Results 21 to 30 of about 4,752 (187)
Electron‐beam induced C–F cleavage in –CF3 generates F−, which abstracts a proton to form the acid that catalyzes tBMA deprotection during post‐exposure baking. This self‐sensitization mechanism enables the precise formation of high‐resolution negative‐tone patterns with enhanced sensitivity and resolution.
Yuting Tang +9 more
wiley +1 more source
Synthesis of 1-[1H,1H,2H,2H-perfluooctyl]-3-[2-(oxiran-2-yl)ethyl]imidazolium 4-[(2-oxiran-2-yl)ethoxy]benzenesulfonate as a New Perfluorinated Ionic Monomer [PDF]
Tony Kui +2 more
openalex +1 more source
Ion‐Pairing and Counterion Effects in Contemporary Photochemistry
Ion‐pairing and counterion effects have emerged as fundamental yet underexplored determinants of photochemical behavior. Far from inert, counterions, and Coulombic interactions modulate excited‐state dynamics, quenching efficiencies, emission, and catalytic pathways.
Matthias Schmitz, Christoph Kerzig
wiley +1 more source
5-Formyl-2-methoxyphenyl benzenesulfonate
In the title compound, C14H12O5S, the isovanillin group makes a dihedral angle of 37.45 (15)° with the phenyl ring. The crystal packing is stabilized by a weak non-classical intermolecular C—H⋯O hydrogen bond that links molecules into a chain.
Qiao-Zhen Zhang +3 more
openaire +1 more source
In the environment, bacteria sense aromatic pollutants, migrate toward them, adapt to toxicity, and deploy specialized uptake and catabolic systems. Genomic plasticity, metabolic versatility and division of labor within populations together aid in the degradation of persistent aromatics, highlights that biodegradation is driven by various eco ...
Prashant S. Phale +2 more
wiley +1 more source
A sustainable, ligand‐free Pd‐catalyzed borrowing hydrogen protocol in a biodegradable hydrophobic natural deep eutectic solvent (NADES) (thymol/DL‐menthol) enables the N‐alkylation of primary amines with benzylic alcohols under mild, aerobic conditions, allowing efficient reuse of both catalyst and solvent for seven consecutive cycles. The hydrophobic
Maryam Saeb +5 more
wiley +1 more source
4-Hydroxy-3-nitrophenyl benzenesulfonate
In the title compound, C12H9NO6S, the two aromatic rings form a dihedral angle of 50.0 (2)°. An intermolecular O—H⋯O hydrogen bond is formed between the hydroxy group and the sulfonyl O atom of an adjacent molecule.
Xiujie Ji, Chunbao Li, Chao Liu
openaire +1 more source
Microbial desulfonation of substituted naphthalenesulfonic acids and benzenesulfonic acids [PDF]
Sulfur-limited batch enrichment cultures containing one of nine multisubstituted naphthalenesulfonates and an inoculum from sewage yielded several taxa of bacteria which could quantitatively utilize 19 sulfonated aromatic compounds as the sole sulfur source for growth. Growth yields were about 4 kg of protein per mol of sulfur.
Zürrer, Daniel +2 more
openaire +3 more sources
This review highlights ionic liquid‐based self‐healing polymer electrolytes as a promising route toward safer, resilient solid‐state batteries. By combining nonvolatile plasticization, dynamic supramolecular interactions, and tailored polymer architectures, these materials can simultaneously improve ionic conductivity, mechanical robustness, and ...
Zhijun Wu +6 more
wiley +1 more source
Benzene-1,2,3-triyl tris(benzenesulfonate)
The title compound, C24H18O9S3, crystallizes with two molecules per asymmetric unit, with distinctly different conformations, as quantified by the C—O—S—C torsion angles.
Zhu-Ping Xiao +4 more
openaire +1 more source

