Self-assembly of metal--polymer analogues of amphiphilic triblock copolymers
ORAL
Abstract
We proposed a block copolymer approach to the self-assembly of inorganic nanrods terminated with polymer molecules at both ends. We organized metal nanorods in structures with varying geometries by using a striking analogy between amphiphilic ABA triblock copolymers and the hydrophilic nanorods tetheredwith hydrophobic polymer chains at both ends. The self-assembly was tunable and reversible and it was achieved solely by changing the solvent quality for the constituent blocks. The distance between adjacent nanorods along chains can be tuned by varying the composition of mixture solvents or the molecular weight of polymer blocks, which allows us precisely control the plasmonic band of self-assembled structures. A systematic study of the self-assembly as a function of solvent composition and the molecular weight of the polymer blocks allowed us to construct a diagram that maps the assembled structures. This approach provides a new route to the organization of anisotropic nanoparticles by using the strategies that are established for the self-assembly of block copolymers.
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Authors
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Zhihong Nie
Department of Chemistry, University of Toronto, Canada
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Daniele Fava
Department of Chemistry, University of Toronto, Canada
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Eugenia Kumacheva
Department of Chemistry, University of Toronto, Canada, University of Toronto
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Shan Zou
Department of Chemistry, University of Toronto, Canada
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Gilbert Walker
Department of Chemistry, University of Toronto, Toronto, ON, M5S 3H6, Canada, Department of Chemistry, University of Toronto, Canada
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Michael Rubinstein
University of North Carolina, Chapel Hill, NC 27599, University of North Carolina, Department of Chemistry, University of North Carolina, USA, Department of Chemistry, University of North Carolina, 27599 Chapel Hill, N.C., USA