TY - JOUR
T1 - Polymorphism in benzene-1,3,5-tricarboxamide supramolecular assemblies in water
T2 - a subtle trade-off between structure and dynamics
AU - Matsumoto, Nicholas M.
AU - Lafleur, René P.M.
AU - Lou, Xianwen
AU - Shih, Kuo Chih
AU - Wijnands, Sjors P.W.
AU - Guibert, Clément
AU - van Rosendaal, Johannes W.A.M.
AU - Voets, Ilja K.
AU - Palmans, Anja R.A.
AU - Lin, Yao
AU - Meijer, E. W.
PY - 2018/10/17
Y1 - 2018/10/17
N2 - In biology, polymorphism is a well-known phenomenon by which a discrete biomacromolecule can adopt multiple specific conformations in response to its environment. The controlled incorporation of polymorphism into noncovalent aqueous assemblies of synthetic small molecules is an important step toward the development of bioinspired responsive materials. Herein, we report on a family of carboxylic acid functionalized water-soluble benzene-1,3,5-tricarboxamides (BTAs) that self-assemble in water to form one-dimensional fibers, membranes, and hollow nanotubes. Interestingly, one of the BTAs with the optimized position of the carboxylic group in the hydrophobic domain yields nanotubes that undergo reversible temperature-dependent dynamic reorganizations. SAXS and Cryo-TEM data show the formation of elongated, well-ordered nanotubes at elevated temperatures. At these temperatures, increased dynamics, as measured by hydrogen-deuterium exchange, provide enough flexibility to the system to form well-defined nanotube structures with apparently defect-free tube walls. Without this flexibility, the assemblies are frozen into a variety of structures that are very similar at the supramolecular level, but less defined at the mesoscopic level.
AB - In biology, polymorphism is a well-known phenomenon by which a discrete biomacromolecule can adopt multiple specific conformations in response to its environment. The controlled incorporation of polymorphism into noncovalent aqueous assemblies of synthetic small molecules is an important step toward the development of bioinspired responsive materials. Herein, we report on a family of carboxylic acid functionalized water-soluble benzene-1,3,5-tricarboxamides (BTAs) that self-assemble in water to form one-dimensional fibers, membranes, and hollow nanotubes. Interestingly, one of the BTAs with the optimized position of the carboxylic group in the hydrophobic domain yields nanotubes that undergo reversible temperature-dependent dynamic reorganizations. SAXS and Cryo-TEM data show the formation of elongated, well-ordered nanotubes at elevated temperatures. At these temperatures, increased dynamics, as measured by hydrogen-deuterium exchange, provide enough flexibility to the system to form well-defined nanotube structures with apparently defect-free tube walls. Without this flexibility, the assemblies are frozen into a variety of structures that are very similar at the supramolecular level, but less defined at the mesoscopic level.
UR - http://www.scopus.com/inward/record.url?scp=85054667670&partnerID=8YFLogxK
U2 - 10.1021/jacs.8b07697
DO - 10.1021/jacs.8b07697
M3 - Article
C2 - 30221520
AN - SCOPUS:85054667670
SN - 0002-7863
VL - 140
SP - 13308
EP - 13316
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 41
ER -