Efficient Protocol for the Synthesis of " N -Coded" Oligo- and Poly( N -Substituted Urethanes).
Tathagata MondalVincent GreffBenoît Éric PetitLaurence CharlesJean-François LutzPublished in: ACS macro letters (2019)
Sequence-defined poly( N -substituted urethanes) were synthesized via a solid-phase iterative protocol including two successive orthogonal coupling steps: the formation of an activated carbonate and its chemoselective reaction with the secondary amine group of amino alcohol building blocks. This simple method was used to write binary information on the formed polymers using four-coded molecules, 2-(methylamino)ethanol, 2-(ethylamino)ethanol, 2-(propylamino)ethanol, and 2-(butylamino)ethanol, symbolizing binary dyads 00, 01, 10, and 11, respectively. The method is fast and allows synthesis of uniform oligomers and polymers with controlled lengths (4-mer to 28-mer) and digital information sequences. Furthermore, the coded poly( N -substituted urethanes) were easily characterized by electrospray mass spectrometry and decoded by tandem mass spectrometry. Overall, these digital macromolecules offer interesting advantages over conventional sequence-coded polyurethanes, i.e., synthesis of longer chains, reduced synthesis times, and better solubility and processing in common organic solvents.
Keyphrases
- liquid chromatography
- mass spectrometry
- tandem mass spectrometry
- high performance liquid chromatography
- molecular docking
- gas chromatography
- randomized controlled trial
- ultra high performance liquid chromatography
- ionic liquid
- high resolution
- simultaneous determination
- high resolution mass spectrometry
- magnetic resonance imaging
- healthcare
- computed tomography
- amino acid
- solid phase extraction
- image quality