Results 1 to 10 of about 38,601 (322)

A visible-light activated secondary phosphine oxide ligand enabling Pd-catalyzed radical cross-couplings [PDF]

open access: yesNature Communications, 2022
Ligand design is key for improving the performance in light-enabled catalytic processes. Here, the authors report the synthesis of a visible-light–activated secondary phosphine oxide ligand and apply it to Pd-catalyzed radical cross-coupling reactions.
Takahito Kuribara   +2 more
doaj   +2 more sources

Phosphine Oxide Indenoquinoline Derivatives: Synthesis and Biological Evaluation as Topoisomerase I Inhibitors and Antiproliferative Agents [PDF]

open access: yesMolecules
The synthesis of phosphorous indenoquinolines and their biological evaluation as topoisomerase 1 (TOP1) inhibitors and antiproliferative agents were performed.
Alba Rodriguez-Paniagua   +4 more
doaj   +2 more sources

Coordination chemistry with phosphine and phosphine oxide-substituted hydroxyferrocenes

open access: yesDalton Transactions, 2010
New unsymmetrical hydroxyferrocenes were synthesised from dibromoferrocene. The oxygen heteroatom was introduced via lithiation and quenching with bis-trimethylsilylperoxide followed by hydrolysis to unmask the hydroxyl functionality. The coordination chemistry of 1'-(diphenylphosphino)-1-hydroxyferrocene 2 was explored with palladium and rhodium ...
Adeleke   +47 more
core   +6 more sources

Bridged [2.2.1] bicyclic phosphine oxide facilitates catalytic γ-umpolung addition-Wittig olefination. [PDF]

open access: yesChem Sci, 2018
A novel bridged [2.2.1] bicyclic phosphine oxide, devised to circumvent the waste generation and burdens of purification that are typical of reactions driven by the generation of phosphine oxides, has been prepared in three steps from commercially ...
Zhang K, Cai L, Yang Z, Houk KN, Kwon O.
europepmc   +3 more sources

Hydrogen-Bonded Di(hydroperoxy)alkane Adducts of the Type Cy3P=O·(HOO)2CHR (R = Alkyl) [PDF]

open access: yesMolecules
Five representatives of a novel type of di(hydroperoxy)alkane adducts of phosphine oxides have been synthesized and fully characterized, including their solubility in organic solvents.
Rahym Ashirov   +3 more
doaj   +2 more sources

Controlled CO labilization of tungsten carbonyl precursors for the low-temperature synthesis of tungsten diselenide nanocrystals

open access: yesFrontiers in Nanotechnology, 2022
We report a low-temperature colloidal synthesis of WSe2 nanocrystals from tungsten hexacarbonyl and diphenyl diselenide in trioctylphosphine oxide (TOPO).
Jessica Q. Geisenhoff   +5 more
doaj   +1 more source

Ortho-Phosphinoarenesulfonamide-Mediated Staudinger Reduction of Aryl and Alkyl Azides

open access: yesMolecules, 2022
Conventional Staudinger reductions of organic azides are sluggish with aryl or bulky aliphatic azides. In addition, Staudinger reduction usually requires a large excess of water to promote the decomposition of the aza-ylide intermediate into phosphine ...
Xingzhuo Li   +5 more
doaj   +1 more source

Phosphineoxide-Chelated Europium(III) Nanoparticles for Ceftriaxone Detection

open access: yesNanomaterials, 2023
The present work demonstrates the optimization of the ligand structure in the series of bis(phosphine oxide) and β-ketophosphine oxide representatives for efficient coordination of Tb3+ and Eu3+ ions with the formation of the complexes exhibiting high ...
Rustem Zairov   +13 more
doaj   +1 more source

Surface Passivation with Selected Phosphine Oxide Molecules for Efficient Pure‐Blue Mixed‐Halide Perovskite Quantum Dot Light‐Emitting Diodes

open access: yesAdvanced Materials Interfaces, 2023
Passivation of defects in halide perovskite using phosphine oxide or alkyl‐phosphonate has recently obtained a few remarkable achievements. However, effective application of phosphine oxide or alky‐phosphonate in passivating perovskite quantum dots (QDs)
Fang Chen   +6 more
doaj   +1 more source

Disulfide Competition for Phosphine Gold(I) Thiolates: Phosphine Oxide Formation vs. Thiolate Disulfide Exchange

open access: yesInorganics, 2015
Phosphine gold(I) thiolate complexes react with aromatic disulfides via two pathways: either thiolate–disulfide exchange or a pathway that leads to formation of phosphine oxide.
Gamage S. P. Garusinghe   +5 more
doaj   +1 more source

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