REACTIONS OF TETRAKIS[BIS(TRIMETHYLSILYL) METHYL]DIALANE(4) WITH METHYLISOTHIOCYANATE AND PHENYLISOCYANATE - INSERTION INTO THE AL-AL BOND AND FRAGMENTATION
W. Uhl et al., REACTIONS OF TETRAKIS[BIS(TRIMETHYLSILYL) METHYL]DIALANE(4) WITH METHYLISOTHIOCYANATE AND PHENYLISOCYANATE - INSERTION INTO THE AL-AL BOND AND FRAGMENTATION, Zeitschrift fur anorganische und allgemeine Chemie, 622(2), 1996, pp. 373-379
Citations number
32
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Zeitschrift fur anorganische und allgemeine Chemie
Tetrakis[bis(trimethylsilyl)methyl]dialane(4) 1 reacts with methyl iso
thiocyanate under cleavage of the C=S double bond and insertion of the
remaining isonitrile fragment into the Al-Al bond. As shown by crysta
l structure determination a three-membered AlCN heterocycle (4) is for
med by the interaction of the nitrogen lone pair with one unsaturated
Al atom leading to an acute angle at the aluminium center N-Al-C of 36
.6 degrees. In contrast the reaction with the hard base phenyl isocyan
ate yields a mixture of many unknown compounds, from which only one (5
) could be isolated in a very poor yield. The crystal structure of 5 r
eveals only one dialkyl aluminium fragment and a chelating ligand form
ed by the trimerization of the isocyanate under loss of one CO group a
nd addition of a hydrogen atom. 5 was also synthesized by the specific
reaction of the chloro dialkyl aluminium compound (R=CH(SiMe(3))(2))
with Li[H5C6-N=C(O)-N(C6H5)-C(O)-N(H)-C6H5].