首页> 外文期刊>Crystal Structure Theory and Applications >Synthesis and Crystal Structure Determination of 4’,9’,4”,9”-Tetra-t-Butyl- 1’,6’,1”,6”-Tetramethoxy-2,5-Dithia[3.3] Metabiphenylophane
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Synthesis and Crystal Structure Determination of 4’,9’,4”,9”-Tetra-t-Butyl- 1’,6’,1”,6”-Tetramethoxy-2,5-Dithia[3.3] Metabiphenylophane

机译:4',9',4”,9''-四叔丁基-1',6',1”,6”-四甲氧基-2,5-二硫[3.3]偏二苯并菲烷的合成及晶体结构测定

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摘要

The title compound 4’,9’,4”,9”-tetra-tert-butyl-1’,6’,1”,6”-tetramethoxy-2,5-dithia[3.3] metabiphenylophane was synthesized as a calixarene like large-sized metacyclophane from the corresponding 3,3’-bis(chloromethyl)-5,5’-bis(1,1-dimethylethyl)-2,2’-dimethoxy-1,1’-biphenyl and 3,3’-bis (mercaptomethyl)-5,5’-bis(1,1-dimethylethyl)-2,2’-dimethoxy-1,1’-biphenyl via an intermolecular condensation reaction. The compound was characterized using 1H NMR spectroscopy and mass spectrometry. Its exact conformational structure was determined via single crystal X-ray diffraction analysis. The compound has quite strained 1,2-alternate like structure because of its two high dihedral angled and rigid biphenyl parts in the crystal. The crystal includes the two isomers as two different 1,2-alternate like conformers, and the ratio of the two isomers is 78:22.
机译:标题化合物4',9',4“,9”-四叔丁基-1',6',1“,6”-四甲氧基-2,5-二硫[3.3]间联苯苯并[8]相应的3,3'-双(氯甲基)-5,5'-双(1,1-二甲基乙基)-2,2'-二甲氧基-1,1'-联苯和3,3'-经由分子间缩合反应的双(巯基甲基)-5,5'-双(1,1-二甲基乙基)-2,2'-二甲氧基-1,1'-联苯。使用1H NMR光谱和质谱对化合物进行表征。通过单晶X射线衍射分析确定其确切的构象结构。该化合物由于在晶体中具有两个高的二面角和刚性联苯部分,因此具有非常紧张的1,2-交替结构。晶体包括作为两种不同的1,2-交替构象异构体的两种异构体,并且两种异构体的比例为78:22。

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