TY - JOUR
T1 - Rapid Generation of Block Copolymer Libraries Using Automated Chromatographic Separation
AU - Zhang, Cheng
AU - Bates, Morgan W.
AU - Geng, Zhishuai
AU - Levi, Adam E.
AU - Vigil, Daniel
AU - Barbon, Stephanie M.
AU - Loman, Tessa
AU - Delaney, Kris T.
AU - Fredrickson, Glenn H.
AU - Bates, Christopher M.
AU - Whittaker, Andrew K.
AU - Hawker, Craig J.
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/5/27
Y1 - 2020/5/27
N2 - A versatile and scalable strategy is reported for the rapid generation of block copolymer libraries spanning a wide range of compositions starting from a single parent copolymer. This strategy employs automated and operationally simple chromatographic separation that is demonstrated to be applicable to a variety of block copolymer chemistries on multigram scales with excellent mass recovery. The corresponding phase diagrams exhibit increased compositional resolution compared to those traditionally constructed via multiple, individual block copolymer syntheses. Increased uniformity and lower dispersity of the chromatographic libraries lead to differences in the location of order-order transitions and observable morphologies, highlighting the influence of dispersity on the self-assembly of block copolymers. Significantly, this separation technique greatly simplifies the exploration of block copolymer phase space across a range of compositions, monomer pairs, and molecular weights (up to 50000 amu), producing materials with increased control and homogeneity when compared to conventional strategies.
AB - A versatile and scalable strategy is reported for the rapid generation of block copolymer libraries spanning a wide range of compositions starting from a single parent copolymer. This strategy employs automated and operationally simple chromatographic separation that is demonstrated to be applicable to a variety of block copolymer chemistries on multigram scales with excellent mass recovery. The corresponding phase diagrams exhibit increased compositional resolution compared to those traditionally constructed via multiple, individual block copolymer syntheses. Increased uniformity and lower dispersity of the chromatographic libraries lead to differences in the location of order-order transitions and observable morphologies, highlighting the influence of dispersity on the self-assembly of block copolymers. Significantly, this separation technique greatly simplifies the exploration of block copolymer phase space across a range of compositions, monomer pairs, and molecular weights (up to 50000 amu), producing materials with increased control and homogeneity when compared to conventional strategies.
UR - http://www.scopus.com/inward/record.url?scp=85085899992&partnerID=8YFLogxK
U2 - 10.1021/jacs.0c04028
DO - 10.1021/jacs.0c04028
M3 - Article
C2 - 32421319
AN - SCOPUS:85085899992
SN - 0002-7863
VL - 142
SP - 9843
EP - 9849
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 21
ER -