Dendritic carbosilanes containing silicon-bonded 1-[C6H2(CH(2)NM(e)2)(2)-3,5-Li-4] or 1-[C6H3(CH2NMe2)-4-Li-3] mono and bis(amino)aryllithium end groups: Structure of {[CH2SiMe2C6H3(CH2NMe2)-4-Li-3](2)}(2)

A useful synthetic procedure for the incorporation of the potentially multi dentate monoanionic 1-[C6H2(CH2NMe2)(2)-3,5](-) (=NCN) and 1-[C6H3(CH2NMe2) -4](-) (=CN) ligands via the para-position on the periphery of carbosilane (CS) dendrimers has been developed. Lithiation of suitable brominated precu rsors [C6H3(CH2NMe2)(2)-3,5-Br-1], 1, and [C6H4(CH2NMe2)-4-Br-1], 2, in Et2 O at -78 degrees C with 2 equiv of t-BuLi gives the monolithiated aminoaryl compounds Li[C6H3(CH2NMe2)(2)-3,5], 1-Li, and Li[C6H4(CH2NMe2)-4], 2-Li, w hich can be subsequently treated in situ with the silicon chlorides ClSiMe2 (CH2)(n)SiMe2Cl (n = 2 or 6) to yield the functionalized CS-ligand systems [CH2SiMe2C6H3(CH2NMe2)(2)-3,5](2), 3, and [(CH2)(n)SiMe2C6H4(CH2NMe2)-4](2) (for 4, n = 1; for 5, n = 3). The ligand systems 3-5 react with 2 equiv of t-BuLi to give the dilithiated derivatized carbosilane molecules [CH2SiMe2 C6H2(CH2NMe2)(2)-3,5-Li-4](2) and [(CH2)(n)SiMe2C6H4(CH2NMe2)-4-Li-3](2) (7 , n = 1) in good chemical yields. Quench reactions of the in situ prepared lithiated derivatives with either D2O, Me3SiCl/Me3SiOTf, or MeSSMe clearly showed that the CS-ligand systems have been quantitatively converted into t heir lithiated derivatives. In addition, the functionalized carbosilane den drimers G0-SiMe2-(N)CN and G1-SiMe2-(N)CN (13-16), which can be prepared in high yield by using the same synthetic approach used for the model compoun ds, can also be quantitatively converted into highly aggregated, polylithiu m derivatives. An X-ray molecular structure determination of 7 revealed thi s compound to be a unique dimeric aggregate {[CH2SiMe2C6H3(CH2NMe2)-4-Li-3] (2)}(2) with their respective 2-electron-4-center (4c-2e) anionic C-ipso ce nters each bonded to a Li-3 face. As a result the (Me)(2)SiCH2CH2Si(Me)(2) CS backbone exhibits a nonideal trans conformation with a vicinal dihedral angle of -161 degrees.