A Kharash-type Grignard cross-coupling reaction of phenyl-d5-magnesium bromide and an appropriate diiodo compound in the presence of bis (acetylacetonato) nickel (II) was successfully employed for the syntheses of twelve new decadeuterated polyphenyls, each of which has phenyl-d5 rings at both termini. On the basis of the nuclear magnetic resonance spectra of the deuterated and normal polyphenyls, close correlations between the apparent signal patterns of phenylene groups and the structures of the adjacent groups became apparent. The mass spectral studies revealed that the deuterated polyphenyls containing o-linkage (s) were less stable to electron bombardment than those containing no o-linkage. Inspection of the ultraviolet spectra of the deuterated polyphenyls showed that the isotope effect in their K-bands was hardly detectable.
在双(
乙酰丙酮)
镍(II)存在下,苯基-d5-
溴化镁和适当的二
碘化合物的卡拉什型格氏交叉偶联反应成功地用于合成十二种新的十
氘代多苯基,每种都含有苯基-d5 在两个末端均响铃。根据
氘代和正态聚苯的核磁共振谱,亚苯基的表观信号模式与相邻基团的结构之间的密切相关性变得明显。质谱研究表明,含有o-键的
氘代多苯对电子轰击的稳定性低于不含o-键的
氘代多苯。对
氘代聚苯的紫外光谱的检查表明,其K带中的同位素效应几乎检测不到。