H-bonding, shape complementarity, and quasi-equivalence are widely accepted as some of the most influential molecular recognition events mediating biological and synthetic self-organizations. H-bonds are weaker than ionic but stronger than van der Waals forces. However, the directionality of H-bonds makes them the most powerful among all nonbonding interactions. Here, we selected two taper-shaped self-assembling dendrons, one flexible and one rigid, and equipped them with -COCH, -CHOH, and -COOH at their apex. They demonstrated the hierarchical way in which shape-complementarity in the presence of -COCH mediated highly ordered helical self-organization for the case of the rigid building block and less ordered helical arrays for the flexible one. Weak H-bonding by -CHOH unwound the helix from the rigid dendron, yielding a porous column. Due to its quasi-equivalence, the flexible dendron tolerated better the H-bonding by -CHOH self-organizing a different helical column. The rigid and the flexible dendrons yielded only disorganized nonhelical columns in the presence of -COOH at the apex. This balance between rigidity, flexibility, and tolerance or lack of it to diverse H-bonding architectures indicates that mechanistic elucidation of the self-organization process helps endow it with the same building block, both helical organizations approaching biological precision, and disorganized nonhelical arrangements.
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http://dx.doi.org/10.1021/jacs.4c10958 | DOI Listing |
Polymers (Basel)
December 2024
Department of Chemistry and Industrial Chemistry, University of Pisa, Via G. Moruzzi 13, 56124 Pisa, Italy.
The elastic response of chromium-tanned leather was successfully improved by treatment with XSBR, a carboxylated styrene-butadiene copolymer. The carboxylic groups pending from a styrene-butadiene rubber (SBR) backbone were found to promote penetration of the aqueous polymer dispersion into the fibrous tanned leather and participated in pH-reversible physical crosslinking by H-bonding. The different penetrations of XSBR or SBR were investigated using a micro-FTIR cross-sectional analysis from the grain (outer) to the flesh (inner) side of 18 wt% elastomer-treated samples, based on the shaved leather weight.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Adaptive Supramolecular Nanosystems Group, University of Montpellier, Institut Européen des Membranes, ENSCM-CNRS, UMR5635, Place E. Bataillon CC047, Montpellier 34095, France.
Aquaporins (AQPs) are natural proteins that can selectively transport water across cell membranes. Heterogeneous H-bonding of water with the inner wall of the pores of AQPs is of maximal importance regarding the optimal stabilization of water clusters within channels, leading to selective pore flow water transport against ions. To gain deeper insight into the water permeation mechanisms, simpler artificial water channels (AWCs) have been developed.
View Article and Find Full Text PDFChem Asian J
December 2024
Department of Pure and Applied Sciences, University of Urbino Carlo Bo, via Ca' le Suore 2-4, 61029, Urbino, Italy.
The synthesis and characterization of a novel bis-urea-based cage receptor for anions (3S,15S)-3,15,20,25-tetramethyl-1,4,6,12,14,17,20,25-octaazatricyclo[15.5.5.
View Article and Find Full Text PDFChem Commun (Camb)
November 2024
Chemical Biology/Genomics Laboratory, Department of Chemistry, Indian Institute of Technology Guwahati, 781039, India.
Decorating biomolecular building blocks, such as amino acids, to afford desired and tuneable photophysical/biophysical properties would allow chemical biologists to use them for several biotechnological and biosensing applications. While many synthetic methodologies have been explored in this direction, advantages provided by click-derived triazole moieties are second to none. However, since their discovery, click-mediated triazoles have been majorly utilised as linkers for conjugating biomolecules, creating materials with novel properties, such as polymers or drug conjugates.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Shanghai Key Lab of Chemical Assessment and Sustainability, School of Chemical Science and Engineering, Tongji University, Shanghai, 200092, P. R. China.
Multiple redox-active amphoteric organics with more n-p fused electron transfer is an ongoing pursuit for superior zinc-organic batteries (ZOBs). Here we report multi-heterocycle-site donor-acceptor conjugated amphoteric organic superstructures (AOSs) by integrating three-electron-accepting n-type triazine motifs and dual-electron-donating p-type piperazine units via H-bonding and π-π stacking. AOSs expose flower-shaped N-heteromacrocyclic electron delocalization topologies to promise full accessibility of built-in n-p redox-active motifs with an ultralow activation energy, thus liberating superior capacity (465 mAh g) for Zn||AOSs battery.
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