Effect of H-Bonding on Order Amplification in the Growth of a Supramolecular Polymer in Water.

While a great deal of knowledge on the roles of hydrogen bonding and hydrophobicity in proteins have resulted in the creation of rationally designed and functional peptidic structures, the roles of these forces on purely synthetic supramolecular architectures in water have proven difficult to ascertain. Focusing on a 1,3,5-benzenetricarboxamide (BTA) based supramolecular polymer, we have designed a molecular modeling strategy to dissect the energetic contributions involved in the self-assembly (electrostatic, hydrophobic, etc.) upon growth of both ordered BTA stacks and random BTA aggregates. Utilizing this set of simulations, we have unraveled the cooperative mechanism for polymer growth, where a critical size must be reached in the aggregates before emergence and amplification of order into the experimentally observed fibers. Furthermore, we have found that the formation of ordered fibers is favored over disordered aggregates solely on the base of electrostatic interactions. Detailed analysis of the simulation data suggests that H-bonding is a major source of this stabilization energy. Experimental and computational comparison with a newly synthesized 1,3,5-benzenetricarboxyester (BTE) derivative, lacking the ability to form the H-bonding network, demonstrated that this BTE variant is also capable of fiber formation, albeit at a reduced persistence length. This work provides unambiguous ev-idence for the key 1D driving force of hydrogen bonding in enhancing the persistency of monomer stacking and amplifying the lev-el of order into the growing supramolecular polymer in water. Our computational approach provides an important relationship di-rectly linking the structure of the monomer to the structure and properties of the supramolecular polymer.