Jad Rabah

ORCID: 0000-0001-7301-8082
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About
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Research Areas
  • Luminescence and Fluorescent Materials
  • Fullerene Chemistry and Applications
  • Porphyrin and Phthalocyanine Chemistry
  • Molecular Junctions and Nanostructures
  • Molecular Sensors and Ion Detection
  • Photochemistry and Electron Transfer Studies
  • Organic Electronics and Photovoltaics
  • Advanced biosensing and bioanalysis techniques
  • Conducting polymers and applications
  • Polydiacetylene-based materials and applications
  • Graphene research and applications
  • Carbon and Quantum Dots Applications
  • Supramolecular Self-Assembly in Materials
  • Dyeing and Modifying Textile Fibers
  • Organic Light-Emitting Diodes Research

Institut Lavoisier de Versailles
2020-2024

Université de Versailles Saint-Quentin-en-Yvelines
2018-2024

Centre National de la Recherche Scientifique
2018-2024

Université Paris-Saclay
2020-2024

Molina Center for Energy and the Environment
2023

Université de Rennes
2019

Abstract Two BODIPY‐C 60 ‐peptide assemblies were synthesized by CuAAC reactions of dyads and a helical peptide functionalized with terminal alkyne group an azide group, respectively. The within these was at its other end disulfide allowing formation self‐assembled monolayers (SAMs) on gold surfaces. Characterizations SAMs, as well those reference molecules (BODIPY‐C ‐alkyl, C BODIPY‐peptide), carried out PM‐IRRAS cyclic voltammetry. SAMs are more densely packed than ‐alkyl BODIPY‐peptide...

10.1002/cplu.202300717 article EN cc-by ChemPlusChem 2024-02-26

A new donor-acceptor dyad composed of a BODIPY (4,4'-difluoro-4-bora-3a,4a-diaza-s-indacene) donor and fullerene C60 acceptor has been synthesized characterized. This derivative prepared using clickable building block that bears an alkyne moiety maleimide unit. The post-functionalization the group by thiol leads to BODIPY-C60 dyad, leaving for further functional arrangement. On basis combination semi-empirical density theory (DFT) calculations, spectroelectrochemical experiments,...

10.1021/acs.jpcb.0c05187 article EN The Journal of Physical Chemistry B 2020-09-08

A borondipyrromethene (BODIPY)–ferrocene dyad where both units are connected by an ethynylstyryl linker was synthesized, and its fluorescence electrochemical electrofluorochromic features were analyzed first in solution then as a surface-confined species. Immobilization achieved siloxane derivatization at the meso position of BODIPY, which enabled covalent grafting onto ITO surface. The resulting monolayer showed high stability redox response positive electrofluorochromism. Fluorescent...

10.1021/acs.jpcc.4c03441 article EN The Journal of Physical Chemistry C 2024-09-02

Abstract A straightforward synthesis of molecular gelators [1][C n Bn] and [1][bisC (n=12, 16) based on ionic interactions between Aggregation‐Induced Emission (AIE)‐active anionic phosphole functionalized imidazolium [C [bisC is described. These new can form luminescent organogels in various solvents. The fibers were characterized by laser scanning confocal microscopy. Also, a 30‐fold increase luminescence quantum yield was observed the diluted solution (0.6 %) xerogel (20 12 , thus...

10.1002/cplu.201900584 article EN ChemPlusChem 2019-11-22

A helical <bold>C60-peptide</bold> allowed the formation of well-packed SAMs compared to a <bold>C60-alkyl</bold> peptide, which was determined by QCM and CV experiments.

10.1039/c8nj04599b article EN New Journal of Chemistry 2018-01-01

Abstract Ferrocene‐BODIPY (Fc‐BDP) conjugates in which one or two ferrocene entities are linked to the β‐positions of BODIPY core by an ethynyl bridge have been developed. These derivatives were easily and efficiently grafted onto a dual‐clickable fullerene platform using CuAAC reactions, leading clickable Fc‐BDP‐C 60 triad [Fc] 2 ‐BDP‐C tetrad can be used for further derivatization with complex structures. Due extended π‐conjugation presence intramolecular charge transfer band from Fc BDP,...

10.1002/hlca.202300039 article EN Helvetica Chimica Acta 2023-04-21
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