Category: 71195-85-2

Das, Anindita; Lin, Shaojian; Theato, Patrick published the artcile< Supramolecularly Cross-Linked Nanogel by Merocyanine Pendent Copolymer>, Electric Literature of 71195-85-2, the main research area is supramolecularly crosslinked nanogel merocyanine pendent polyacrylic.

Directional dipole-dipole interaction mediated antiparallel dimerization of merocyanine dye (MD) has been explored for maneuvering supramol. assembly of MD-conjugated flexible macromols. leading to a cross-linked nanogel. The MD-functionalized copolymer was synthesized by a newly developed organocatalytic transesterification strategy for postpolymn. functionalization of poly(pentafluorophenyl acrylate) (polyPFPA)-based reactive copolymer. Presence of ∼35% pendant MD attached to a coil-like polymer chain leads to spontaneous formation of highly emitting crosslinked nanogel with efficient container property and appreciable stability in toluene owing to strong dimerization propensity among the MD. Considering the significance of MD in the context of nonlinear optics and photovoltaics, these results not only enrich the toolbox for engineering macromol. assembly, but also open up new possibilities for future organic materials.

ACS Macro Letters published new progress about Fluoropolymers Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Electric Literature of 71195-85-2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Brooks, Karson; Razavi, Mir Jalil; White, Evan M.; Wang, Xianqiao; Locklin, Jason published the artcile< The formation and evolution of creased morphologies using reactive diffusion in ultrathin polymer brush platforms>, HPLC of Formula: 71195-85-2, the main research area is creasing ultrathin polymer brush modification reactive diffusion morphol.

Precisely controlling the morphol. in thin film coatings has emerged as an important tool used to tune surface properties in a wide variety of applications. Previously, a method is reported to fabricate nanoscale surface creases with a high degree of control over crease size and shape using microcontact printing to perform post-polymerization modification on reactive polymer brush surfaces. In this work, this approach has been expanded to manipulate crease morphol. in reactive thin films, using only a drop of a reactive, viscous polymer, and crease formation has been investigated with a combination of exptl. observations and computational validations. The effects of various rate constants of the reactive polymer brush scaffold, hydrostatic pressure within the droplet of reactive polymer, diffusion profile, and the evolution of the creased morphologies with reaction time are examined in order to better understand crease formation in ultrathin films.

Advanced Materials Interfaces published new progress about Contact angle. 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, HPLC of Formula: 71195-85-2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Xue, Wenwen; Mutlu, Hatice; Theato, Patrick published the artcile< Post-polymerization modification of polymeric active esters towards TEMPO containing polymers: a systematic study>, Recommanded Product: Perfluorophenyl acrylate, the main research area is acrylic polymer radical functionalization secondary battery cathode.

Organic radical batteries (ORB) are a novel promising class for energy storage, particularly featuring a fast charging capability and extraordinary cycle life. The representative polymer, i.e. poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) (PTMA), is usually synthesized by a post-polymerization oxidation method. As an alternate strategy for developing TEMPO-containing polymers, we focused on the post-polymerization modification of poly(pentafluorophenyl acrylate) and poly(pentafluorophenyl methacrylate) with three different TEMPO nucleophiles by transesterification or amidation reactions. Optimizing the conditions of the post-polymerization functionalization reaction by varying different parameters, such as the type of nucleophile, catalyst and solvent, the feeding ratios of catalysts and nucleophiles, along with reaction time and temperatures, resulted in structurally distinct TEMPO containing polymers with varying backbone composition Intriguingly, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl acrylamide) revealed the highest degree functionalization with TEMPO (96.2%) within 3 h. under considerably mild conditions, while poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methylmethacrylamide) exhibited the lowest TEMPO content owing to the steric hindrance from Me group on both the methacrylate chain and the TEMPO derivative All other four TEMPO containing polymers had a radical content similar to PTMA (66.6%) synthesized by the post-oxidation methodol. Noteworthy, compared to TEA (trimethylamine), DMAP (4-dimethylaminopyridine) facilitated an efficient ester bond cleavage independent of the polymer precursor, thus, side reactions such as hydrolysis were increased. Though hydrolysis side reaction occurred, the resulting carboxylic acid group was proven to accelerate ion transfer in a certain way during the redox process. Furthermore, due to the higher TEMPO content, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl acrylamide) exhibited a 12-22 mAh/g higher specific capacity compared to the PTMA-oxidation when running at 5C for 500 cycles.

European Polymer Journal published new progress about Battery capacity. 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Recommanded Product: Perfluorophenyl acrylate.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Suga, Takeo; Aoki, Kohei; Yashiro, Toshiaki; Nishide, Hiroyuki published the artcile< ""Click"" Incorporation of Radical/Ionic Sites into a Reactive Block Copolymer: A Facile and On-Demand Domain Functionalization Approach toward Organic Resistive Memory>, Product Details of C9H3F5O2, the main research area is Click amidation radical ionic reactive block copolymer resistive memory; charge-transport; ionic polymer; nitroxide radical; organic electronics; postpolymerization modification.

Reversible addition-fragmentation chain transfer polymerization yields reactive block copolymers bearing the pentafluorophenyl ester (PFPA) group, and subsequent Click amidation using 2,2,6,6-tetramethylpiperidine-N-oxyl- and imidazolium-functionalized primary amines produces the corresponding functional block copolymers, leading to installation of statistical radical- and ionic sites into the PFPA segment. The monolayered thin film devices fabricated using the obtained block copolymers exhibit repeatable switching of elec. conductivity (on/off ratio > 103) under a bias voltage, which reveals that the coexistence of radicals and ions in the same spherical domain of the copolymer layer is a prerequisite for repeatable switching memory.

Macromolecular Rapid Communications published new progress about Amidation. 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Product Details of C9H3F5O2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

zur Borg, Lisa; Lee, Donggu; Lim, Jaehoon; Bae, Wan Ki; Park, Myeongjin; Lee, Seonghoon; Lee, Changhee; Char, Kookheon; Zentel, Rudolf published the artcile< The effect of band gap alignment on the hole transport from semiconducting block copolymers to quantum dots>, Reference of 71195-85-2, the main research area is bandgap alignment hole transport semiconducting copolymer quantum dot LED.

Semiconducting hole transporting block copolymers were chem. modified to adjust their energy levels to that of CdSe/CdS/CdZnS red quantum dots. Hybrids with optimized energy levels could be used to build strongly improved quantum dot based LEDs (QLEDs).

Journal of Materials Chemistry C: Materials for Optical and Electronic Devices published new progress about Band gap. 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Reference of 71195-85-2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Garcia, Edzna S.; Xiong, Thao M.; Lifschitz, Abygail; Zimmerman, Steven C. published the artcile< Tandem catalysis using an enzyme and a polymeric ruthenium-based artificial metalloenzyme>, Application In Synthesis of 71195-85-2, the main research area is tandem catalysis polymeric ruthenium catalyst.

A Ru-containing single chain nanoparticle (SCNP) was prepared in three steps using radical polymerization of pentafluorophenylacrylate, post-polymerization functionalization with three different alkylamines, and coordination of Ru. The polymer was characterized by 1H NMR, 19F NMR, UV-vis, and DLS. The catalytic activity of the Ru-SCNP for Ru-catalyzed cleavage of allylcarbamates was evaluated by fluorescence spectroscopy and a higher percent conversion and initial rate of reaction was observed when compared to that of the free catalyst in buffer and cell media. The catalytic SCNP was also shown to perform tandem catalysis with β-galactosidase.

Polymer Chemistry published new progress about Acrylic polymers, fluorine-containing Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Application In Synthesis of 71195-85-2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Das, Anindita; Lin, Shaojian; Theato, Patrick published the artcile< Supramolecularly Cross-Linked Nanogel by Merocyanine Pendent Copolymer>, Electric Literature of 71195-85-2, the main research area is supramolecularly crosslinked nanogel merocyanine pendent polyacrylic.

Directional dipole-dipole interaction mediated antiparallel dimerization of merocyanine dye (MD) has been explored for maneuvering supramol. assembly of MD-conjugated flexible macromols. leading to a cross-linked nanogel. The MD-functionalized copolymer was synthesized by a newly developed organocatalytic transesterification strategy for postpolymn. functionalization of poly(pentafluorophenyl acrylate) (polyPFPA)-based reactive copolymer. Presence of ∼35% pendant MD attached to a coil-like polymer chain leads to spontaneous formation of highly emitting crosslinked nanogel with efficient container property and appreciable stability in toluene owing to strong dimerization propensity among the MD. Considering the significance of MD in the context of nonlinear optics and photovoltaics, these results not only enrich the toolbox for engineering macromol. assembly, but also open up new possibilities for future organic materials.

ACS Macro Letters published new progress about Fluoropolymers Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Electric Literature of 71195-85-2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Brooks, Karson; Razavi, Mir Jalil; White, Evan M.; Wang, Xianqiao; Locklin, Jason published the artcile< The formation and evolution of creased morphologies using reactive diffusion in ultrathin polymer brush platforms>, HPLC of Formula: 71195-85-2, the main research area is creasing ultrathin polymer brush modification reactive diffusion morphol.

Precisely controlling the morphol. in thin film coatings has emerged as an important tool used to tune surface properties in a wide variety of applications. Previously, a method is reported to fabricate nanoscale surface creases with a high degree of control over crease size and shape using microcontact printing to perform post-polymerization modification on reactive polymer brush surfaces. In this work, this approach has been expanded to manipulate crease morphol. in reactive thin films, using only a drop of a reactive, viscous polymer, and crease formation has been investigated with a combination of exptl. observations and computational validations. The effects of various rate constants of the reactive polymer brush scaffold, hydrostatic pressure within the droplet of reactive polymer, diffusion profile, and the evolution of the creased morphologies with reaction time are examined in order to better understand crease formation in ultrathin films.

Advanced Materials Interfaces published new progress about Contact angle. 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, HPLC of Formula: 71195-85-2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Xue, Wenwen; Mutlu, Hatice; Theato, Patrick published the artcile< Post-polymerization modification of polymeric active esters towards TEMPO containing polymers: a systematic study>, Recommanded Product: Perfluorophenyl acrylate, the main research area is acrylic polymer radical functionalization secondary battery cathode.

Organic radical batteries (ORB) are a novel promising class for energy storage, particularly featuring a fast charging capability and extraordinary cycle life. The representative polymer, i.e. poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) (PTMA), is usually synthesized by a post-polymerization oxidation method. As an alternate strategy for developing TEMPO-containing polymers, we focused on the post-polymerization modification of poly(pentafluorophenyl acrylate) and poly(pentafluorophenyl methacrylate) with three different TEMPO nucleophiles by transesterification or amidation reactions. Optimizing the conditions of the post-polymerization functionalization reaction by varying different parameters, such as the type of nucleophile, catalyst and solvent, the feeding ratios of catalysts and nucleophiles, along with reaction time and temperatures, resulted in structurally distinct TEMPO containing polymers with varying backbone composition Intriguingly, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl acrylamide) revealed the highest degree functionalization with TEMPO (96.2%) within 3 h. under considerably mild conditions, while poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methylmethacrylamide) exhibited the lowest TEMPO content owing to the steric hindrance from Me group on both the methacrylate chain and the TEMPO derivative All other four TEMPO containing polymers had a radical content similar to PTMA (66.6%) synthesized by the post-oxidation methodol. Noteworthy, compared to TEA (trimethylamine), DMAP (4-dimethylaminopyridine) facilitated an efficient ester bond cleavage independent of the polymer precursor, thus, side reactions such as hydrolysis were increased. Though hydrolysis side reaction occurred, the resulting carboxylic acid group was proven to accelerate ion transfer in a certain way during the redox process. Furthermore, due to the higher TEMPO content, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl acrylamide) exhibited a 12-22 mAh/g higher specific capacity compared to the PTMA-oxidation when running at 5C for 500 cycles.

European Polymer Journal published new progress about Battery capacity. 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Recommanded Product: Perfluorophenyl acrylate.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Suga, Takeo; Aoki, Kohei; Yashiro, Toshiaki; Nishide, Hiroyuki published the artcile< ""Click"" Incorporation of Radical/Ionic Sites into a Reactive Block Copolymer: A Facile and On-Demand Domain Functionalization Approach toward Organic Resistive Memory>, Product Details of C9H3F5O2, the main research area is Click amidation radical ionic reactive block copolymer resistive memory; charge-transport; ionic polymer; nitroxide radical; organic electronics; postpolymerization modification.

Reversible addition-fragmentation chain transfer polymerization yields reactive block copolymers bearing the pentafluorophenyl ester (PFPA) group, and subsequent Click amidation using 2,2,6,6-tetramethylpiperidine-N-oxyl- and imidazolium-functionalized primary amines produces the corresponding functional block copolymers, leading to installation of statistical radical- and ionic sites into the PFPA segment. The monolayered thin film devices fabricated using the obtained block copolymers exhibit repeatable switching of elec. conductivity (on/off ratio > 103) under a bias voltage, which reveals that the coexistence of radicals and ions in the same spherical domain of the copolymer layer is a prerequisite for repeatable switching memory.

Macromolecular Rapid Communications published new progress about Amidation. 71195-85-2 belongs to class esters-buliding-blocks, and the molecular formula is C9H3F5O2, Product Details of C9H3F5O2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics