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Kinetic applications of electron paramagnetic resonance spectroscopy. XXII. Dialkylaminothiyl radicals

https://doi.org/10.1021/ja00418a032
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inferred← citeshttps://doi.org/10.2139/ssrn.4650814openalex-extracted
inferred← citeshttps://doi.org/10.1002/9780470034408.ch8openalex-snapshot
Thiyl radicals
inferred← citeshttps://doi.org/10.1002/9780470772195.ch4openalex-snapshot
Nitroxides
inferred← citeshttps://doi.org/10.1002/9780470772287.ch4openalex-snapshot
NMR and ESR of sulphenic acids and their derivatives
inferred← citeshttps://doi.org/10.1002/ange.201611049openalex-snapshot
Thermally Adjustable Dynamic Disulfide Linkages Mediated by Highly Air‐Stable 2,2,6,6‐Tetramethylpiperidine‐1‐sulfanyl (TEMPS) Radicals
inferred← citeshttps://doi.org/10.1002/anie.201611049openalex-snapshot
Thermally Adjustable Dynamic Disulfide Linkages Mediated by Highly Air‐Stable 2,2,6,6‐Tetramethylpiperidine‐1‐sulfanyl (TEMPS) Radicals
inferred← citeshttps://doi.org/10.1002/chem.201504900openalex-snapshot
Synthesis and Rearrangement of P‐Nitroxyl‐Substituted PIII and PV Phosphanes: A Combined Experimental and Theoretical Case Study
inferred← citeshttps://doi.org/10.1002/chem.201800118openalex-snapshot
Sulfones as Synthetic Linchpins: Transition‐Metal‐Free sp3–sp2 and sp2–sp2 Cross‐Couplings Between Geminal Bis(sulfones) and Organolithium Compounds
inferred← citeshttps://doi.org/10.1002/chin.197615126openalex-snapshot
ChemInform Abstract: KINETIC APPLICATIONS OF ELECTRON PARAMAGNETIC RESONANCE SPECTROSCOPY. XXII. DIALKYLAMINOTHIYL RADICALS
inferred← citeshttps://doi.org/10.1002/hlca.202500106openalex-snapshot
TEMPS, the Chalcogen Cousin of the Infamous Stable Radical TEMPO, Traps Radicals via Substitution on Its Dimer (TEMPS)2
inferred← citeshttps://doi.org/10.1002/marc.202100118openalex-snapshot
Acyclic Diene Metathesis (ADMET) Polymerization of 2,2,6,6‐Tetramethylpiperidine‐1‐sulfanyl (TEMPS) Dimers
inferred← citeshttps://doi.org/10.1002/marc.202400303openalex-snapshot
Reprocessable Polymer Networks Containing Sulfur‐Based, Percolated Dynamic Covalent Cross‐Links and Percolated or Non‐Percolated, Static Cross‐Links
inferred← citeshttps://doi.org/10.1002/mrc.1260280302openalex-snapshot
Electron spin resonance spectroscopy of free radicals containing sulphur linked to nitrogen
inferred← citeshttps://doi.org/10.1002/zfch.19870270104openalex-snapshot
Thiolierungsreagenzien in der organischen Chemie
inferred← citeshttps://doi.org/10.1007/10201276_168openalex-snapshot
6.44 Ferro-, manganeso-, rhenio-, molybdeno-nitroxides
inferred← citeshttps://doi.org/10.1007/10201276_169openalex-snapshot
6.45 Thio nitroxides
inferred← citeshttps://doi.org/10.1007/10201276_170openalex-snapshot
60Ulb1 - 72Mot1
inferred← citeshttps://doi.org/10.1007/10201284_36openalex-snapshot
10.1.1.1 Thiyl radicals
inferred← citeshttps://doi.org/10.1007/10201284_44openalex-snapshot
10.3 References for 10.1 and 10.2
inferred← citeshttps://doi.org/10.1007/10201373_57openalex-snapshot
6.2 Iminoxyl radicals, RR’C=NO
inferred← citeshttps://doi.org/10.1007/10201373_58openalex-snapshot
6.3 Aminothiyl radicals, RRNS, iminothiyl radicals, RR’C=NS, and related species
inferred← citeshttps://doi.org/10.1007/10201373_59openalex-snapshot
References for 6.1 - 6.3
inferred← citeshttps://doi.org/10.1007/10201373_64openalex-snapshot
7.4 Sulfur-centered radicals
inferred← citeshttps://doi.org/10.1007/10201373_69openalex-snapshot
References for 7.1 - 7.8
inferred← citeshttps://doi.org/10.1007/10348248_125openalex-snapshot
5.13 (Azo)oxyl radicals
inferred← citeshttps://doi.org/10.1007/10348248_126openalex-snapshot
5.14 Iminothiyl radicals
inferred← citeshttps://doi.org/10.1007/10348248_127openalex-snapshot
5.15 References for 5
inferred← citeshttps://doi.org/10.1007/978-981-16-6807-4_27openalex-snapshot
Transforming Cyclic/Linear Polymer Topologies: Emerging Techniques and Opportunities
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00117-0openalex-snapshot
Chalcogen–Nitrogen Radicals
inferred← citeshttps://doi.org/10.1016/b978-0-12-040705-7.50013-8openalex-snapshot
CHALCOGENS
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2023.112661openalex-snapshot
Covalent adaptable networks and thermosets of multi-block ethylene/1-octene copolymers made by free-radical processing: Effects of melt flow index and crystallinity on thermomechanical properties and reprocessability
inferred← citeshttps://doi.org/10.1016/j.ijadhadh.2019.03.011openalex-snapshot
Covalent cross-linking of polymers at room temperature
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)86400-0openalex-snapshot
Stereochemical course of the [2,3]-sigmatropic rearrangement of substituted propargyl n,n-dialkylamidosulfoxylates. X-ray molecular structure of [S*, (S)R*]-4-[(1,4,4-trimethyl-1,2-pentadienyl)sulfinyl]-morpholine.
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)83254-8openalex-snapshot
Synthesis of thiophenes from acetylenes and -amine disulfides
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)95123-8openalex-snapshot
1,2-thiazet-2-yle, eine neue klasse stabiler radikale
inferred← citeshttps://doi.org/10.1021/acs.chemmater.1c03678openalex-snapshot
Stimuli-Responsive Covalent Adaptable Hydrogels Based on Homolytic Bond Dissociation and Chain Transfer Reactions
inferred← citeshttps://doi.org/10.1021/acs.jpca.5b12674openalex-snapshot
The Dimerization of H2NO
inferred← citeshttps://doi.org/10.1021/acs.macromol.0c00798openalex-snapshot
Rational Entry to Cyclic Polymers via Thermally Induced Radical Ring-Expansion Polymerization of Macrocycles with One Bis(hindered amino)disulfide Linkage
inferred← citeshttps://doi.org/10.1021/acs.macromol.0c01539openalex-snapshot
Recyclable Polymethacrylate Networks Containing Dynamic Dialkylamino Disulfide Linkages and Exhibiting Full Property Recovery
inferred← citeshttps://doi.org/10.1021/acs.macromol.3c02515openalex-snapshot
Covalent Adaptable Networks Made by Reactive Processing of Highly Entangled Polymer: Synthesis-Structure-Thermomechanical Property-Reprocessing Relationship in Covalent Adaptable Networks
inferred← citeshttps://doi.org/10.1021/acs.macromol.5c01213openalex-snapshot
Recyclable Ethylene-Vinyl Acetate Covalent Adaptable Networks and Their Structure–Property Relationships
inferred← citeshttps://doi.org/10.1021/acsapm.4c01580openalex-snapshot
Reprocessable Covalent Adaptable Networks via Free-Radical Polymerization with an Aromatic Disulfide Cross-Linker
inferred← citeshttps://doi.org/10.1021/acsmacrolett.7b00762openalex-snapshot
Thermally Healable and Reprocessable Bis(hindered amino)disulfide-Cross-Linked Polymethacrylate Networks
inferred← citeshttps://doi.org/10.1021/ic9614879openalex-snapshot
Products and Mechanisms in the Oxidation of Phosphorus by Sulfur at Low Temperature
inferred← citeshttps://doi.org/10.1021/ma902596sopenalex-snapshot
Covalent Adaptable Networks (CANs): A Unique Paradigm in Cross-Linked Polymers
inferred← citeshttps://doi.org/10.1039/b617142gopenalex-snapshot
What's new in stable radical chemistry?
inferred← citeshttps://doi.org/10.1039/c39930001684openalex-snapshot
The synthesis and X-ray structural characterisation of an unusual seven-membered diaza-phospha-tetrathia heterocycle
inferred← citeshttps://doi.org/10.1039/c9qm00488bopenalex-snapshot
Dynamic covalent bonds: approaches from stable radical species
inferred← citeshttps://doi.org/10.1039/d1py00187fopenalex-snapshot
Reprocessable covalent adaptable networks with excellent elevated-temperature creep resistance: facilitation by dynamic, dissociative bis(hindered amino) disulfide bonds
inferred← citeshttps://doi.org/10.1039/d2ta06364fopenalex-snapshot
Simple upcycling of virgin and waste polyethylene into covalent adaptable networks: catalyst-free, radical-based reactive processing with dialkylamino disulfide bonds
inferred← citeshttps://doi.org/10.1039/d3py00444aopenalex-snapshot
Novel covalent adaptable networks (CANs) of ethylene/1-octene copolymers (EOCs) made by free-radical processing: comparison of structure–property relationships of EOC CANs with EOC thermosets
inferred← citeshttps://doi.org/10.1039/d3py00498hopenalex-snapshot
Reprocessable, creep-resistant covalent adaptable networks synthesized using conventional free-radical polymerization conditions with piperidine-based and non-piperidine-based dynamic dialkylamino disulfide chemistry
inferred← citeshttps://doi.org/10.1039/d3tc00117bopenalex-snapshot
Carbon-centered radical based dynamic covalent chemistry for stimuli-responsive chromic materials
inferred← citeshttps://doi.org/10.11618/adhesion.55.168openalex-snapshot
Reactive Polyurethanes with Dynamic Covalent Linkages
inferred← citeshttps://doi.org/10.70675/725f3644z06ecz47e6z9db2z9a39f6ed36a7openalex-snapshot
Développement de méthodes analytiques pour la caractérisaton de lots industriels du nitroxyde SG1
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