An expedient regioselectivesynthesis of novel mono, C₂-symmetric bis-triazole and acridinedione bridged macromolecules has been achieved in good yields employing intermolecular Cu(I) catalyzed azide and alkyne click reaction. Synthesis of O-propargyl acridinedione was achieved in three good yielding steps starting from dimedone, while the symmetrical aliphatic and aryl bis-azides were derived from appropriate dibromides in the presence of sodium azide in dry DMF. The synthesized mono and C₂-symmetric bis-macromolecules have been elucidated by ¹H, ¹³C, elemental and mass spectroscopic analysis. The antioxidant activity of synthesized compounds has also been investigated.

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利用分子间Cu（I）催化的叠氮化物和炔烃点击反应，以高收率实现了新型单，C ₂对称双三唑和a啶二酮桥联的大分子的区域选择性合成。从二甲酮开始，在三个良好的产率步骤中完成了O-炔丙基yl啶二酮的合成，而对称的脂族和芳基双叠氮化物是在干燥的DMF中，在叠氮化钠存在下，由适当的二溴化物衍生而来的。通过¹ H，¹³ C，元素和质谱分析已阐明了合成的单和C ₂对称双大分子。还研究了合成化合物的抗氧化活性。

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