On-Surface Azide–Alkyne Cycloaddition on Au(111)
✍ Scribed by Díaz Arado, Oscar; Mönig, Harry; Wagner, Hendrik; Franke, Jörn-Holger; Langewisch, Gernot; Held, Philipp Alexander; Studer, Armido; Fuchs, Harald
- Book ID
- 121329683
- Publisher
- American Chemical Society
- Year
- 2013
- Tongue
- English
- Weight
- 905 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1936-0851
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## Abstract Organomicelles modified by surface dibenzylcyclooctyne moieties can conveniently be functionalized by strain‐promoted alkyne–azide cycloadditions. The ligation approach is highly efficient, does not require toxic reagents and is compatible with a wide variety of functional modules. Inte
## Abstract __N__‐substituted glycine oligomers, or peptoids, can be used in conjunction with the copper‐catalyzed [3 + 2] cycloaddition of azides and alkynes to generate branched polymer networks. By incorporating both azides and alkynes as side chain functionalities on the oligomer scaffolds, pep