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Functionalization-Induced Self-Assembly of Block Copolymers for Nanoparticle Synthesis
Journal article

Functionalization-Induced Self-Assembly of Block Copolymers for Nanoparticle Synthesis

David H. Howe, James L. Hart, Riki M. McDaniel, Mitra L. Taheri and Andrew J. D. Magenau
ACS macro letters, v 7(12), pp 1503-1508
01 Dec 2018
DOI: https://doi.org/10.1021/acsmacrolett.8b00815
PMID: 35651226

Abstract

Physical Sciences Polymer Science Science & Technology
Nanoparticle synthesis was demonstrated via functionalization-induced self-assembly (FISA) of block copolymers using Suzuki-Miyaura cross-coupling. In situ self-assembly was triggered in organic media by the progressive installation of solvophobic pendant groups onto an initially soluble diblock copolymer, rendering the reactive block insoluble and causing the formation of spherical polymeric micelles. Self-assembly was found to depend on the percent functionalization (f(%)), where after a critical threshold micelles were accessible that increased in size with increasing f(%) values. We found the chemical nature of the installed functional group to be crucial for conducting FISA and for controlling the solution morphology, with relatively solvophilic adducts remaining as unimers and increasingly solvophobic adducts trending toward larger micelles, from ca. 40 to 100 nm in diameter. The core and corona of the anticipated micellar structure were visualized using fluorine mapping through electron energy loss spectroscopy, in conjunction with FISA achieved through pendent trifluorophenyl functionality. This work establishes FISA as a new, versatile synthetic strategy to create nanoparticles having tunable morphologies with potential application as molecular payload delivery vehicles.

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Polymer Science
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