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Radical ring‐opening polymerization of lipoates: Kinetic and thermodynamic aspects

https://doi.org/10.1002/pol.20200765

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Radical ring-opening polymerization

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Biochemistry and Chemistry of Lipoic Acids

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Handbook of Ring‐Opening Polymerization

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Synthesis and Peptide‐Induced Degradation of Biocompatible Fibers Based on Highly Branched Poly(2‐hydroxyethyl methacrylate)

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Oxidation of dithiols to polydisulfides by means of dimethylsulfoxide

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Thermal and photoinitiated copolymerization of the cyclic disulfide lipoamide with styrene

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Use of polymerizable ring compounds in constant volume polymerizations

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Studies on the copolymerization of cyclic disulfide lipoamide with styrene. II. Laser flash photolysis investigation

inferredcites →https://doi.org/10.1002/pola.24325openalex-snapshot

Ring‐opening polymerization of lipoic acid and characterization of the polymer

inferredcites →https://doi.org/10.1002/polc.5070120107openalex-snapshot

Polymeric sulfur and related polymers

inferredcites →https://doi.org/10.1002/smll.200900906openalex-snapshot

Stabilization of Polymer‐Hydrogel Capsules via Thiol–Disulfide Exchange

inferredcites →https://doi.org/10.1016/0076-6879(87)43048-6openalex-snapshot

Chemical reduction of disulfides

inferredcites →https://doi.org/10.1016/0891-5849(95)00017-ropenalex-snapshot

Alpha-lipoic acid as a biological antioxidant

inferredcites →https://doi.org/10.1016/b978-0-444-53349-4.00115-1openalex-snapshot

Ring–Chain Equilibria in Ring-Opening Polymerization

inferredcites →https://doi.org/10.1016/j.bbagen.2009.07.026openalex-snapshot

Alpha-lipoic acid as a dietary supplement: Molecular mechanisms and therapeutic potential

inferredcites →https://doi.org/10.1016/j.eurpolymj.2013.03.001openalex-snapshot

Reversible disulphide formation in polymer networks: A versatile functional group from synthesis to applications

inferredcites →https://doi.org/10.1016/s0083-6729(08)60714-1openalex-snapshot

Biochemistry of Lipoic Acid

inferredcites →https://doi.org/10.1016/s0169-409x(02)00179-5openalex-snapshot

Drug delivery strategy utilizing conjugation via reversible disulfide linkages: role and site of cellular reducing activities

inferredcites →https://doi.org/10.1016/s0891-5849(01)00480-4openalex-snapshot

Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple

inferredcites →https://doi.org/10.1021/ac60220a049openalex-snapshot

Reduction of Disulfides with Tributylphosphine.

inferredcites →https://doi.org/10.1021/ja00173a017openalex-snapshot

Predicting the stability of cyclic disulfides by molecular modeling: effective concentrations in thiol-disulfide interchange and the design of strongly reducing dithiols

inferredcites →https://doi.org/10.1021/ja00173a018openalex-snapshot

Degenerate intermolecular thiolate-disulfide interchange involving cyclic five-membered disulfides is faster by .apprx.103 than that involving six- or seven-membered disulfides

inferredcites →https://doi.org/10.1021/ja01103a528openalex-snapshot

Copolymerization of Vinyl Acetate with a Cyclic Disulfide

inferredcites →https://doi.org/10.1021/ja01187a524openalex-snapshot

THE PREPARATION AND POLYMERIZATION OF MONOMERIC CYCLIC DISULFIDES

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The Infra-red Spectra of Complex Molecules.

inferredcites →https://doi.org/10.1021/ja01561a014openalex-snapshot

Kinetics of the Thiol-Disulfide Exchange

inferredcites →https://doi.org/10.1021/ja01600a069openalex-snapshot

Properties and Derivatives of α-Lipoic Acid

inferredcites →https://doi.org/10.1021/ja01604a053openalex-snapshot

Disulfide Polymers of DL-α-Lipoic Acid

inferredcites →https://doi.org/10.1021/ja01607a057openalex-snapshot

Syntheses of DL-α-Lipoic Acid

inferredcites →https://doi.org/10.1021/ja01646a029openalex-snapshot

The Chemistry of 1,2-Dithiolane (Trimethylene Disulfide) as a Model for the Primary Quantum Conversion Act in Photosynthesis1a

inferredcites →https://doi.org/10.1021/ja311961kopenalex-snapshot

Substrate-Initiated Synthesis of Cell-Penetrating Poly(disulfide)s

inferredcites →https://doi.org/10.1021/ja501581bopenalex-snapshot

Cellular Uptake of Substrate-Initiated Cell-Penetrating Poly(disulfide)s

inferredcites →https://doi.org/10.1021/jacs.7b00039openalex-snapshot

1,2-Dithiolane-Derived Dynamic, Covalent Materials: Cooperative Self-Assembly and Reversible Cross-Linking

inferredcites →https://doi.org/10.1021/jacs.9b08957openalex-snapshot

Architecture-Controlled Ring-Opening Polymerization for Dynamic Covalent Poly(disulfide)s

inferredcites →https://doi.org/10.1021/jo01150a024openalex-snapshot

THE PREPARATION AND RELATIVE REACTIVITIES OF MANY-MEMBERED CYCLIC DISULFIDES

inferredcites →https://doi.org/10.1021/ma00208a004openalex-snapshot

Radical copolymerization of lipoamide with vinyl monomers

inferredcites →https://doi.org/10.1021/ma021061fopenalex-snapshot

Reversible Redox Cleavage/Coupling of Polystyrene with Disulfide or Thiol Groups Prepared by Atom Transfer Radical Polymerization

inferredcites →https://doi.org/10.1021/ma050020ropenalex-snapshot

Combining Atom Transfer Radical Polymerization and Disulfide/Thiol Redox Chemistry: A Route to Well-Defined (Bio)degradable Polymeric Materials

inferredcites →https://doi.org/10.1021/ma060063nopenalex-snapshot

Copolymerization of Lipoic Acid with 1,2-Dithiane and Characterization of the Copolymer as an Interlocked Cyclic Polymer

inferredcites →https://doi.org/10.1021/ma0604035openalex-snapshot

Synthesis of Reversible Shell Cross-Linked Micelles for Controlled Release of Bioactive Agents

inferredcites →https://doi.org/10.1021/ma991264copenalex-snapshot

Using Atom Transfer Radical Polymerization To Amplify Monolayers of Initiators Patterned by Microcontact Printing into Polymer Brushes for Pattern Transfer

inferredcites →https://doi.org/10.1038/npg.els.0000631openalex-snapshot

Coenzymes and Cofactors

inferredcites →https://doi.org/10.1039/c2sc20098hopenalex-snapshot

Poly(disulfide)s

inferredcites →https://doi.org/10.1039/c5py01005eopenalex-snapshot

Lipoates as building blocks of sulfur-containing branched macromolecules

inferredcites →https://doi.org/10.1039/tf9575300813openalex-snapshot

The polymerization of 1-oxa-4:5 dithio-cycloheptane

inferredcites →https://doi.org/10.1080/01961779008048732openalex-snapshot

Naturally Occurring 1,2-Dithiolanes and 1,2,3-Trithianes. Chemical and Biological Properties

inferredcites →https://doi.org/10.1080/15321797208068172openalex-snapshot

Thermodynamics of Polymerization. IV. Thermodynamics of Equilibrium Polymerization

inferredcites →https://doi.org/10.1080/15583726908545926openalex-snapshot

Thermodynamics of Polymerization. I

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OBSERVATIONS OF C‐S AND S‐S BOND CLEAVAGE IN THE PHOTOLYSIS OF DISULFIDES IN SOLUTION

inferredcites →https://doi.org/10.1295/kobunshi.39.378openalex-snapshot

Thermodynamics of polymerization.

inferredcites →https://doi.org/10.1295/polymj.37.512openalex-snapshot

Thermal Polymerization of 1,2-Dithiane

inferredcites →https://doi.org/10.2172/915447openalex-snapshot

Thioctic Acid: Physics, Chemistry, and Biology

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