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Charles H. Devillers

Researcher at University of Burgundy

Publications -  78
Citations -  1137

Charles H. Devillers is an academic researcher from University of Burgundy. The author has contributed to research in topics: Porphyrin & Catalysis. The author has an hindex of 17, co-authored 76 publications receiving 961 citations. Previous affiliations of Charles H. Devillers include University of Tübingen & Centre national de la recherche scientifique.

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Ferrocene-appended porphyrins: Syntheses and properties

TL;DR: In this article, a review article focuses on the syntheses and potential applications of ferrocene-appended porphyrin architectures, including the connection at a meso position through a direct linkage, a conjugated or saturated spacer or using a non-covalent approach.
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Aromatic Nucleophilic Substitution (SNAr) of meso-Nitroporphyrin with Azide and Amines as an Alternative Metal Catalyst Free Synthetic Approach To Obtain meso-N-Substituted Porphyrins

TL;DR: Aromatic nucleophilic substitution reaction of the nitro group of meso-nitroporphyrins with azide and various amines was achieved and represents an alternative procedure to C-N coupling reactions usually needed to obtain such mese-N-substituted porphyrin in good yields.
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Magnesium(II) polyporphine: The first electron-conducting polymer with directly linked unsubstituted porphyrin units obtained by electrooxidation at a very low potential

TL;DR: In this paper, it was shown that the polymer film is composed by chains of Mg porphine building blocks, with single bonds between the neighboring units in the course of the potential sweep.
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BODIPY–diketopyrrolopyrrole–porphyrin conjugate small molecules for use in bulk heterojunction solar cells

TL;DR: In this paper, two small molecules denoted as BD-pPor and BD-tPor composed of a central BODIPY core surrounded with two DPP and two porphyrin units have been designed and synthesized.
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Long-range electronic connection in picket-fence like ferrocene–porphyrin derivatives

TL;DR: The effects of a direct connection between ferrocene and porphyrin units have been thoroughly investigated by electrochemical and spectroscopic methods and these data clearly demonstrate that the metallocene centres are "connected" through the p Morphyrin-based electronic network.