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A Short Bi=Bi Bond Supported by a Metalloid Group 13 Ligand

机译:由准金属13号配体支撑的短Bi = Bi键

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Multiple bonds between main-group metals have brought much attention for more than the last two decades owing to both inherent fundamental chemistry and applications in synthesis. Particularly the isolation and structural characterization of multiply bonded Group 15 elements has posed a challenge to synthetic chemists. The first structurally characterized compound with a bismuth-bismuth double bond was discovered by Tokitoh et al. in 1997; it was prepared by treating sterically crowded tbtBiCl2 (tbt = 2,4,6-[(Me3Si)2CH]3C6H2) with Li2Se and subsequent reduction of resulting (tbtBiSe)3 with three equivalents of (Me2N)3P. Subsequently, it was shown that RBi=BiR (R = 2,6-(2,4,6-Me3C6H2)2C6H3 or bbt, 4-(SiMe3)3C-2,6-[(Me3Si)2CH]2C6H2) can also be obtained by the controlled reduction of the corresponding monoorganyl bismuth dihalides with magne-sium.
机译:由于固有的基本化学性质和在合成中的应用,近二十年来,主族金属之间的多重键引起了人们的极大关注。特别是多重键合的15族元素的分离和结构表征对合成化学家提出了挑战。 Tokitoh等人发现了第一个具有铋-铋双键的结构特征化合物。 1997年;通过用Li2Se处理空间上拥挤的tbtBiCl2(tbt = 2,4,6-[(Me3Si)2CH] 3C6H2),然后用三当量的(Me2N)3P还原生成的(tbtBiSe)3来制备。随后表明,RBi = BiR(R = 2,6-(2,4,6-Me3C6H2)2C6H3或bbt,4-(SiMe3)3C-2,6-[(Me3Si)2CH] 2C6H2)也可以通过用镁可控地还原相应的一有机基二卤化铋可得到。

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