化学
部分
晶体结构
分子间力
结晶学
试剂
单晶
红外光谱学
核磁共振波谱
配位复合体
立体化学
分子
有机化学
金属
作者
Thomas M. Klapötke,Burkhard Krumm,M. Scherr
标识
DOI:10.1002/ejic.200800565
摘要
Abstract The syntheses of the triorganochalcogenium dinitramide salts [Ph 3 Te][N(NO 2 ) 2 ] ( 1 ), [Me 3 Te][N(NO 2 ) 2 ] ( 2 ), [Ph 3 Se][N(NO 2 ) 2 ] ( 3 ), [Me 3 Se][N(NO 2 ) 2 ] ( 4 ), [Ph 3 S][N(NO 2 ) 2 ] ( 5 ), and [Me 3 S][N(NO 2 ) 2 ] ( 6 ), their characterization by multinuclear NMR spectroscopy, vibrational spectra, and single‐crystal structures are described. The syntheses of the compounds were achieved with the help of [Ag(py) 2 ][N(NO 2 ) 2 ] and [Ag(NCCH 3 )][N(NO 2 ) 2 ] as dinitramide transfer reagents. Whereas in the crystal structure of 1 different coordination modes to dinitramide moieties are present, the crystal structure of 3 shows only a single intermolecular contact to the dinitramide moiety. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
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