Bulletin of the Chemical Society of Japan p. 2831 - 2836 (1995)
Update date:2022-08-04
Topics:
Sakamoto, Hidefumi
Ishikawa, Junichi
Otomo, Makoto
Dithiazacrown, tetrathiazacrown, and two tetrathiadiazacrown ether derivatives, bearing a phenyl group on each nitrogen atom at the periphery, were synthesized, and the solvent extractions of some transition metal ions with these compounds were carried out using an H2O-1,2-dichloroethane system.All of the thiazacrown compounds employed exhibited Ag+ selectivity, and formed 1:1:1 complexes of Ag+ : ligand : laurate ion as a counter anion to be extracted into a 1,2-dichloroethane solution.The extractabilities (extraction constants, Kex) for Ag+ decreased in the order: 7,16-diphenyltetrathia-7,16-diaza-18-crown-6 (3) (log Kex = 1.18+/-0.13) > 13-phenyltetrathia-13-aza-15-crown-5 (2) (0.75+/-0.09) > 7-phenyldithia-7-aza-9-crown-3 (1) (-0.47+/-0.06)>13, 16-diphenyltetrathia-13,16-diaza-18-crwon-6 (4) (-0.62+/-0.16).
View MoreBaoding City Light Industry And Textiles Imp.& Exp. Corp. Chemical Department.
Contact:86-312-3262436
Address:NO.658 CHAOYANG SOUTH STREET,BAODING CITY HEBEI CHINA
lianyungang jinkang pharmaceutical technology co., ltd.
Contact:008651885445517
Address:Jinshan industrial park, Ganyu county, Lianyungang, Jiangsu Province, 222115, China
Chengdu Aslee Biopharmaceuticals, Inc
Contact:18608018419
Address:Chengdu Aslee Biopharmaceuticals, Inc
Contact:+1 (647) 918 5848
Address:2343 BRIMLEY RD., Suite 250
website:http://www.chinabarton.com
Contact:+86-573-82719618
Address:No. 162 Fumin Road, Honghe Town,
Doi:10.1021/ol048099s
(2004)Doi:10.1002/chem.201702088
(2017)Doi:10.1021/jo981744m
(1998)Doi:10.1016/S0957-4166(99)00374-2
(1999)Doi:10.1016/S0022-328X(00)89761-2
(1969)Doi:10.1002/adsc.201000803
(2011)