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Reaction of Arylphosphines with Singlet Oxygen: Intra- vs Intermolecular Oxidation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/s0020-1693(00)00190-0openalex-snapshot
M(CO)6 (M=Cr, Mo, W) derivatives of (o-anisyl)diphenylphosphine, bis(o-anisyl)phenylphosphine tris(o-anisyl)phosphine and (p-anisyl)bis(o-anisyl)phosphine
inferredcites →https://doi.org/10.1021/ba-1968-0077.ch068openalex-snapshot
Chemistry of Singlet Oxygen
inferredcites →https://doi.org/10.1021/cr60307a002openalex-snapshot
Steric effects of phosphorus ligands in organometallic chemistry and homogeneous catalysis
inferredcites →https://doi.org/10.1021/ja00064a057openalex-snapshot
Structures and energies of intermediates in the reactions of singlet oxygen with organic phosphines and sulfides
inferredcites →https://doi.org/10.1021/ja00187a071openalex-snapshot
Trimethyl phosphite traps intermediates in the reaction of singlet oxygen (1O2) and diethyl sulfide
inferredcites →https://doi.org/10.1021/ja00352a033openalex-snapshot
Chemistry of singlet oxygen. 45. Mechanism of the photooxidation of sulfides
inferredcites →https://doi.org/10.1021/ja00409a073openalex-snapshot
Chemistry of singlet oxygen. 35. Nature of intermediates in the photooxygenation of sulfides
inferredcites →https://doi.org/10.1021/ja00875a011openalex-snapshot
Autoxidation of Trialkylphosphines
inferredcites →https://doi.org/10.1021/ja973782dopenalex-snapshot
Reaction of Organic Sulfides with Singlet Oxygen. A Revised Mechanism
inferredcites →https://doi.org/10.1063/1.555965openalex-snapshot
Rate Constants for the Decay and Reactions of the Lowest Electronically Excited Singlet State of Molecular Oxygen in Solution. An Expanded and Revised Compilation
inferredcites →https://doi.org/10.5860/choice.38-6192openalex-snapshot
The organometallic chemistry of the transition metals
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ange.201000520openalex-snapshot
Reaction of Singlet Dioxygen with Phosphine–Borane Derivatives: From Transient Phosphine Peroxides to Crystalline Peroxoboronates
inferred← citeshttps://doi.org/10.1002/anie.201000520openalex-snapshot
Reaction of Singlet Dioxygen with Phosphine–Borane Derivatives: From Transient Phosphine Peroxides to Crystalline Peroxoboronates
inferred← citeshttps://doi.org/10.1002/asia.201901275openalex-snapshot
ortho‐Oxygenative 1,2‐Difunctionalization of Diarylalkynes under Merged Gold/Organophotoredox Relay Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201500479openalex-snapshot
Measuring Cumulative Exposure to Oxygen with a Diphenylphosphine–Alkyl Naphthaleneimide Luminescence Turn‐On Dyad
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A General Strategy for Increasing the Air Stability of Phosphines Including Primary Phosphines
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Are Monophospha(III)amidines and ‐guanidines with Ionizable Hydrogens Tautomeric? Towards a Deeper Understanding of Two Related Hetero‐element Functional Groups
inferred← citeshttps://doi.org/10.1002/poc.3383openalex-snapshot
Combination of LFP-TRIR spectroscopy and DFT computation as a tool to determine the intermediate during the photooxidation of triarylphosphine
inferred← citeshttps://doi.org/10.1002/smll.76102openalex-snapshot
Switching Reactivity With Light: C─P Bonding Controls Singlet Oxygen Generation and Reactivity in Dimethyldihydropyrene‐Cyclophanediene (DHP‐CPD) Photoswitches
inferred← citeshttps://doi.org/10.1007/s11172-024-4367-7openalex-snapshot
Triphenylphosphine in the identification of oxidation products of organic compounds with molecular oxygen and peroxides
inferred← citeshttps://doi.org/10.1016/j.carbon.2012.02.033openalex-snapshot
Synthesis, characterization and thermal decomposition behaviour of triphenylphosphine-linked multiwalled carbon nanotubes
inferred← citeshttps://doi.org/10.1016/j.cplett.2008.11.034openalex-snapshot
Photoinduced oxidation of triphenylphosphine isolated in a low-temperature oxygen matrix
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.132538openalex-snapshot
Singlet oxygen: Properties, generation, detection, and environmental applications
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2011.09.001openalex-snapshot
Quantification of thiopurine/UVA-induced singlet oxygen production
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2023.115354openalex-snapshot
Aerobic Self-Photooxidation of Arylphosphines Studied by Steady State and Laser Flash Photolyses
inferred← citeshttps://doi.org/10.1016/j.materresbull.2021.111540openalex-snapshot
Selective Photooxygenation of Dihydroartemisinic Acid in a Reusable Microreactor with Physically Immobilized Photocatalysts
inferred← citeshttps://doi.org/10.1016/j.tet.2005.04.017openalex-snapshot
Advances in singlet oxygen chemistry
inferred← citeshttps://doi.org/10.1016/j.tet.2006.07.112openalex-snapshot
Chemistry of singlet oxygen with arylphosphines
inferred← citeshttps://doi.org/10.1016/j.tet.2006.08.095openalex-snapshot
Possible singlet oxygen generation from the photolysis of indigo dyes in methanol, DMSO, water, and ionic liquid, 1-butyl-3-methylimidazolium tetrafluoroborate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.03.086openalex-snapshot
(Co)oxidation/cyclization processes upon irradiation of triphenylamine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.09.031openalex-snapshot
Visible light-induced 4-phenylthioxanthone-catalyzed aerobic oxidation of triarylphosphines
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02088openalex-snapshot
Reactive Oxygen Species (ROS)-vs Peroxyl-Mediated Photosensitized Oxidation of Triphenylphosphine: A Comparative Study
inferred← citeshttps://doi.org/10.1021/acsomega.9b00831openalex-snapshot
Probing the Formation of Reactive Oxygen Species by a Porous Self-Assembled Benzophenone Bis-Urea Host
inferred← citeshttps://doi.org/10.1021/am9003039openalex-snapshot
pH-Responsive, TiO2-Attached Porphyrin for Singlet Oxygen Production in an Aqueous Solution
inferred← citeshttps://doi.org/10.1021/cr0400717openalex-snapshot
Rather Exotic Types of Cyclic Peroxides: Heteroatom Dioxiranes
inferred← citeshttps://doi.org/10.1021/ef020028ropenalex-snapshot
Model Studies Examining the Use of Dicyclohexylphenylphosphine to Enhance the Oxidative and Thermal Stability of Future Jet Fuels
inferred← citeshttps://doi.org/10.1021/jacs.4c01748openalex-snapshot
Phosphorus-Ligand Redox Cooperative Catalysis: Unraveling Four-Electron Dioxygen Reduction Pathways and Reactive Intermediates
inferred← citeshttps://doi.org/10.1021/jacsau.6c00783openalex-snapshot
Comprehensive Evaluation of Oxidation Resistance for Tertiary Phosphines Using Universal Machine Learning Interatomic Potential-Aided Molecular Dynamics Simulation
inferred← citeshttps://doi.org/10.1021/jp109590topenalex-snapshot
Direct Observation and Quantitative Characterization of Singlet Oxygen in Aqueous Solution upon UVA Excitation of 6-Thioguanines
inferred← citeshttps://doi.org/10.1021/ol0622007openalex-snapshot
Intramolecular Arene Epoxidation by Phosphadioxiranes
inferred← citeshttps://doi.org/10.1021/ol101122uopenalex-snapshot
Photooxidation of Mixed Aryl and Biarylphosphines
inferred← citeshttps://doi.org/10.1021/ol900222vopenalex-snapshot
Preparation of Diphenyl Phosphide and Substituted Phosphines using Alkali Metal in Silica Gel (M−SG)
inferred← citeshttps://doi.org/10.1021/ol900240sopenalex-snapshot
Aerobic Photooxidation of Phosphite Esters Using Diorganotelluride Catalysts
inferred← citeshttps://doi.org/10.1039/9781837676552-00302openalex-snapshot
Singlet oxygen in organic photochemistry
inferred← citeshttps://doi.org/10.1039/b611359aopenalex-snapshot
Oxygen insertion in a carbon–phosphorus bond of the phenylethynyl-di-(tert-butyl)-phosphine bridged dicobalt complex: exploring the nature of oxygen migration using DFT
inferred← citeshttps://doi.org/10.1039/c6ra25469aopenalex-snapshot
Eosin Y-catalyzed photooxidation of triarylphosphines under visible light irradiation and aerobic conditions
inferred← citeshttps://doi.org/10.1039/c8cc08945kopenalex-snapshot
Oxidation of a phosphinidene oxide: formation of a dioxaphosphirane oxide with oxygen scrambling
inferred← citeshttps://doi.org/10.1039/c8cs00830bopenalex-snapshot
The anionic Fries rearrangement: a convenient route to ortho -functionalized aromatics
inferred← citeshttps://doi.org/10.1039/c9dt03367jopenalex-snapshot
Spectroscopic identification of monomeric methyl metaphosphate
inferred← citeshttps://doi.org/10.1039/d1nj03101eopenalex-snapshot
Photochemistry of triphenylamine (TPA) in homogeneous solution and the role of transient N -phenyl-4 a ,4 b -dihydrocarbazole. A steady-state and time-resolved investigation
inferred← citeshttps://doi.org/10.1039/d2cc00782gopenalex-snapshot
Catalytic aerobic photooxidation of triarylphosphines using dibenzo-fused 1,4-azaborines
inferred← citeshttps://doi.org/10.1039/d2cc05336eopenalex-snapshot
Hydrazone-based boron difluoride complexes as triplet photosensitizers for singlet oxygen generation
inferred← citeshttps://doi.org/10.1039/d2qo01005dopenalex-snapshot
Dioxiranes: a half-century journey
inferred← citeshttps://doi.org/10.1055/a-2577-7703openalex-snapshot
Selective Catalytic Aerobic Photooxidation of Thioethers to Sulfoxides
inferred← citeshttps://doi.org/10.1055/sos-sd-131-00192openalex-snapshot
31.41.3 Arylphosphine Oxides and Heteroatom Derivatives (Update 2015)
inferred← citeshttps://doi.org/10.1126/science.1089145openalex-snapshot
Phosphadioxirane: A Peroxide from an Ortho-Substituted Arylphosphine and Singlet Dioxygen
inferred← citeshttps://doi.org/10.1246/cl.130258openalex-snapshot
DFT Computations to Simulate the IR Spectrum of a Transient Intermediate Generated upon Laser Flash Photolysis of Triarylphosphines
inferred← citeshttps://doi.org/10.17533/udea.redin.20200477openalex-snapshot
A kinetic study of the photoinduced oxo-transfer using a Mo complex anchored to TiO2
inferred← citeshttps://doi.org/10.70675/0be9e795z433az4585zb1ffza38c764401a1openalex-snapshot
Etude expérimentale et modélisation d'une réaction de photooxygénation avec sensibilisateur soluble ou supporté dans des photoréacteurs continus milli-structurés éclairés par des LED
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