Evidence map›Paper›PMID 42479475›Full record

ArticleAccounts of chemical research2026

Rational Design of Supramolecular Fe and Mn Oxidation Catalysts.

Giorgio Olivo, Miquel Costas, Stefano Di Stefano

Abstract read
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Article in Accounts of chemical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Giorgio OlivoDipartimento di Chimica and Istituto CNR per i Sistemi Biologici (ISB-CNR), Sezione Meccanismi di Reazione, c/o Dipartimento di Chimica Università di Roma "La Sapienza", P.le A.Moro 5, I-00185Rome, Italy.ORCID 0000-0003-4053-7673
Miquel CostasDepartament de Quimica Universitat de Girona Campus Montilivi, QBIS-Cat, Institut de Química Computacional i Catàlisi (IQCC), 17071Girona, Catalonia, Spain.ORCID 0000-0001-6326-8299
Stefano Di StefanoDipartimento di Chimica and Istituto CNR per i Sistemi Biologici (ISB-CNR), Sezione Meccanismi di Reazione, c/o Dipartimento di Chimica Università di Roma "La Sapienza", P.le A.Moro 5, I-00185Rome, Italy.ORCID 0000-0002-6742-0988

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modern organic synthesis aims to prepare the target molecule in a minimal number of steps. Hence, the efficiency, selectivity, and predictability of each of these steps need to be carefully optimized, even at a late stage of a synthetic route. This is particularly true in the case of aliphatic C-H functionalization, since differentiating one C-H bond among many others with similar properties in organic molecules often stands as an open challenge. Remote, inactivated C-H sites are especially difficult to target. Supramolecular catalysis represents one of the tools to overcome such problems. As occurs in enzymes, substrate binding to a supramolecular catalyst constrains their relative orientation, and the resulting preorganization can increase reactivity and unlock unusual selectivity in a rational and predictable manner, meeting late-stage functionalization requirements. In fact, supramolecular catalysis, which was initially oriented to the comprehension of the mechanisms of the involved reactions, is currently and rapidly evolving into a synthetically useful tool. One decade ago, in 2017, we described Fe- and Mn-based supramolecular catalysts equipped with crown ether recognition sites able to efficiently catalyze the oxidation of inactivated C-H bonds in protonated primary amines. Substrate preorganization induced by recognition enables elusive oxidation at remote C8 and C9 sites in linear alkyl chains. Since then, a number of follow-up investigations allowed us to rationally elicit unnatural reactivity and selectivity in different bioinspired oxidation reactions, including predictable, late-stage C-H oxidation of steroids. In addition, an in-depth analysis of such oxidation processes provides a deep comprehension of the action mechanism of these supramolecular catalysts. In this Account, we discuss the above investigations aiming to show (i) the rational approach to the design of a supramolecular oxidation catalyst, (ii) the experimental and theoretical tools that help understand and assess its mechanism of action, and (iii) its potential to address synthetic challenges. Eventually, a section that compares our approach to the one of other research groups illustrates the state of the art in supramolecular oxidation catalysis.

Identifiers

PMID42479475
PMCPMC13445584

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