| Agency: | ENERGY, DEPARTMENT OF |
|---|---|
| State: | New Mexico |
| Type of Government: | Federal |
| FSC Category: |
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| NAICS Category: |
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| Set Aside: | No Set aside used |
| Posted Date: | May 12, 2026 |
| Due Date: | Jun 30, 2026 |
| Solicitation No: | S-133639 |
| Original Source: | Please Login to View Page |
| Contact information: | Please Login to View Page |
| Bid Documents: | Please Login to View Page |
Peptoid-based chelating ligands offer a tunable platform for capturing and holding specific metal ions with high selectivity while resisting breakdown under physiological conditions. The technology combines structural flexibility with strong binding performance, which creates a practical path for applications where existing chelators fall short, including difficult metal removal in biological, environmental and separation settings.
How it Works
Peptoid-Based Chelating Ligands uses cyclic peptoid scaffolds, which are peptoid chains closed into ring structures and decorated with side chains chosen for metal binding. By changing the ring size, side-chain chemistry and spacing between binding groups, the ligand can be adjusted to favor certain hard metal ions, especially actinides and lanthanides.
Technical Description
Peptoids differ from peptides because their side chains attach to nitrogen rather than to carbon, which makes them more resistant to hydrolysis under physiological conditions. That stability matters because many conventional chelators can lose activity in the body or in harsh process streams, while peptoid-based structures are designed to remain intact long enough to bind and hold the target metal.
The invention describes cyclic peptoid ligands that can be built from linear peptoids and then cyclized, with the binding profile tuned through functional groups such as catecholates, phosphonates, amines, guanidinium groups, phosphoramidates, N-hydroxypyridones and CMPO-like groups. Linker length, hydrophobicity, hydrophilicity and the number of coordinating groups can be adjusted to improve selectivity for specific ions and to support either tight retention for removal or controlled release after capture.
Advantages
Market Applications
TRL 4
US Patent Nos. 11,254,708; 11,859,018
LA-UR-26-23913
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