IR-6.4.9 for an example.)

           IR-6.2.2.4  Homonuclear monocyclic parent hydrides

                       There are three main ways  o f  g iving  p arent names to homonuclear monocyclic hydrides:

                       (i)  by using  t he Hantzsch–Widman (H–W) name (see Section IR-6.2.4.3  a nd Section
                           P-22.2 of Ref. 1);
                       (ii)  by using the relevant  r eplacement prefix (‘a’ term) from Table X  t ogether  w  ith the
                           appropriate multiplicative  p  refix to indicate replacement of carbon atoms in the
                           corresponding carbocyclic compound name (see Section P-22.2 of Ref. 1);
                       (iii) by adding the prefix ‘cyclo’ to the name o f t he corresponding unbranched, unsubstituted
                           chain (see Sections IR-6.2.2.1 to IR-6.2.2.3 and Section P-22.2 of Ref. 1).


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