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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >Reactivity of 2,6‐Dihalophenyl Lithium Reagents Towards Chlorosilanes. Synthesis and Structure of 2,3‐ and 2,6‐Dihalophenyl(di‐)silanes
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Reactivity of 2,6‐Dihalophenyl Lithium Reagents Towards Chlorosilanes. Synthesis and Structure of 2,3‐ and 2,6‐Dihalophenyl(di‐)silanes

机译:2,6二卤苯基锂试剂对氯硅烷的反应性。 2,3-和2,6二卤代苯基(二溴苯基(DI-)硅烷的合成和结构

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摘要

> The reaction of 2,6‐dihalophenyllithium 2,6‐ X 2 C 6 H 3 Li ( X = F, Cl, Br) with the chlorosilanes ClMe 2 SiSiCl 2 Me, SiCl 4 , and HSiCl 3 afforded the diaryldisilanes (2,6‐ X 2 C 6 H 3 SiMe 2 ) 2 [ X = F ( 1a ), Cl ( 1b ), Br ( 1c )] and the diaryl‐ and triarylsilanes (2,6‐ X 2 C 6 H 3 ) 2 SiCl 2 [ X = F ( 3a ), Cl ( 3a )], (2,3‐Br 2 C 6 H 3 ) 2 SiCl 2 ( 4c ), (2,6‐F 2 C 6 H 3 ) 3 SiH ( 6a ), and (2,6‐ X 2 C 6 H 3 ) 2 Si(H)Cl [ X = Cl ( 7b ), Br ( 7c )], respectively. The formation of 4c was rationalized on the basis of an equilibrium that exists between the aryllithium isomers 2,6‐Br 2 C 6 H
机译: > 2,6-二卤苯基锂的反应2,6-二卤蛋白2,6- x 2 c 6 h <亚> 3 Li( x = F,Cl,Br),用氯硅烷Clme 2 sisicl 2 me,siCl 4 ,HSICL 3 提供了二芳基硅烷(2,6- x 2 c 6 h 3 sime 2 2 [ x = f( 1a ),cl ( 1b ),Br( 1c )]和二芳基和三芳基硅烷(2,6- x 2 C 6 h 3 2 siCl 2 [ x = f( 3a ),cl( 3a )],(2,3-br 2 C 6 h 3 2 siCl 2 ( 4c ),(2, 6-F 2 c 6 h 3 3 sih( 6a ), (2,6- x 2 c 6 h 3 2 si (H)CL [ x = CL( 7b ),分别为BR( 7c )]。 4c 的形成是基于芳基异构体2,6-Br 2 / sex> c 6 h之间存在的平衡来合理化的。

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