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Conductive Phosphine Oxide Passivator Enables Efficient Perovskite Light-Emitting Diodes.
Nano letters (Print), 2022Recently, surface passivation has been proved to be an essential approach for obtaining efficient and stable perovskite light-emitting diodes (Pero-LEDs). Phosphine oxides performed well as passivators in many reports.
Mingliang Li+10 more
semanticscholar +1 more source
Journal of the American Chemical Society, 2021
The first highly enantioselective catalytic synthesis of P-stereogenic secondary phosphine-boranes was realized by the asymmetric addition of primary phosphine to electron-deficient alkenes with a newly developed unsymmetric bisphosphine (PCP') pincer ...
Chuanyong Wang+3 more
semanticscholar +1 more source
The first highly enantioselective catalytic synthesis of P-stereogenic secondary phosphine-boranes was realized by the asymmetric addition of primary phosphine to electron-deficient alkenes with a newly developed unsymmetric bisphosphine (PCP') pincer ...
Chuanyong Wang+3 more
semanticscholar +1 more source
Angewandte Chemie, 2021
The catalytic asymmetric synthesis of P-chiral phosphorus compounds is an important way to construct P-chiral ligands. Herein, we report a new strategy that adopts the pyridinyl moiety as the coordination group in the cobalt-catalysed asymmetric ...
Wei-Liang Duan+9 more
semanticscholar +1 more source
The catalytic asymmetric synthesis of P-chiral phosphorus compounds is an important way to construct P-chiral ligands. Herein, we report a new strategy that adopts the pyridinyl moiety as the coordination group in the cobalt-catalysed asymmetric ...
Wei-Liang Duan+9 more
semanticscholar +1 more source
Annual Review of Entomology, 2020
Development of resistance in major grain insect pest species to the key fumigant phosphine (hydrogen phosphide) across the globe has put the viability and sustainability of phosphine in jeopardy.
M. Nayak+3 more
semanticscholar +1 more source
Development of resistance in major grain insect pest species to the key fumigant phosphine (hydrogen phosphide) across the globe has put the viability and sustainability of phosphine in jeopardy.
M. Nayak+3 more
semanticscholar +1 more source
Phosphine-Catalyzed Asymmetric Organic Reactions.
Chemical Reviews, 2018Asymmetric phosphine catalysis showcasing remarkable progress over the past two decades has emerged as a key synthetic platform for the creation of molecular frameworks encountered in medicinal chemistry and materials science.
Huanzhen Ni, Wai-Lun Chan, Yixin Lu
semanticscholar +1 more source
Journal of Medicinal Chemistry, 2020
Phosphine oxides and related phosphorus-containing functional groups such as phosphonates and phosphinates are established structural motifs that are, still, underrepresented in today's drug discovery projects, and only few examples can be found amongst ...
Peter Finkbeiner+2 more
semanticscholar +1 more source
Phosphine oxides and related phosphorus-containing functional groups such as phosphonates and phosphinates are established structural motifs that are, still, underrepresented in today's drug discovery projects, and only few examples can be found amongst ...
Peter Finkbeiner+2 more
semanticscholar +1 more source
Small, 2020
In this work, a phosphine-based covalent organic framework (Phos-COF-1) is successfully synthesized and employed as a template for the confined growth of broad-scope nanoparticles (NPs).
Rao Tao+11 more
semanticscholar +1 more source
In this work, a phosphine-based covalent organic framework (Phos-COF-1) is successfully synthesized and employed as a template for the confined growth of broad-scope nanoparticles (NPs).
Rao Tao+11 more
semanticscholar +1 more source
Organoplumbyl Phosphines and Phosphine Oxides
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
P. J. McCormack, Patrick J. Guiry
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Reduction of phosphine oxides to phosphines
Tetrahedron Letters, 2019Abstract The digest is devoted to the most widespread reducing agents which are used for the reduction of tertiary and secondary phosphine oxides, phospholene oxides, phospholane oxides, phosphonates, phosphinates, α- and β-hydroxy and thiomethyl phosphine oxides, α-aminophosphine oxides. Stereoselectivity of reactions is described.
Ekaterina A. Kuchuk+3 more
openaire +2 more sources
ChemInform, 2009
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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Armin Boerner, Benjamin Schaeffner
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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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Armin Boerner, Benjamin Schaeffner
openaire +2 more sources