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Ring-Opening Polymerization of Trimethylene Carbonate Catalyzed by Methanesulfonic Acid: Activated Monomer versus Active Chain End Mechanisms

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What this work says

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

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Simple Approach to Stabilized Micelles Employing Miktoarm Terpolymers and Stereocomplexes with Application in Paclitaxel Delivery

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Organocatalytic Ring-Opening Polymerization

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Triazabicyclodecene: A Simple Bifunctional Organocatalyst for Acyl Transfer and Ring-Opening Polymerization of Cyclic Esters

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Tagging alcohols with cyclic carbonate: a versatile equivalent of (meth)acrylate for ring-opening polymerization

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Polylactones. 16. Cationic Polymerization of Trimethylene Carbonate and Other Cyclic Carbonates

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inferred← citeshttps://doi.org/10.1039/c3py00667kopenalex-snapshot

Imidodiphosphoric acid as a bifunctional catalyst for the controlled ring-opening polymerization of δ-valerolactone and ε-caprolactone

inferred← citeshttps://doi.org/10.1039/c3py00935aopenalex-snapshot

Selective O -acyl ring-opening of β-butyrolactone catalyzed by trifluoromethane sulfonic acid: application to the preparation of well-defined block copolymers

inferred← citeshttps://doi.org/10.1039/c3py01613gopenalex-snapshot

o -Benzenedisulfonimide as a recyclable cationic organocatalyst for the controlled/living ring-opening polymerization of δ-valerolactone and ε-caprolactone

inferred← citeshttps://doi.org/10.1039/c4py00773eopenalex-snapshot

A base–conjugate-acid pair for living/controlled ring-opening polymerization of trimethylene carbonate through hydrogen-bonding bifunctional synergistic catalysis

inferred← citeshttps://doi.org/10.1039/c4ra09579kopenalex-snapshot

2,4-Dinitrobenzenesulfonic acid in an efficient Brønsted acid-catalyzed controlled/living ring-opening polymerization of ε-caprolactone

inferred← citeshttps://doi.org/10.1039/c5dt00458fopenalex-snapshot

P,O-Phosphinophenolate zinc( ii ) species: synthesis, structure and use in the ring-opening polymerization (ROP) of lactide, ε-caprolactone and trimethylene carbonate

inferred← citeshttps://doi.org/10.1039/c5py00533gopenalex-snapshot

Organophosphate-catalyzed bulk ring-opening polymerization as an environmentally benign route leading to block copolyesters, end-functionalized polyesters, and polyester-based polyurethane

inferred← citeshttps://doi.org/10.1039/c5py01315aopenalex-snapshot

Ionic hydrogen bond donor organocatalyst for fast living ring-opening polymerization

inferred← citeshttps://doi.org/10.1039/c5py01635eopenalex-snapshot

Three is company: dual intramolecular hydrogen-bond enabled carboxylic acid active in ring-opening polymerization

inferred← citeshttps://doi.org/10.1039/c5py01843aopenalex-snapshot

Synthesis of high-molecular-weight aliphatic polycarbonates by organo-catalysis

inferred← citeshttps://doi.org/10.1039/c5py01846copenalex-snapshot

Development of polycarbonate-containing block copolymers for thin film self-assembly applications

inferred← citeshttps://doi.org/10.1039/c5py01931aopenalex-snapshot

Tripodal hydrogen bond donor binding with sulfonic acid enables ring-opening polymerization

inferred← citeshttps://doi.org/10.1039/c6py01107aopenalex-snapshot

Traceless switch organocatalysis enables multiblock ring-opening copolymerizations of lactones, carbonates, and lactides: by a one plus one approach in one pot

inferred← citeshttps://doi.org/10.1039/c6py01210hopenalex-snapshot

Polymerization of trimethylene carbonates using organic phosphoric acids

inferred← citeshttps://doi.org/10.1039/c6py01248eopenalex-snapshot

Triethylamine-based catalysts for the melt polymerization of carbonate monomers

inferred← citeshttps://doi.org/10.1039/c7py01195dopenalex-snapshot

Synthesis of cinnamoyl and coumarin functionalized aliphatic polycarbonates

inferred← citeshttps://doi.org/10.1039/c7py01451aopenalex-snapshot

Tunable intramolecular H-bonding promotes benzoic acid activity in polymerization: inspiration from nature

inferred← citeshttps://doi.org/10.1039/c7py01671aopenalex-snapshot

Squaramide and amine binary H-bond organocatalysis in polymerizations of cyclic carbonates, lactones, and lactides

inferred← citeshttps://doi.org/10.1039/c7ra01113jopenalex-snapshot

Ring-opening polymerization of ethylene carbonate: comprehensive structural elucidation by 1D & 2D-NMR techniques, and selectivity analysis

inferred← citeshttps://doi.org/10.1039/c8cc08405jopenalex-snapshot

Ring-opening polymerization of trimethylene carbonate to poly(trimethylene carbonate) diol over a heterogeneous high-temperature calcined CeO 2 catalyst

inferred← citeshttps://doi.org/10.1039/c8dt02614aopenalex-snapshot

Low valent Al( ii )–Al( ii ) catalysts as highly active ε-caprolactone polymerization catalysts: indication of metal cooperativity through DFT studies

inferred← citeshttps://doi.org/10.1039/c8gc01909fopenalex-snapshot

Development of a H 3 PW 12 O 40 /CeO 2 catalyst for bulk ring-opening polymerization of a cyclic carbonate

inferred← citeshttps://doi.org/10.1039/c8gc03607aopenalex-snapshot

Metal-free synthesis of poly(trimethylene carbonate) by efficient valorization of carbon dioxide

inferred← citeshttps://doi.org/10.1039/c8py00835copenalex-snapshot

Hybrid block copolymers of polyesters/polycarbonates and polypeptides synthesized via one-pot sequential ring-opening polymerization

inferred← citeshttps://doi.org/10.1039/c9cs00047jopenalex-snapshot

Advances in the use of CO 2 as a renewable feedstock for the synthesis of polymers

inferred← citeshttps://doi.org/10.1039/d0ra00904kopenalex-snapshot

Formation of cyclic structures in the cationic ring-opening polymerization of 1,3-dioxolane

inferred← citeshttps://doi.org/10.1039/d3tb02793gopenalex-snapshot

Visible light degradable micelles for intraocular corticosteroid delivery

inferred← citeshttps://doi.org/10.1039/d4py00678jopenalex-snapshot

Modular design of a zwitterionic organocatalyst for bulk ring-opening polymerization of cyclic esters

inferred← citeshttps://doi.org/10.1039/d5dt00864fopenalex-snapshot

Shrinking of C–S bonds of organosulfonic acids in superacidic media—investigation of the protonation of methanesulfonic acid and benzenesulfonic acid and their limits

inferred← citeshttps://doi.org/10.1039/d6nj00201copenalex-snapshot

Polycarbonate synthesis via ring-opening polymerization: catalysts, mechanisms, and sustainable strategies

inferred← citeshttps://doi.org/10.1098/rsos.181363openalex-snapshot

Structure and vibrational spectroscopy of methanesulfonic acid

inferred← citeshttps://doi.org/10.1166/mex.2014.1165openalex-snapshot

Cationic ring-opening polymerization of lactones onto chemically modified single layer graphene oxide

inferred← citeshttps://doi.org/10.2478/pjct-2013-0073openalex-snapshot

Investigations on the synthesis and properties of biodegradable poly(ester-carbonate-urea-urethane)s

inferred← citeshttps://doi.org/10.3390/catal12020124openalex-snapshot

En Route to CO2-Based (a)Cyclic Carbonates and Polycarbonates from Alcohols Substrates by Direct and Indirect Approaches

inferred← citeshttps://doi.org/10.3390/coatings13101782openalex-snapshot

Effect of the Presence of a Silane Coupling Agent on Reaction Kinetics of Cationic Thermopolymerization of Epoxy Resin Adhesive

inferred← citeshttps://doi.org/10.3390/pharmaceutics12040338openalex-snapshot

π-π-Stacked Poly(ε-caprolactone)-b-poly(ethylene glycol) Micelles Loaded with a Photosensitizer for Photodynamic Therapy

inferred← citeshttps://doi.org/10.3390/polym11122078openalex-snapshot

DFT Modeling of Organocatalytic Ring-Opening Polymerization of Cyclic Esters: A Crucial Role of Proton Exchange and Hydrogen Bonding

inferred← citeshttps://doi.org/10.3390/polym14102031openalex-snapshot

Overview: Polycarbonates via Ring-Opening Polymerization, Differences between Six- and Five-Membered Cyclic Carbonates: Inspiration for Green Alternatives

inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.71.706openalex-snapshot

Organocatalytic Ring-Opening Polymerization of Cyclic Esters, Cyclic Carbonates, and Epoxides

inferred← citeshttps://doi.org/10.70675/08cdb722zb2c3z46a1za94ezac0385154adbopenalex-snapshot

Polymérisation par ouverture de cycle organocatalysée initiée en surface comme outil de greffage de polymères sur nanocelluloses

inferred← citeshttps://doi.org/10.70675/23773083za3d6z4313zba39zf79b709667d0openalex-snapshot

Synthesis and Properties modulation of novel functional degradable polymers by means of fine tuning of their structure

inferred← citeshttps://doi.org/10.70675/2a463aa8z9d55z4840z8621z38308325a92dopenalex-snapshot

Catalyseurs organiques photolatents pour la polymérisation par ouverture de cycles différée

inferred← citeshttps://doi.org/10.70675/2a475cc6z0bb2z4611zbb30z2a309b5f4523openalex-snapshot

Nanoparticules polymères ciblant le récepteur CXCR3 : élaboration et évaluation sur modèles de tumeur

inferred← citeshttps://doi.org/10.70675/83ab0e6azba83z4631zb20az577f78a9f5e0openalex-snapshot

Copolymères en peigne à greffons éthers et carbonates : du design macromoléculaire à leur utilisation comme électrolyte de batterie au lithium

inferred← citeshttps://doi.org/10.70675/9261d953z2a49z486dzb566zc8b79d47625eopenalex-snapshot

Ingénierie macromoléculaire par ROP organocatalysée : application à l'étude de la nanostructuration de nouveaux copolymères à blocs biodégradables

inferred← citeshttps://doi.org/10.70675/9767ee6dz1a29z4fafz8182z05430216d790openalex-snapshot

Cycloalkenyl macromonomers from new multifunctional inimers : a platform for graft, bottle-brush and mikto-arm star copolymers

inferred← citeshttps://doi.org/10.70675/a1175712zc427z4146zab50z33c719434e17openalex-snapshot

Associations thermoréversibles entre structures multi-bras à base d’oligomères de poly(triméthylène carbonate) pour l’élaboration de matériaux à applications potentielles dans le champ biomédical : relations structures-propriétés

inferred← citeshttps://doi.org/10.70675/a5ad76afz65ddz433bz87cbz8557eff4e7c2openalex-snapshot

Organopolymérisations du méthacrylate de méthyle induites par les carbène N-hétérocycliques et par des paires de Lewis organiques

inferred← citeshttps://doi.org/10.70675/b3eae817z9ef5z4b85z8b71z4af37be33182openalex-snapshot

A nature « copy-paste » approach for an efficient metal-free polymerization route

inferred← citeshttps://doi.org/10.70675/b64899c0zd17ez4161zb39ez4aca7a594041openalex-snapshot

Les acides gras comme source de matériaux polycarbonates aliphatiques originaux

inferred← citeshttps://doi.org/10.70675/ca0b819fzcdbez4e03z8214z78ccd2a9d7daopenalex-snapshot

Disproportionation and ring-opening polymerization of silmethylene-siloxane derivatives

inferred← citeshttps://doi.org/10.70675/fda2da76z5cdcz4f2cz885bzc274cd2c5d39openalex-snapshot

Apport de la farine de maïs plastifiée dans les mélanges à matrice polyester pour des applications films

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