TY - JOUR
T1 - Controllable synthesis of patchy particles with tunable geometry and orthogonal chemistry
AU - Chang, Fuqiang
AU - Ouhajji, Samia
AU - Townsend, Alice
AU - Sanogo Lacina, Kanvaly
AU - van Ravensteijn, Bas G.P.
AU - Kegel, Willem K.
N1 - Funding Information:
We acknowledge funding from the China Scholarship Council (CSC no. 201406230043 ). B. G. P. v. R acknowledges the Marie Curie Research Grants Scheme (Grant 838585 – STAR Polymers) for financial support.
Publisher Copyright:
© 2020 The Author(s)
PY - 2021/1/15
Y1 - 2021/1/15
N2 - Hypothesis: Self-assembly using anisotropic colloidal building blocks may lead to superstructures similar to those found in molecular systems yet can have unique optical, electronic, and structural properties. To widen the spectrum of achievable superstructures and related properties, significant effort was devoted to the synthesis of new types of colloidal particles. Despite these efforts, the preparation of anisotropic colloids carrying chemically orthogonal anchor groups on distinct surface patches remains an elusive challenge. Experiments: We report a simple yet effective method for synthesizing patchy particles via seed-mediated heterogeneous nucleation. Key to this procedure is the use of 3-(trimethoxysilyl)propyl methacrylate (TPM) or 3-(trimethoxysilyl)propyl acrylate (TMSPA), which can form patches on a variety of functional polymer seeds via a nucleation and growth mechanism. Findings: A family of anisotropic colloids with tunable numbers of patches and patch arrangements were prepared. By continuously feeding TPM or TMSPA the geometry of the colloids could be adjusted accurately. Furthermore, the patches could be reshaped by selectively polymerizing and/or solvating the individual colloidal compartments. Relying on the chemically distinct properties of the TPM/TMSPA and seed-derived domains, both types of patches could be functionalized independently. Combining detailed control over the patch chemistry and geometry opens new avenues for colloidal self-assembly.
AB - Hypothesis: Self-assembly using anisotropic colloidal building blocks may lead to superstructures similar to those found in molecular systems yet can have unique optical, electronic, and structural properties. To widen the spectrum of achievable superstructures and related properties, significant effort was devoted to the synthesis of new types of colloidal particles. Despite these efforts, the preparation of anisotropic colloids carrying chemically orthogonal anchor groups on distinct surface patches remains an elusive challenge. Experiments: We report a simple yet effective method for synthesizing patchy particles via seed-mediated heterogeneous nucleation. Key to this procedure is the use of 3-(trimethoxysilyl)propyl methacrylate (TPM) or 3-(trimethoxysilyl)propyl acrylate (TMSPA), which can form patches on a variety of functional polymer seeds via a nucleation and growth mechanism. Findings: A family of anisotropic colloids with tunable numbers of patches and patch arrangements were prepared. By continuously feeding TPM or TMSPA the geometry of the colloids could be adjusted accurately. Furthermore, the patches could be reshaped by selectively polymerizing and/or solvating the individual colloidal compartments. Relying on the chemically distinct properties of the TPM/TMSPA and seed-derived domains, both types of patches could be functionalized independently. Combining detailed control over the patch chemistry and geometry opens new avenues for colloidal self-assembly.
KW - Anisotropic colloids
KW - Colloidal molecules
KW - Heterogeneous nucleation
KW - Orthogonal chemistry
KW - Patchy particles
UR - http://www.scopus.com/inward/record.url?scp=85089468386&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2020.08.038
DO - 10.1016/j.jcis.2020.08.038
M3 - Article
C2 - 32827958
AN - SCOPUS:85089468386
SN - 0021-9797
VL - 582
SP - 333
EP - 341
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
IS - Part A
ER -