An Efficient Method for Covalent Surface Functionalization of Ultrasmall Metallic Nanoparticles by Surface Azidation Followed by Copper‐Catalyzed Azide‐Alkyne Cycloaddition (Click Chemistry)
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
An Efficient Method for Covalent Surface Functionalization of Ultrasmall Metallic Nanoparticles by Surface Azidation Followed by Copper‐Catalyzed Azide‐Alkyne Cycloaddition (Click Chemistry) ; day:08 ; month:11 ; year:2021 ; extent:1
ChemNanoMat ; (08.11.2021) (gesamt 1)
- Creator
- DOI
-
10.1002/cnma.202100359
- URN
-
urn:nbn:de:101:1-2021110814175409218122
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Klein, Kai
- Loza, Kateryna
- Heggen, Marc
- Epple, Matthias
Other Objects (12)
Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition
Efficient catenane synthesis by cucurbit[6]uril-mediated azide–alkyne cycloaddition
All Sugar Based Cellulose Derivatives Synthesized by Azide–Alkyne Click Chemistry
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Highly active dinuclear copper catalysts for homogeneous azide-alkyne cycloadditions
Highly Active Dinuclear Copper Catalysts for Homogeneous Azide-Alkyne Cycloadditions
Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst
Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst
Chemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide Cycloadditions
Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition
Efficient catenane synthesis by cucurbit[6]uril-mediated azide–alkyne cycloaddition
All Sugar Based Cellulose Derivatives Synthesized by Azide–Alkyne Click Chemistry
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Highly active dinuclear copper catalysts for homogeneous azide-alkyne cycloadditions
Highly Active Dinuclear Copper Catalysts for Homogeneous Azide-Alkyne Cycloadditions
Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst
Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst
Chemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide Cycloadditions
Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition
Efficient catenane synthesis by cucurbit[6]uril-mediated azide–alkyne cycloaddition
All Sugar Based Cellulose Derivatives Synthesized by Azide–Alkyne Click Chemistry
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Highly active dinuclear copper catalysts for homogeneous azide-alkyne cycloadditions
Highly Active Dinuclear Copper Catalysts for Homogeneous Azide-Alkyne Cycloadditions
Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst
Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst