TY - JOUR
T1 - A Block Supramolecular Polymer and Its Kinetically Enhanced Stability
AU - Jung, Sung Ho
AU - Bochicchio, Davide
AU - Pavan, Giovanni M.
AU - Takeuchi, Masayuki
AU - Sugiyasu, Kazunori
N1 - Funding Information:
This work was supported by KAKENHI (JP15H05483 for K.S.) Scientific Research on Innovative Areas Dynamical ordering of biomolecular systems for creation of integrated functions (JP16H00787), pi;-System figuration: control of electronand structural dynamism for innovative functions (JP26102009 for M.T.), and the Nanotechnology Network Project from the Ministry of Education, Culture, Sports, Science and Technology, Japan. S.H.J. thanks the Japan Society for the Promotion of Science (JSPS) for a postdoctoral fellowship for overseas researchers (16F16043). D.B. and G.M.P. acknowledge the Swiss National Science Foundation (SNSF grant 200021-175735 to G.M.P.).
Publisher Copyright:
Copyright © 2018 American Chemical Society.
PY - 2018/8/22
Y1 - 2018/8/22
N2 - Biomolecular systems serve as an inspiration for the creation of multicomponent synthetic supramolecular systems that can be utilized to develop functional materials with complexity. However, supramolecular systems rapidly reach an equilibrium state through dynamic and reversible noncovalent bonds, resulting in a disorganized mixture of components rather than a system in which individual components function cooperatively and/or independently. Thus, efficient synthetic strategies and characterization methods for intricate multicomponent supramolecular assemblies need to be developed. Herein, we report the synthesis of porphyrin-based supramolecular polymers (SPs) in which two distinct block segments consisting of different metal porphyrins are connected: i.e., block supramolecular polymers (BSPs). BSPs with a controlled length and narrow polydispersity were achieved through seeded-growth by a solvent mixing protocol. Interestingly, the block structure permitted the SP as an inner block to coexist with a reagent that was otherwise incompatible with the SP alone. We infer that the inner SP block is compartmentalized in the block structure and endowed with the kinetic stability. Molecular simulations revealed that monomer exchange occurs from the termini of the SP, which corroborated the enhanced stability of the BSP. These results are expected to pave the way for the design of more complex multicomponent supramolecular systems.
AB - Biomolecular systems serve as an inspiration for the creation of multicomponent synthetic supramolecular systems that can be utilized to develop functional materials with complexity. However, supramolecular systems rapidly reach an equilibrium state through dynamic and reversible noncovalent bonds, resulting in a disorganized mixture of components rather than a system in which individual components function cooperatively and/or independently. Thus, efficient synthetic strategies and characterization methods for intricate multicomponent supramolecular assemblies need to be developed. Herein, we report the synthesis of porphyrin-based supramolecular polymers (SPs) in which two distinct block segments consisting of different metal porphyrins are connected: i.e., block supramolecular polymers (BSPs). BSPs with a controlled length and narrow polydispersity were achieved through seeded-growth by a solvent mixing protocol. Interestingly, the block structure permitted the SP as an inner block to coexist with a reagent that was otherwise incompatible with the SP alone. We infer that the inner SP block is compartmentalized in the block structure and endowed with the kinetic stability. Molecular simulations revealed that monomer exchange occurs from the termini of the SP, which corroborated the enhanced stability of the BSP. These results are expected to pave the way for the design of more complex multicomponent supramolecular systems.
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U2 - 10.1021/jacs.8b06016
DO - 10.1021/jacs.8b06016
M3 - Article
C2 - 30056699
AN - SCOPUS:85051979170
SN - 0002-7863
VL - 140
SP - 10570
EP - 10577
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 33
ER -