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Updated: Jun 6, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Immobilized CuO hollow nanospheres catalyzed alkyne-azide cycloadditions
Hyuntae Kang1, Hyun Seok Jung, Jee Young Kim
1Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University, Busan 609-735, Korea.
Abstract:
An approach for gram-scale synthesis of uniform Cu2O nanocubes by a one-pot polyol process was used. The CuO hollow nanostructures were prepared by adding aqueous ammonia solutions with Cu2O nanocube colloidal solutions. CuO hollow nanospheres on acetylene black (CuO/AB), were synthesized and used for the catalytic [3+2] cycloaddition of azides with terminal alkynes to provide products in good yields with high regioselectivity. The CuO/AB was readily separated by centrifugation and could be reused ten times under the present reaction conditions without any loss of catalytic activity. Transition metals loaded onto acetylene black are useful reagents for a wide variety of organic transformations. Moreover, these heterogeneous systems are promising industrial catalysts.
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