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Nidal Saleh

Researcher at University of Rennes

Publications -  29
Citations -  935

Nidal Saleh is an academic researcher from University of Rennes. The author has contributed to research in topics: Helicene & Phosphine. The author has an hindex of 15, co-authored 29 publications receiving 730 citations. Previous affiliations of Nidal Saleh include Centre national de la recherche scientifique & Institut de Chimie des Substances Naturelles.

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Helicene-based transition metal complexes: synthesis, properties and applications

TL;DR: The coordination and/or organometallic chemistry of π-helicenic ligands is a powerful tool to generate multifunctional molecules displaying optimized chiroptical properties combined with new properties furnished by the metallic center.
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Acid/Base‐Triggered Switching of Circularly Polarized Luminescence and Electronic Circular Dichroism in Organic and Organometallic Helicenes

TL;DR: The very large bathochromic shift of the emission observed upon protonation of azahelicene-bipyridine 1 a has been attributed to the decrease in aromaticity (promoting a charge-transfer-type transition rather than a π-π* transition) as well as an increase in the HOMO-LUMO character of the transition and stabilization of the LUMO level upon proptonation.
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enantio-Enriched CPL-active helicene–bipyridine–rhenium complexes

TL;DR: The incorporation of a rhenium atom within an extended helical π-conjugated bi-pyridine system impacts the chiroptical and photophysical properties of the resulting neutral or cationic complexes as discussed by the authors.
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Synthesis of 9H-Pyrrolo[1,2-a]indole and 3H-Pyrrolizine Derivatives via a Phosphine-Catalyzed Umpolung Addition/Intramolecular Wittig Reaction

TL;DR: The first umpolung addition/intramolecular Wittig reaction, catalytic in phosphine, is described and is applicable to the synthesis of a wide range of functionalized 9H-pyrrolo[1,2-a]indoles and pyrrolizines.
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From phosphine-promoted to phosphine-catalyzed reactions by in situ phosphine oxide reduction

TL;DR: In this paper, the regeneration of the active catalyst was possible by means of reagents that reduce in situ the phosphine oxide formed during the reaction, and the results on newly developed phosphine-catalyzed reactions were summarized.