Effect of N‑Methylation on Dopamine Surface Chemistry
journal contributionposted on 14.05.2022, 13:04 authored by Yejin Kim, Ahrom You, Dahee Kim, Himani Bisht, Yoonji Heo, Daewha Hong, Min Kim, Sung Min Kang
Dopamine (DA) surface chemistry has received significant attention because of its applicability in a wide range of research fields and the ability to graft functional molecules onto numerous solid surfaces. Various DA derivatives have been newly synthesized to identify key factors affecting the coating efficiency and to advance the coating system development. The oxidation of catechol into quinone followed by internal cyclization via the nucleophilic attack of primary amine is crucial for DA-based surface coating. Thus, it is expected that the amine group’s nucleophilicity control directly affects the coating efficiency. However, it has not been systematically investigated, and most studies have been conducted with the focus on the transformation of amines into amides, despite such approaches decreasing the coating efficiency; the nitrogen in amides is less nucleophilic than that in free amines. In this study, we investigated the effect of N-alkylation on dopamine surface chemistry. N,N-Dimethyldopamine (DMDA) was newly synthesized, and the coating efficiency was systematically compared with DA and N-methyldopamine (MDA). DA N-monomethylation improved the coating rate by increasing the nitrogen nucleophilicity, whereas N,N-dimethylation dramatically decreased the DA surface coating property. In addition, MDA remained capable of universal surface coating and secondary reactions using the surface catechols. This study provides opportunities for developing coating materials with advanced functions and an improved coating rate.
Read the peer-reviewed publication
secondary reactions usingreceived significant attentioninternal cyclization viadeveloping coating materialscoating system developmentmda remained capableamine group ’universal surface coatingbased surface coating>- monomethylation improvedimproved coating ratedopamine surface chemistryvarious da derivativesstudy provides opportunitiescoating ratesurface chemistrycoating efficiencysurface catecholsprimary aminemda ).>- methyldopamine>- dimethyldopamine>- alkylationwide rangesystematically comparedresearch fieldsquinone followednucleophilic attacknewly synthesizedless nucleophilicapproaches decreasingadvanced functions>‑ methylation