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High‐Performance Liquid Chromatographic Resolution of Neutral and Cationic Hetero[6]Helicenes
Author(s) -
Labrador Geraldine M.,
Bosson Johann,
Breitbach Zachary S.,
Lim Yeeun,
Francotte Eric R.,
Sabia Rocchina,
Villani Claudio,
Armstrong Daniel W.,
Lacour Jérôme
Publication year - 2016
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.22579
Subject(s) - chemistry , cationic polymerization , racemization , enantiomer , aqueous solution , selectivity , resolution (logic) , chromatography , adduct , organic chemistry , catalysis , artificial intelligence , computer science
Cationic hetero[6]helicenes 1 + , 2 + and 3 + have been recently disclosed. Herein we report on their enantiomeric separation using high‐performance liquid chromatography . Separation of the antipodes can be achieved in preparative scale on neutral adducts with Chiralcel OD‐I or Chiralpak ID CSP. Selectivity factors of 1.90, 1.67, and 1.96 were obtained for 1-H , 2-H , and 3-H , respectively. Separation can also be performed on the carbenium ions on regular Chiralpak IA CSP using water‐containing eluents, thus allowing for enantiomeric purity determinations in aqueous environments. Resolution of neutral and cationic helicenes is also achieved on more recently developed LARIHC columns. The versatility of the cyclofructan phases allows for baseline separations for both cases and their loading capabilities are demonstrated. Finally, the configurational stability of 1 + , 2 + , and 3 + was measured. For each replacement of an oxygen atom by an amino group, the racemization barrier increases significantly (Δ G ‡ = 29.8, 36.3 and >37 kcal mol ‐1 for 1 + , 2 + , and 3 + respectively). Chirality 28:282–289, 2016 . © 2016 Wiley Periodicals, Inc.