Supramolecular Self-Sorting Networks using Hydrogen-Bonding Motifs was written by Coubrough, Heather M.;van der Lubbe, Stephanie C. C.;Hetherington, Kristina;Minard, Aisling;Pask, Christopher;Howard, Mark J.;Fonseca Guerra, Celia;Wilson, Andrew J.. And the article was included in Chemistry – A European Journal in 2019.Product Details of 1384100-95-1 The following contents are mentioned in the article:
A current objective in supramol. chem. is to mimic the transitions between complex self-sorted systems that represent a hallmark of regulatory function in nature. In this work, a self-sorting network, comprising linear hydrogen motifs, was created. Selecting six hydrogen-bonding motifs capable of both high-fidelity and promiscuous mol. recognition gave rise to a complex self-sorting system, which included motifs capable of both narcissistic and social self-sorting. Examination of the interactions between individual components, exptl. and computationally, provided a rationale for the product distribution during each phase of a cascade. This reasoning holds through up to five sequential additions of six building blocks, resulting in the construction of a biomimetic network in which the presence or absence of different components provides multiple unique pathways to distinct self-sorted configurations. This study involved multiple reactions and reactants, such as 4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1Product Details of 1384100-95-1).
4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Product Details of 1384100-95-1
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem