4.8 Article

A Ligand System for the Flexible Functionalization of Quantum Dots via Click Chemistry

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 57, 期 17, 页码 4652-4656

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201801113

关键词

capping ligand; cell labeling; click chemistry; quantum dots; surface modification

资金

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Materials Science and Engineering [DE-FG02-07ER46454]
  2. U.S. Army Research Office through the Institute for Soldier Nanotechnologies [W911NF-13-D-0001]
  3. U.S. National Science Foundation [ECCS-1449291]
  4. MIT Deshpande Center Innovation Grant
  5. Boehringer Ingelheim Fonds
  6. National Science Foundation [DMR-14-19807]
  7. Directorate For Engineering [1449291] Funding Source: National Science Foundation

向作者/读者索取更多资源

We present a novel ligand, 5-norbornene-2-nonanoic acid, which can be directly added during established quantum dot (QD) syntheses in organic solvents to generate clickable QDs at a few hundred nmol scale. This ligand has a carboxyl group at one terminus to bind to the surface of QDs and a norbornene group at the opposite end that enables straightforward phase transfer of QDs into aqueous solutions via efficient norbornene/tetrazine click chemistry. Our ligand system removes the traditional ligand-exchange step and can produce water-soluble QDs with a high quantum yield and a small hydrodynamic diameter of approximately 12 nm at an order of magnitude higher scale than previous methods. We demonstrate the effectiveness of our approach by incubating azido-functionalized CdSe/CdS QDs with 4T1 cancer cells that are metabolically labeled with a dibenzocyclooctyne-bearing unnatural sugar. The QDs exhibit high targeting efficiency and minimal nonspecific binding.

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