Dendritic carbosilanes containing silicon-bonded 1-[C6H2(CH2NMe2)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

被引:46
|
作者
Kleij, AW
Kleijn, H
Jastrzebski, JTBH
Smeets, WJJ
Spek, AL
van Koten, G
机构
[1] Univ Utrecht, Dept Met Mediated Synth, Debye Inst, NL-3584 CH Utrecht, Netherlands
[2] Univ Utrecht, Dept Crystal & Struct Chem, Bijvoet Ctr Biomol Res, NL-3584 CH Utrecht, Netherlands
关键词
D O I
10.1021/om980627e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A useful synthetic procedure for the incorporation of the potentially multidentate 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 precursors [C6H3(CH2NMe2)(2)-3,5-Br-1], 1, and [C6H4(CH2NMe2)-4-Br-1], 2, in Et2O 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, which 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 [CH2SiMe2C6H2(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 their lithiated derivatives. In addition, the functionalized carbosilane dendrimers 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 compounds, can also be quantitatively converted into highly aggregated, polylithium derivatives. An X-ray molecular structure determination of 7 revealed this 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 centers 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.
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页码:268 / 276
页数:9
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