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Synthesis and spectral properties of axially bromo-substituted subphthalocyanines for optical storage

机译:轴向溴取代的亚酞菁用于光学储存的合成及光谱性能

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Subphthalocyanines (SubPc) are composed of three isoindole units containing boron inside, which defines a molecular axis and forms a coneshaped structure. Despite being non-planar, they show a delocalized 14 pi-electron system similar to that present in phthalocyanines. The attractive characterisktics of SubPc are their chemical stability and thermal stability. We report here the synthesis of three SubPc compounds, in which the axial substituent is a bromide. The peripheral substituent in the compounds leads to an improved solubility in common organic solvents. The results demonstrated that SubPc showed a strong and broad absorption region near 600 nm, This is advantageous for the purification and important for the applications in optical storage (DVD-R).
机译:甲酞菁(SubPC)由含有硼内部的三个异吲哚单元组成,其限定了分子轴并形成圆锥结构。尽管是非平面的,但它们显示了与酞菁中存在的临近14个PI-Electron系统。 Subpc的有吸引力的特征是它们的化学稳定性和热稳定性。我们在此报告三种子PC化合物的合成,其中轴向取代基是溴化物。化合物中的外周取代基导致普通有机溶剂中的溶解度提高。结果表明,Subpc在600nm附近显示出强烈宽的吸收区域,这对于纯化和对光学存储器(DVD-R)的应用是有利的。

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