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O R G A N O M  E T A L L I C  C  O M  P O U N D S                  IR-10.3





                           9. MgIMe
                              magnesium iodide methanide (compositional name)
                              [MgI(Me)]
                              iodido(methanido)magnesium (additive name of coordination type)
                              [MgMe]I
                              methylmagnesium iodide (compositional n ame with formally  e lectropositive
                              component named using additive nomenclature)
                              [MgI(Me)] n
                              poly[iodido(methanido)magnesium], or poly[iodido(methyl)magnesium]

           IR-10.3.3   Organometallic compounds of groups  1 3–16

                       Organometallic compounds of the elements of groups 13–16  a re named according to the
                       substitutive system of nomenclature, dealt with in Chapter  I R-6. Thus, the name of the
                       parent hydride (formed in accordance with the rules of Section IR-6.2)  i s  m  odified by a
                       prefix for each substituent  r eplacing a  h ydrogen atom of the parent hydride. The prefix
                       should be in appropriate substituent  f orm (chloro,  m  ethyl, sulfanylidene, etc.)  a nd not in
                       ligand form (chlorido, m  ethanido, sulfido, etc.).
                          Where there is more than one kind of substituent, the prefixes  a re cited in alphabetical
                       order before the name o f t he parent hydride, parentheses being used to avoid  a mbiguity, and
                       multiplicative prefixes being used as necessary. Non-standard bonding numbers are
                       indicated using the l-convention (see Section IR-6.2.2.2). An overview of the rules for
                       naming substituted derivatives of parent hydrides is given i n S ection IR-6.3, w hile a d etailed
                       exposition may be found in Ref. 3.


                       Examples:
                           1. AlH 2 Me           methylalumane
                                                 triethylalumane
                           2. AlEt 3
                           3. Me 2 CHCH 2 CH 2 In(H)CH 2 CH 2 CHMe 2
                              bis(3-methylbutyl)indigane
                                                 triethenylstibane, or trivinylstibane
                           4. Sb(CH¼CH 2 ) 3
                                                             5
                                                 pentamethyl-l -stibane
                           5. SbMe 5
                           6. PhSb¼SbPh          d  iphenyldistibene
                                                 dichlorodimethylgermane
                           7. GeCl 2 Me 2
                                                 methyltris(methylsulfanyl)germane
                           8. GeMe(SMe) 3
                           9. BiI 2 Ph           diiodo(phenyl)bismuthane

                                                 hexaethyldiplumbane
                          10. Et 3 PbPbEt 3
                                                          2
                                                 dimethyl-l -stannane
                          11. SnMe 2
                          12. BrSnH 2 SnCl 2 SnH 2 (CH 2 CH 2 CH 3 )
                              1-bromo-2,2-dichloro-3-propyltristannane
                          13. Me 3 SnCH 2 CH 2 C CSnMe 3
                              but-1-yne-1,4-diylbis(trimethylstannane)


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