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Issue 7, 2015
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Stable iso-bacteriochlorin mimics from porpholactone: effect of a β-oxazolone moiety on the frontier π-molecular orbitals

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Abstract

Iso-bacteriochlorins known as siroheme in some reductases, featured with two adjacent reduced pyrrole rings, have distinctive electronic structures from porphyrin, chlorin and bacteriochlorin analogues. However, the synthesis of such cofactor mimics from hydrogenation of chlorin or porphyrin is associated with drawbacks of uncertain regioselectivity and stability. In this work, we present the first example of selective hydrogenation of the adjacent pyrroles in porphyrin or porpholactone free bases assisted by the Woollins reagent (WR). More importantly, adjacent-dihydroporpholactone (1a) displays iso-bacteriochlorin type spectral features and much higher stability under oxidative conditions, compared to the tetrahydroporphyrin analogue (2a). Analysis of magnetic circular dichroism (MCD) spectra and DFT calculations for the frontier π-molecular orbitals for 1a and 2a reveals the significant effect of a β-oxazolone moiety replacement on lowering the HOMO energy level and enhancing the stability resistant to oxidative conditions.

Graphical abstract: Stable iso-bacteriochlorin mimics from porpholactone: effect of a β-oxazolone moiety on the frontier π-molecular orbitals

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Publication details

The article was received on 31 Mar 2015, accepted on 12 Jun 2015 and first published on 12 Jun 2015


Article type: Research Article
DOI: 10.1039/C5QI00054H
Author version available: Download Author version (PDF)
Citation: Inorg. Chem. Front., 2015,2, 671-677
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    Stable iso-bacteriochlorin mimics from porpholactone: effect of a β-oxazolone moiety on the frontier π-molecular orbitals

    Y. Yu, T. Furuyama, J. Tang, Z. Wu, J. Chen, N. Kobayashi and J. Zhang, Inorg. Chem. Front., 2015, 2, 671
    DOI: 10.1039/C5QI00054H

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