Sidonie Laviéville

ORCID: 0009-0003-7178-245X
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About
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Carbon dioxide utilization in catalysis
  • Polymer composites and self-healing
  • Oxidative Organic Chemistry Reactions
  • Synthetic Organic Chemistry Methods
  • Fluorine in Organic Chemistry
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • biodegradable polymer synthesis and properties
  • Catalysis for Biomass Conversion
  • Asymmetric Synthesis and Catalysis
  • Covalent Organic Framework Applications
  • Advanced Polymer Synthesis and Characterization

Université de Montpellier
2023-2025

Centre National de la Recherche Scientifique
2022-2025

École Nationale Supérieure de Chimie de Montpellier
2023-2025

Institut de Recherche de Chimie Paris
2022

Chimie ParisTech
2022

Université Paris Sciences et Lettres
2022

The present perspective provides an overview of the hemiacetal ester (HAE) chemical functionality and its use in organic synthesis polymer science. objective is to expose high potential HAE both molecular macromolecular chemistry through highlighting rich peculiar reactivity describing achievements involving this group. We a summary different synthetic routes described so far produce HAEs, whether led linear or cyclic compounds. also outline very complex functional group thorough description...

10.1021/acs.macromol.3c01250 article EN Macromolecules 2024-01-20

Robust homoleptic zinc catalysts offer new opportunities for recycling polyesters such as poly(lactic acid) and poly(ethylene terephthalate) to obtain platform molecules in a plastics circular economy approach.

10.1039/d2cy01092e article EN cc-by-nc Catalysis Science & Technology 2022-01-01

This work presents the synthesis and characterization of a highly transparent colorless covalent adaptable network (CAN) exhibiting short relaxation times (30 s at 150 °C) limited creep 100 °C. Based on N,S-acetal functions, strongly stabilized by trifluoromethyl group, this network, however, retains ability to undergo fast thiol exchanges. The present article describes detailed monitoring cross-linking via ATR-FTIR 19F HRMAS NMR (high-resolution magic angle spinning NMR), complete...

10.1021/acs.macromol.4c01359 article EN Macromolecules 2024-10-19

Abstract The enantioselective addition of difluoroenoxysilanes to aromatic aldehydes, catalyzed by cationic palladium aqua complexes, has been described. reaction is operationally simple, does not require anhydrous conditions and performs at room temperature. catalysts, previously discovered reported Sodeoka, are easily prepared in two steps from PdCl 2 (MeCN) . aldol compounds were obtained good yields with enantiomeric ratios up 93 : 7, the being more efficient using electron‐rich aldehydes.

10.1002/ejoc.202300467 article EN cc-by-nc European Journal of Organic Chemistry 2023-06-29
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