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S U B S T I T U T I V E  N O M  E N C L A T U R E                   IR-6.4





                           3. MeNH                         methylazanide,  or   methylamide,   or
                                                           methanaminide (all substitutive, see Section
                                                           P-72.2 of Ref. 1)
                           4.
                                1   2  3  4  5   6  7  8  9

                               SnH 2 O Sn H 2 O Sn H 2 O Sn H 2 O Sn Cl 3
                                                           9,9,9-trichloropentastannoxan-1-ide
                           5. [BH 3 CN]                    cyanoboranuide (from borane),
                                                           or cyanidotrihydridoborate(1 )  ( additive)
                                                                     5
                           6. [PF 6 ]                      hexafluoro-l -phosphanuide (from phosphane),
                                                           or hexafluoridophosphate(1 )  ( additive)

           IR-6.4.7    Radicals  a nd substituent groups

                       Radicals and substituent groups derived from parent hydrides by removal of one or more
                       hydrogen atoms are named by modifying the parent hydride name as follows:

                       (i)  removal of one hydrogen atom: add suffix ‘yl’ (eliding final ‘e’ of parent hydride
                            name);
                       (ii)  removal of two or more hydrogen atoms: add suffix ‘yl’ with appropriate
                            multiplicative prefix (no vowel elision).
                          The suffix ‘ylidene’ is used on a  s ubstituent group if a  d ouble bond is implied when a
                       skeletal atom has formally  l ost two hydrogen atoms. If a  t riple bond is implied, the ending
                       ‘ylidyne’ is used. With these endings, the ending ‘e’ of the parent hydride name is again elided.
                          For radicals, if two hydrogens are removed from the same atom the suffix ‘ylidene’ is used.
                          Locants m  ay be needed  t o  i ndicate the skeletal atoms from which hydrogen atoms have
                       been removed. Such locants are placed immediately before the suffix. When numbering the
                       structure,  t he positions where hydrogen atoms were removed take precedence  o  ver
                       unsaturation, as in Example 9  b elow.
                          Radicals may also be named using additive nomenclature, see Section IR-7.1.4 and
                       examples in subsequent sections of Chapter IR-7.


                       Examples:

                           1. NH 2 *                                    azanylidene
                                 *
                           2. PH 2 and H 2 P                            phosphanyl
                           3. PH 2 *  and HP¼                           phosphanylidene
                           4. HP5                                       phosphanediyl
                           5. P                                         phosphanylidyne
                                  *                                      3
                           6. H 2 Br and H 2 Br                         l -bromanyl
                                     *
                           7. H 2 NNH and H 2 NNH                       diazanyl or hydrazinyl
                                     *
                           8.  * HNNH and  HNNH                         diazane-1,2-diyl or
                                                                        hydrazine-1,2-diyl
                                                      |
                                     *     *
                           9. HP¼NP NHPH and HP¼NPNHPH                  triphosphaz-4-ene-1,3-diyl

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