Results 31 to 40 of about 4,140 (141)

Microbial desulfonation of substituted naphthalenesulfonic acids and benzenesulfonic acids [PDF]

open access: yesApplied and Environmental Microbiology, 1987
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

Delicate design of lithium‐ion bridges in hybrid solid electrolyte for wide‐temperature adaptive solid‐state lithium metal batteries

open access: yesInfoMat, Volume 8, Issue 3, March 2026.
A well‐designed hybrid solid electrolyte with stable lithium‐ion bridges via chemical linkages across the ceramic electrolyte phase and the polymer chain has been developed. This easily scale‐up hybrid solid‐state electrolyte with superior electrochemical properties withstands extreme operational challenges, that is, high‐rate cycling (4 C) and wide ...
Yuchen Wang   +8 more
wiley   +1 more source

Wireless Electromechanical Fluorophore Release From Soft Polymer Actuators

open access: yesMacromolecular Materials and Engineering, Volume 311, Issue 3, March 2026.
Simultaneous wireless electromechanical deformation and fluorescence emission of a polypyrrole‐based composite incorporating a π‐conjugated fluorophore (2’,7’‐bis([2,2’‐bithiophen]‐5‐yl)fluorene) allows mapping of electroactivity via a dual dynamic/light‐emitting readout.
Anaga Vinod   +5 more
wiley   +1 more source

Strategies to Improve the Lipophilicity of Hydrophilic Macromolecular Drugs

open access: yesAdvanced Healthcare Materials, Volume 15, Issue 5, 2 February 2026.
Hydrophilic macromolecular drugs can be successfully lipidized by covalent attachment of lipids, by hydrophobic ion pairing with negatively or positively charged surfactants, and by dry or wet reverse micelle formation. Lipophilicity enhancement of hydrophilic macromolecules has several benefits including stability and bioavailability improvement ...
Sera Lindner   +8 more
wiley   +1 more source

A Reactive Antagonist Strategy: Cysteine‐Directed Covalent Molecular Glue in Plant Hormone Receptor Regulation

open access: yesAdvanced Science, Volume 13, Issue 10, 18 February 2026.
The plant hormone jasmonate is perceived by COI1‐JAZ co‐receptors comprising a single F‐box protein COI1 and multiple JAZ repressors with overlapping functions, complicating genetic analysis. We present a reactive antagonist (RA) strategy that selectively promotes COI1 binding to a cysteine‐engineered JAZ variant while blocking wild‐type JAZs, enabling
Minoru Ueda   +10 more
wiley   +1 more source

Recent Advances in Bioconjugation of Aromatic Amino Acid Residues by a Reactivity‐Guided Approach

open access: yesThe Chemical Record, Volume 26, Issue 2, February 2026.
This review highlights recent advances in the bioconjugation of aromatic amino acids residues, focusing on strategies that leverage their inherent chemical reactivity to enable precise and versatile modifications of biomacromolecules, illustrating relevant applications.
Bruno M. da S. Santos   +3 more
wiley   +1 more source

Sulfur-33 NMR of Benzenesulfonic Acid

open access: yesJournal of Japan Oil Chemists' Society, 1989
For the general use of sulfur-33 NMR spectroscopy, measuring conditions for benzenesulfonic acid were examined. A 0.75M solution (deuterium oxide-water mixture in the ratio of 2: 1) adjusted to pH 6.5-10.5 gave a good signal with line width at half the peak height of 13.5Hz after 3h of data accumulation.
openaire   +2 more sources

3-Hydroxy-4-nitrophenyl benzenesulfonate

open access: yesActa Crystallographica Section E Structure Reports Online, 2006
The asymmetric unit of the title compound, C12H9NO6S, contains two independent mol­ecules. There are significant differences between the torsion angles and dihedral angles of the two mol­ecules. An intra­molecular O—H⋯O hydrogen bond is formed between the hydr­oxy group and the nitro O atom in both mol­ecules.
openaire   +1 more source

Microbial Utilization of Benzenesulfonic Acid

open access: yesAgricultural and Biological Chemistry, 1972
OKI, Toshikazu   +3 more
openaire   +1 more source

Home - About - Disclaimer - Privacy