Some scientific research about Tris(2-pyridylmethyl)amine

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Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 16858-01-8, molcular formula is C18H18N4, introducing its new discovery. Application In Synthesis of Tris(2-pyridylmethyl)amine

Three new morpholine-based ligands were synthesized to better control ATRP in aqueous media. 4-(bis(N,N-diethylaminoethyl)aminoethyl)morpholine (MMA), N,N-diethylaminoethyl-bis(2-morpholinoethyl)amine, and tris(2-morpholinoethyl)amine ligands were created and investigated to better understand the effect of electron withdrawing groups on the degree of control obtained under aqueous ATRP conditions. Polymerization performance of these ligands with the neutral oligo(ethylene glycol) methyl ether methacrylate and zwitterionic carboxybetaine methacrylate monomers was compared with tris(2-(diethylamino)ethyl)amine (Et6TREN) ligand. The new ligands showed decreased polymerization rates and yielded polymers with lower dispersities than those synthesized with Et6TREN. These results indicated that altering the basicity of the central tertiary amine is an important factor in controlling the stability of the copper(I) complex, leading to better control over aqueous ATRP. Finally, uniform protein?polymer conjugates were synthesized with the MMA ligand using protein-ATRP.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI