Relevant bibliographies by topics / Sels de diaryliodonium

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Sels de diaryliodonium'

Author: Grafiati
Published: 30 November 2024
Last updated: 31 July 2025

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Journal articles on the topic "Sels de diaryliodonium"

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Battioni, Jean-Paul, Daniel Dupré, Marcel Delaforge, Maryse Jaouen та Daniel Mansuy. "Réactions des dérivés de l'iode(III) avec les ferroporphyrines et le cytochrome P-450: Formation de complexes σ-aryles du fer(III) et de N-aryl-porphyrines du fer(II) à partir de sels de diaryliodonium". Journal of Organometallic Chemistry 358, № 1-3 (1988): 389–400. http://dx.doi.org/10.1016/0022-328x(88)87092-x.

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2

Suslonov, Vitalii V., Natalia S. Soldatova, Pavel S. Postnikov, et al. "Diaryliodonium Tetracyanidometallates Self-Assemble into Halogen-Bonded Square-Like Arrays." Crystal Growth & Design 22, no. 4 (2022): 2749–58. http://dx.doi.org/10.1021/acs.cgd.2c00175.

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Radzhabov, Amirbek D., Alyona I. Ledneva, Natalia S. Soldatova, et al. "Halogen Bond-Involving Self-Assembly of Iodonium Carboxylates: Adding a Dimension to Supramolecular Architecture." International Journal of Molecular Sciences 24, no. 19 (2023): 14642. http://dx.doi.org/10.3390/ijms241914642.

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We designed 0D, 1D, and 2D supramolecular assemblies made of diaryliodonium salts (functioning as double σ-hole donors) and carboxylates (as σ-hole acceptors). The association was based on two charge-supported halogen bonds (XB), which occurred between IIII sites of the iodonium cations and the carboxylate anions. The sequential introduction of the carboxylic groups in the aryl ring of the benzoic acid added a dimension to the 0D supramolecular organization of the benzoate, which furnished 1D-chained and 2D-layered structures when terephthalate and trimesate anions, correspondingly, were appli
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4

Malik, Muhammad Salman, Sandra Schlögl, Markus Wolfahrt, and Marco Sangermano. "Review on UV-Induced Cationic Frontal Polymerization of Epoxy Monomers." Polymers 12, no. 9 (2020): 2146. http://dx.doi.org/10.3390/polym12092146.

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Ultraviolet (UV)-induced cationic frontal polymerization has emerged as a novel technique that allows rapid curing of various epoxy monomers upon UV irradiation within a few seconds. In the presence of a diaryliodonium salt photoinitiator together with a thermal radical initiator, the cationic ring opening polymerization of an epoxide monomer is auto-accelerated in the form of a self-propagating front upon UV irradiation. This hot propagating front generates the required enthalpy to sustain curing reaction throughout the resin formulation without further need for UV irradiation. This unique re
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Zhang, Jie, Aiyou Hao, and Pengyao Xing. "Hypervalent Iodine(III) Mediated Halogen Bonded Supramolecular Chiral System with Cholesteryl Naphthalimides." Chemistry – A European Journal, April 7, 2024. http://dx.doi.org/10.1002/chem.202401004.

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Halogen bonding acknowledged as a noteworthy weak interaction, has gained growing recognition in the field of supramolecular chemistry. In this study, we selected structurally rigid diaryliodonium ions (I(III)) with two biaxial σ‐holes as halogen‐bond donors, to bind with three chiral acceptor molecules bearing cholesteryl and naphthalimides with distinct geometries. The abundant carbonyl oxygen atoms in side‐arm substituents function as multiple acceptors for halogen bonding. The self‐aggregation of chiral acceptor molecules demonstrates adaptiveness to solvent media, evidenced by the inversi
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Dissertations / Theses on the topic "Sels de diaryliodonium"

1

Marchal, Lucas. "Synthèse de nouveaux candidats médicamenteux présentant une chiralité axiale C-N par le développement de nouveaux couplages C-N atroposélectifs." Electronic Thesis or Diss., Strasbourg, 2024. http://www.theses.fr/2024STRAF029.

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Les composés à chiralité axiale C–N ont démontré un potentiel significatif dans divers domaines, en particulier dans l'industrie pharmaceutique. Cependant, il existe actuellement peu de méthodologies connues permettant d’accéder à ces composés, et elles sont généralement limitées à des structures moléculaires très spécifiques. Afin de préparer de nouveaux atropisomères C–N d'intérêt, des méthodologies synthétiques innovantes doivent être développées. À cette fin, nous avons concentré nos efforts sur l'utilisation de sels de diaryliodonium comme partenaires de couplage hautement réactifs, ce qu
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