The Zn(II)-1,4,7-Trimethyl-1,4,7-Triazacyclononane Complex: A Monometallic Catalyst Active in Two Protonation States
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In this paper, the unusual reactivity of the complex Zn(II)-1,4,7-trimethyl-1, 4,7-triazacyclononane () in the transesterification of the RNA-model substrate, (), is reported. The dependence of the reactivity (k) with pH does not follow the characteristic bell-shape profile typical of complexes with penta-coordinated metal centers. By the contrary, two reactive species, featuring different deprotonation states, are present, with the tri-aqua complex being more reactive than the mono-hydroxy-diaqua one. Apparently, such a difference arises from the total complex charge which plays an important role in the stability of the transition state/s of the reactions. Relevant insight on the reaction mechanism were hence obtained.
Ueda H, Suzuki M, Kuroda R, Tanaka T, Aoki S J Med Chem. 2021; 64(12):8523-8544.
PMID: 34077212 PMC: 8279495. DOI: 10.1021/acs.jmedchem.1c00445.
Cleavage of an RNA Model Compound by an Arylmercury Complex.
Saleh L, Ora M, Lonnberg T Chembiochem. 2021; 22(10):1761-1764.
PMID: 33448598 PMC: 8247959. DOI: 10.1002/cbic.202000799.
Host-Guest Allosteric Control of an Artificial Phosphatase.
Czescik J, Lyu Y, Neuberg S, Scrimin P, Mancin F J Am Chem Soc. 2020; 142(15):6837-6841.
PMID: 32212681 PMC: 7997383. DOI: 10.1021/jacs.9b12699.