Camil Benbouziyane

ORCID: 0009-0008-1399-416X
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About
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Photopolymerization techniques and applications
  • Photochromic and Fluorescence Chemistry
  • Adenosine and Purinergic Signaling
  • Advanced Polymer Synthesis and Characterization
  • Radical Photochemical Reactions
  • Ionic liquids properties and applications
  • Synthesis and Biological Evaluation
  • Polyoxometalates: Synthesis and Applications
  • CO2 Reduction Techniques and Catalysts
  • Phenothiazines and Benzothiazines Synthesis and Activities

Centre Interdisciplinaire de Nanoscience de Marseille
2023

Centre National de la Recherche Scientifique
2023

Robert Bosch (Germany)
2023

Aix-Marseille Université
2023

A near-infrared-absorbing heptamethine (HM+ ) incorporating three bulky benzo[cd]indole heterocycles was designed to efficiently prevent self-aggregation of the dye, which results in a strong enhancement its photoinitiating reactivity as compared parent bis-benzo[cd]indole (HMCl+ used reference system. In this context, we highlight an efficient free-radical NIR-polymerization up 100 % acrylates C=C bonds conversion even under air conditions. Such important initiating performance obtained by...

10.1002/anie.202305963 article EN Angewandte Chemie International Edition 2023-08-04

The straightforward access to N- or C-substituted dinitro-tetraamino-phenazines (P1–P5) is enabled in oxidative conditions via formation of two intermolecular C–N bonds from accessible 5-nitrobenzene-1,2,4-triamine precursors. photophysical studies revealed green absorbing and orange-red emitting dyes, with enhanced fluorescence the solid state. Further reduction nitro functions led isolation a benzoquinonediimine-fused quinoxaline (P6), which undergoes diprotonation form dicationic coupled...

10.1021/acs.orglett.3c01251 article EN Organic Letters 2023-05-22

Abstract A near‐infrared‐absorbing heptamethine ( HM + ) incorporating three bulky benzo[ cd ]indole heterocycles was designed to efficiently prevent self‐aggregation of the dye, which results in a strong enhancement its photoinitiating reactivity as compared parent bis‐benzo[ HMCl used reference system. In this context, we highlight an efficient free‐radical NIR‐polymerization up 100 % acrylates C=C bonds conversion even under air conditions. Such important initiating performance obtained...

10.1002/ange.202305963 article EN Angewandte Chemie 2023-08-04

…were employed for selective cationic dimerization of a-methylstyrene (aMS) derivatives to synthesize exo-olefin compounds and subsequent sulfur-free RAFT polymerization aMS isobutylene (IB) produce polymers with controlled structures,respectively,a sreported by Masami Kamigaito et al. in their Research Article (e202307791). Nitrogen FixationAn ovel molybdenum complex bearing aP NP-type pincer ligand is reported Kazunari Yoshizawa, Yoshiaki Nishibayashi (e202306631).Thec omplex worked as an...

10.1002/ange.202384311 article EN Angewandte Chemie 2023-10-16
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