Page 113 - Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)
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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-6.3





                       Example:
                          24.                         ClH Si         SiH Cl
                                                         2
                                                                       2
                                                             2  H  4
                                                          HSi  Si  SiH
                                                               H
                                                        Cl Si   3    SiHCl 2
                                                         3
                                                          1          5
                                           1,1,1,5,5-pentachloro-2,4-bis(chlorosilyl)pentasilane
                                          (all other fi ve-silicon chains have fewer substituents)


           IR-6.3.2    Hydrogen substitution in boron hydrides

                       The construction of names of derivatives of boron hydrides where hydrogen atoms have
                       been replaced  b y  s ubstituent groups follows the procedures  g iven in Section IR-6.3.1. The
                       only special feature  i s t he need for specifying replacement of a  b ridging  h ydrogen atom, in
                       which case the designator ‘m-’ is used in front of the substituent group name, as in Example
                       4  b elow.


                       Examples:
                           1.                            F B
                                                          2
                                                             B   BF 2
                                                         F B
                                                          2
                                          2-(difluoroboranyl)-1,1,3,3-tetrafluorotriborane(5)

                           2.



                                                               1

                                                         5           2

                                                        4           3



                                                          =  C  H 3  =  F

                                              2-fluoro-1,3-dimethylpentaborane(9), or
                                   2-fluoro-1,3-dimethyl-2,3:2,5:3,4:4,5-tetra-mH-nido-pentaborane(9)

                           3.








                                                               =  N  H 2
                                                         diboran(6)amine


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