Dispersity control in atom transfer radical polymerizations through addition of phenylhydrazine DOI
Vivek R. Yadav,

Nairah Hashmi,

Wenyue Ding

et al.

Polymer Chemistry, Journal Year: 2018, Volume and Issue: 9(33), P. 4332 - 4342

Published: Jan. 1, 2018

Phenylhydrazine is an effective modifier for conventional ATRP syntheses, providing systematic control over the dispersity of polymers with unimodal molecular weight distributions.

Language: Английский

Rationally designed Ru(ii)-metallacycle chemo-phototheranostic that emits beyond 1000 nm DOI Creative Commons

Chonglu Li,

Yuling Xu, Le Tu

et al.

Chemical Science, Journal Year: 2022, Volume and Issue: 13(22), P. 6541 - 6549

Published: Jan. 1, 2022

Along-wavelength emissive Ru( ii ) metallacycle chemo-phototheranostic was prepared via self-assembly that exhibits excellent photostability, deep-tissue penetration capability, and promising chemo-phototherapeutic performance in vitro vivo .

Language: Английский

Citations

69

Precise Control of Both Dispersity and Molecular Weight Distribution Shape by Polymer Blending DOI Creative Commons
Richard Whitfield, Nghia P. Truong, Athina Anastasaki

et al.

Angewandte Chemie International Edition, Journal Year: 2021, Volume and Issue: 60(35), P. 19383 - 19388

Published: June 16, 2021

The breadth and the shape of molecular weight distributions can significantly influence fundamental polymer properties that are critical for various applications. However, current approaches require extensive synthesis multiple polymers, limited in dispersity precision typically incapable simultaneously controlling both distributions. Here we report a simplified approach, whereby on mixing two polymers (one high Đ one low Đ), any intermediate value be obtained (e.g. from 1.08 to 1.84). Unrivalled is achieved, with values even nearest 0.01 1.37→1.38→1.39→1.40→1.41→1.42→1.43→1.44→1.45), while maintaining fairly monomodal This approach was also employed control obtain diblock copolymers accuracy. straightforward nature our methodology alongside its compatibility wide range polymerisation protocols ATRP, RAFT), expands toolbox tailored polymeric materials makes them accessible all researchers.

Language: Английский

Citations

62

Controlling Dynamics of Associative Networks through Primary Chain Length DOI
Jacob J. Lessard, Kevin A. Stewart, Brent S. Sumerlin

et al.

Macromolecules, Journal Year: 2022, Volume and Issue: 55(22), P. 10052 - 10061

Published: Nov. 2, 2022

Dynamic networks couple the robust nature of thermosets with shapeability and recyclability thermoplastics. Though a wealth exchange chemistries can be leveraged to fabricate dynamic networks, reversibly cross-linked systems that are comprised primarily chains nonexchangeable backbones increase network complexity render flow behavior difficult predict. Here, we report polymethacrylate-based vitrimers prepared by cross-linking β-ketoester-containing polymers multifunctional amines demonstrate molecular weight dispersity primary tuned actively tailor dynamics resulting networks. Vitrimers similar composition cross-link density made from below well above entanglement exhibited distinct viscoelastic properties energies activation ranging 93 264 kJ/mol. Resistance creep increased dramatically increasing chain length. Finally, blending prepolymers skew Mn above/below Me was demonstrated, showing distinguishable effect prepolymer breadth skewness on vitrimer flow. Our results suggest tailoring chain-length distribution is viable strategy design materials predictable customizable behavior.

Language: Английский

Citations

51

Transparent, intrinsically fire-safe yet impact-resistant poly(carbonates-b-siloxanes) containing Schiff-base and naphthalene-sulfonate DOI Creative Commons

Ting Sai,

Xiaodi Ye,

Bingtao Wang

et al.

Journal of Material Science and Technology, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 1, 2024

Language: Английский

Citations

17

Polymer Dispersity Control by Organocatalyzed Living Radical Polymerization DOI
Xu Liu, Chen‐Gang Wang, Atsushi Goto

et al.

Angewandte Chemie International Edition, Journal Year: 2019, Volume and Issue: 58(17), P. 5598 - 5603

Published: Feb. 20, 2019

Molecular weight distribution of polymers, termed dispersity (Đ), is a fundamental parameter for determining polymer material properties. This paper reports novel approach controlling Đ by exploiting temperature-selective radical generation in organocatalyzed living polymerization. The polymers with tailored were synthesized batch system without the assistance an external pump. A unique aspect this that was tuneable from 1.11 to 1.50 any segment diblock, triblock, and multiblock copolymers form star brush segmental or topological restriction. amenable various monomers free metals thus attractive applications. also generated brushes on surfaces Đ. An interesting finding exhibited interaction molecules, depending value.

Language: Английский

Citations

74

Molecular Weight Distribution Shape as a Versatile Approach to Tailoring Block Copolymer Phase Behavior DOI
Dillon T. Gentekos, Brett P. Fors

ACS Macro Letters, Journal Year: 2018, Volume and Issue: 7(6), P. 677 - 682

Published: May 24, 2018

The molecular weight distributions (MWDs) of block copolymers significantly impact their morphological phase behavior, but exploiting these features as a means to tune material properties has been limited the MWD breadth, or dispersity (Đ). Manipulation entire promising potential address this challenge by providing convenient and versatile route toward tailoring polymer nanostructure. Herein, we describe self-assembly poly(styrene)-block-poly(2-vinylpyridine) (PS-b-P2VP) where PS blocks have systematically deviating compositions weights. We find that controlling shape, breadth skew, afforded access different morphologies in samples with same characteristics, including Đ. As such, illustrate generality effectiveness strategy anticipate it will facilitate increased deployment disperse advanced materials applications.

Language: Английский

Citations

71

Recent development in halogen-bonding-catalyzed living radical polymerization DOI Open Access
Chen‐Gang Wang,

Amerlyn Ming Liing Chong,

Houwen Matthew Pan

et al.

Polymer Chemistry, Journal Year: 2020, Volume and Issue: 11(35), P. 5559 - 5571

Published: Jan. 1, 2020

The development and applications of an organocatalyzed living radical polymerization via halogen-bonding catalysis, i.e., reversible complexation mediated (RCMP), are highlighted.

Language: Английский

Citations

60

Predictive design of polymer molecular weight distributions in anionic polymerization DOI
Sergii Domanskyi, Dillon T. Gentekos, Vladimir Privman

et al.

Polymer Chemistry, Journal Year: 2019, Volume and Issue: 11(2), P. 326 - 336

Published: June 13, 2019

Polymer molecular weight distributions are targeted through kinetic modeled with high fidelity based on the temporal control of chain initiation in anionic polymerizations.

Language: Английский

Citations

57

Comprehensive control over molecular weight distributions through automated polymerizations DOI
Maarten Rubens, Tanja Junkers

Polymer Chemistry, Journal Year: 2019, Volume and Issue: 10(46), P. 6315 - 6323

Published: Jan. 1, 2019

Automated synthesis by mixing of individual polymer distributions to tune the shape and properties artificial molecular weight distributions.

Language: Английский

Citations

57

Shifting Boundaries: Controlling Molecular Weight Distribution Shape for Mechanically Enhanced Thermoplastic Elastomers DOI
Stephanie I. Rosenbloom, Brett P. Fors

Macromolecules, Journal Year: 2020, Volume and Issue: 53(17), P. 7479 - 7486

Published: Aug. 24, 2020

Thermoplastic elastomers (TPEs) based on polystyrene (PS) are commonplace in society. The elastomeric properties of these materials often sacrificed to increase mechanical such as stiffness, strength, and toughness. We sought produce stiff, strong, tough TPEs that retain their by shifting the lamellar phase boundary toward higher PS content. By precisely controlling molecular weight distribution (MWD) shape one block polystyrene-block-polyisoprene-block-polystyrene (SIS), we produced continuous at atypically high volume fractions, from 0.33 triblocks with a narrow MWD ∼0.39 broadened block. Furthermore, observed hexagonal/lamellar coexistence fraction 0.39 when first was asymmetric. These exhibit enhanced consistent fractions morphologies.

Language: Английский

Citations

57