A novel chiral terpyridine macrocycle as a fluorescent sensor for enantioselective recognition of amino acid derivatives
Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review
Author(s)
Detail(s)
| Original language | English |
|---|---|
| Pages (from-to) | 384-385 |
| Journal / Publication | Chemical Communications |
| Volume | 10 |
| Issue number | 4 |
| Publication status | Published - 21 Feb 2004 |
Link(s)
Abstract
Terpyridine macrocycle 1 is shown to be a strong chelating agent for organic ammonium salts and also a useful chromophore in fluorescent sensing. It exhibits very good enantioselectivity (Kobs (S)/Kobs (R) = 3.8) in chiral discrimination of α-phenylglycine methyl ester hydrochloride (PhEtOMe).
Citation Format(s)
A novel chiral terpyridine macrocycle as a fluorescent sensor for enantioselective recognition of amino acid derivatives. / Wong, Wing-Leung; Huang, Ka-Hung; Teng, Pang-Fei et al.
In: Chemical Communications, Vol. 10, No. 4, 21.02.2004, p. 384-385.Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review
