Photoresponsive peptoid oligomers bearing azobenzene side chains
Organic & Biomolecular Chemistry2008Vol. 6(14), pp. 2516–2516
Citations Over TimeTop 23% of 2008 papers
Abstract
N-Substituted glycine peptoid oligomers were synthesized to incorporate a photoresponsive azobenzene side chain. The ability of this side chain to undergo reversible photoisomerization was established, and the cis- to trans-azobenzene thermal isomerization of this side chain was investigated. Circular dichroism studies indicated that trans- to cis-azobenzene isomerization does not significantly alter the backbone conformation in a series of peptoids thought to have well-defined structures.
Related Papers
- → Pseudopolyrotaxane composed of an azobenzene polymer and γ-cyclodextrin. Reversible and irreversible photoisomerization of the azobenzene groups in the polymer chain(2000)19 cited
- → Synthesis and photoisomerization of an azobenzene derivative bearing two -cyclodextrin units at both ends(1998)15 cited
- → Photoisomerization Behavior of Smectic Liquid Crystalline AZO Polymers(2001)5 cited
- → Efficient Photoisomerization of Hybrid Langmuir-Blodgett Films of Amphiphilie Anionic Azobenzene and Alkylammonium with Long Alkyl Chains(2004)1 cited
- → Photoisomerization of Azobenzene Derivatives at the Air/Water Interface(2000)