期刊
CHEMICAL COMMUNICATIONS
卷 51, 期 23, 页码 4846-4849出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc00518c
关键词
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资金
- MIUR [PRIN 20109Z2XRJ_010]
A reactive azlactone-based graphene nanoplatform was successfully synthesized by the ligation of azido-azlactone with alkyne-terminated graphene via Cu(I)-catalyzed cycloaddition. The reactive azlactone rings, grafted on graphene sheets, were subjected to highly efficient ring-opening reactions with functionalized primary amine derivatives incorporating an aminosilane coupling agent or a biological fragment.
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