Results 261 to 270 of about 1,029,734 (328)

Investigating the Structure–Function Relationships of Fluorinated Interfaces for PFAS Capture and Electrochemically‐Mediated Release

open access: yesAdvanced Functional Materials, EarlyView.
This study explores the use of fluorinated copolymers with varying fluorophilic side chain lengths to enhance PFAS affinity. The integration of electrochemical techniques demonstrates enhanced adsorbent regeneration, with molecular dynamics simulations providing insight into the molecular‐level interactions involved.
Anaira Román Santiago   +7 more
wiley   +1 more source

Vanadium Doped Magnetic MoS2 Monolayers of Improved Electrical Conductivity as Spin‐Orbit Torque Layer

open access: yesAdvanced Functional Materials, EarlyView.
Electrically conductive and room temperature magnetic atomically thin (≈0.8 nm) vanadium doped MoS2 (V‐MoS2) is demonstrated for its spintronic applications. Here, the spin transport at the interface of permalloy (Py) and high spin‐orbit coupling V‐MoS2 magnetic monolayers is shown.
Krishna Rani Sahoo   +8 more
wiley   +1 more source

Coupling Interfacial Redox‐Reactions with In Situ Proton Generation for the Photoelectrochemical Separation of Rare‐Earth Elements

open access: yesAdvanced Functional Materials, EarlyView.
To enhance the sustainability of electrochemical separations for resource recovery, a photoelectrochemical ion recovery system is developed that utilizes renewable solar energy. A composite integrating titianium dioxide nanorods and a redox‐copolymer enables spontaneous cation adsorption and light‐activated redox reactions for regeneration, thus ...
Ki‐Hyun Cho   +3 more
wiley   +1 more source

Ultrafast Energy Transfer Induced Lasing From a Coplanar Donor‐Acceptor‐Donor Molecule in a Microspherical Cavity

open access: yesAdvanced Functional Materials, EarlyView.
This study presents a novel donor‐bridge‐acceptor‐bridge‐donor (D‐B‐A‐B‐D) molecular system, which shows near‐unity intramolecular excitation energy transfer (IET) from two identical energy donors to a coplanar acceptor. It enables a four‐level energy system for efficient lasing at the acceptor emission band in a microspherical cavity with a low lasing
Vishal Kumar   +6 more
wiley   +1 more source

Fmoc Solid-Phase Peptide Synthesis.

Methods in molecular biology, 2015
Synthetic peptides are important as drugs and in research. Currently, the method of choice for producing these compounds is solid-phase peptide synthesis. In this nonspecialist review, we describe the scope and limitations of Fmoc solid-phase peptide synthesis. Furthermore, we provide a detailed protocol for Fmoc peptide synthesis.
P. Hansen, Alberto Oddo
semanticscholar   +6 more sources

Solid phase synthesis of praziquantel [PDF]

open access: possibleTetrahedron Letters, 2006
The first solid phase synthesis of the important anthelmintic praziquantel is described. The synthesis is rapid and efficient. The method may be extended to the synthesis of libraries of urgently needed replacements for this drug.
Shaimaa El-Fayyoumy   +3 more
openaire   +2 more sources

Solid phase synthesis of oligosaccharides

Tetrahedron Letters, 1996
Abstract An efficient and stereocontrolled solid-phase chemical synthesis of oligosaccarides using a new type of insoluble support (a copolymer of polyethylene glycol and polystyrene) is described. Several Lewis acids were tested as activators of the trichloroacetimidate 12 , used as glycosyl donor, in the dimer 13 formation.
ADINOLFI M   +4 more
openaire   +4 more sources

Enantioselective Synthesis on the Solid Phase

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Herbert Waldmann, Torben Leßmann
openaire   +3 more sources

Solid phase synthesis of benzimidazolones

Tetrahedron Letters, 1996
Abstract An efficient solid phase synthesis of benzimidazoles is described. Polymer bound o-fluoronitroaromatic compound 2 was treated with an amine to give o-nitroaniline derivative 3 . Reduction of 3 with NaBH 4 Cu(acac) 2 followed by cyclization with an aryl imidate and cleavage with TFA gave 5 .
Gary B. Phillips, Guo Ping Wei
openaire   +3 more sources

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