Crystallization-Driven Self-Assembly of Coil–Comb-Shaped Polypeptoid Block Copolymers: Solution Morphology and Self-Assembly Pathways
Abstract
Crystallization-driven self-assembly (CDSA) of amphiphilic polymers into well-defined nanoscopic structures with different morphologies and functionalities has attracted increasing attention. Here, we investigate the CDSA of coil–comb-shaped diblock copolypeptoids, namely, poly(N-methyl glycine)-b-poly(N-decyl glycine) (PNMG-b-PNDG), in dilute methanol solution using X-ray/neutron solution scattering in conjunction with cryogenic transmission electron microscopy techniques. A series of PNMG-b-PNDGs were synthesized by sequential benzyl amine-initiated ring-opening polymerizations of the corresponding N-substituted N-carboxyanhydrides, in which the degree of polymerization and the length of the blocks were varied. The PNMG-b-PNDG polymers with a lower volume fraction of the crystalline PNDG blocks (fPNDG = 0.44) were found to slowly self-assemble into one-dimensional long wormlike nanofibrils in methanol. The nanofibrils bear an anisotropic crystalline core where the comb-shaped PNDG blocks were stacked in a face-to-face fashion along the long axis of the nanofibrils. Upon increasing fPNDG to 0.61 and 0.68, the final morphology of PNMG-b-PNDG micelles changed from wormlike nanofibrils to rigid short nanorods and then two-dimensional nanosheets. The nanofibrils were formed by a self-seeding growth pathway that involves the initial formation of a few seeded crystals followed by the addition of soluble unimers to the preferred crystal facets resulting in the gradual elongation of the micelles. By contrast, themore »
- Authors:
-
[1];
[2];
[3];
[3];
[1]
- Louisiana State Univ., Baton Rouge, LA (United States)
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
- Tulane Univ., New Orleans, LA (United States)
- Publication Date:
- Research Org.:
- Louisiana State Univ., Baton Rouge, LA (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF); National Institutes of Health (NIH)
- OSTI Identifier:
- 1615946
- Alternate Identifier(s):
- OSTI ID: 1673421
- Grant/Contract Number:
- SC0012432; CHE 1609446; AC02-06CH11357; SC0012704; P41 GM111244; KP1605010; S10 OD012331; DMR-1829070
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Macromolecules
- Additional Journal Information:
- Journal Volume: 52; Journal Issue: 22; Journal ID: ISSN 0024-9297
- Publisher:
- American Chemical Society
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; Nanostructures; Crystallization; Alcohols; Micelles; Nanorods; Nanostructures, Crystallization, Alcohols, Micelles, Nanorods
Citation Formats
Jiang, Naisheng, Yu, Tianyi, Darvish, Omead A., Qian, Shuo, Mkam Tsengam, Igor Kevin, John, Vijay, and Zhang, Donghui. Crystallization-Driven Self-Assembly of Coil–Comb-Shaped Polypeptoid Block Copolymers: Solution Morphology and Self-Assembly Pathways. United States: N. p., 2019.
Web. doi:10.1021/acs.macromol.9b01546.
Jiang, Naisheng, Yu, Tianyi, Darvish, Omead A., Qian, Shuo, Mkam Tsengam, Igor Kevin, John, Vijay, & Zhang, Donghui. Crystallization-Driven Self-Assembly of Coil–Comb-Shaped Polypeptoid Block Copolymers: Solution Morphology and Self-Assembly Pathways. United States. https://doi.org/10.1021/acs.macromol.9b01546
Jiang, Naisheng, Yu, Tianyi, Darvish, Omead A., Qian, Shuo, Mkam Tsengam, Igor Kevin, John, Vijay, and Zhang, Donghui. Tue .
"Crystallization-Driven Self-Assembly of Coil–Comb-Shaped Polypeptoid Block Copolymers: Solution Morphology and Self-Assembly Pathways". United States. https://doi.org/10.1021/acs.macromol.9b01546. https://www.osti.gov/servlets/purl/1615946.
@article{osti_1615946,
title = {Crystallization-Driven Self-Assembly of Coil–Comb-Shaped Polypeptoid Block Copolymers: Solution Morphology and Self-Assembly Pathways},
author = {Jiang, Naisheng and Yu, Tianyi and Darvish, Omead A. and Qian, Shuo and Mkam Tsengam, Igor Kevin and John, Vijay and Zhang, Donghui},
abstractNote = {Crystallization-driven self-assembly (CDSA) of amphiphilic polymers into well-defined nanoscopic structures with different morphologies and functionalities has attracted increasing attention. Here, we investigate the CDSA of coil–comb-shaped diblock copolypeptoids, namely, poly(N-methyl glycine)-b-poly(N-decyl glycine) (PNMG-b-PNDG), in dilute methanol solution using X-ray/neutron solution scattering in conjunction with cryogenic transmission electron microscopy techniques. A series of PNMG-b-PNDGs were synthesized by sequential benzyl amine-initiated ring-opening polymerizations of the corresponding N-substituted N-carboxyanhydrides, in which the degree of polymerization and the length of the blocks were varied. The PNMG-b-PNDG polymers with a lower volume fraction of the crystalline PNDG blocks (fPNDG = 0.44) were found to slowly self-assemble into one-dimensional long wormlike nanofibrils in methanol. The nanofibrils bear an anisotropic crystalline core where the comb-shaped PNDG blocks were stacked in a face-to-face fashion along the long axis of the nanofibrils. Upon increasing fPNDG to 0.61 and 0.68, the final morphology of PNMG-b-PNDG micelles changed from wormlike nanofibrils to rigid short nanorods and then two-dimensional nanosheets. The nanofibrils were formed by a self-seeding growth pathway that involves the initial formation of a few seeded crystals followed by the addition of soluble unimers to the preferred crystal facets resulting in the gradual elongation of the micelles. By contrast, the nanorods were formed by a two-stage process involving the formation of spherical micelles with an amorphous core in the first stage and rapid confined crystallization of the micellar core and their fusion into rodlike nanostructures at the second stage. Understanding the relationship between chemical composition, micellar morphology, and CDSA pathway of coil–comb-shaped diblock copolypeptoids is an important step toward the rational design of anisotropic polymeric nanostructures with tailorable morphology.},
doi = {10.1021/acs.macromol.9b01546},
journal = {Macromolecules},
number = 22,
volume = 52,
place = {United States},
year = {Tue Nov 12 00:00:00 EST 2019},
month = {Tue Nov 12 00:00:00 EST 2019}
}
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