Burdinski Dirk, Lub Johan, Pikkemaat Jeroen A, Langereis Sander, Grüll Holger, Ten Hoeve Wolter
Department of Bio-Molecular Engineering, Philips Research, High Tech Campus 11, NL-5656 AE Eindhoven (phone: +31-40-27-48254; fax: +31-40-27-44906).
Department of Materials Analysis, Philips Research, High Tech Campus 11, NL-5656 AE Eindhoven.
Chem Biodivers. 2008 Aug;5(8):1505-1512. doi: 10.1002/cbdv.200890139.
1,4,7,10-Tetrakis{[N-(1H-imidazol-2-yl)carbamoyl]methyl}-1,4,7,10-tetraazacyclododecane (dotami), a tetra(1H-imidazol-2-yl) derivative of the well-studied octadentate 1,4,7,10-tetrakis[(carbamoyl)methyl]-1,4,7,10-tetraazacyclododecane (dotam) ligand, was synthesized by reaction of 1,4,7,10-tetraazacyclododecane with N-(1H-imidazol-2-yl)chloroacetamide in high yield. Its tricationic thulium complex was isolated as a water-soluble chloride salt. The detection of the mildly acidic amide and amine protons by direct proton NMR in aqueous solution was unsuccessful, but such exchangeable protons could be detected via their chemical exchange-dependent saturation transfer (CEST) effect. The observed CEST effect was distinctly different from that found for respective dotam complexes and is, therefore, ascribed to exchangeable protons associated with the imidazole substituent.
1,4,7,10-四{[N-(1H-咪唑-2-基)氨基甲酰基]甲基}-1,4,7,10-四氮杂环十二烷(多他米),是经过充分研究的八齿配体1,4,7,10-四[(氨基甲酰基)甲基]-1,4,7,10-四氮杂环十二烷(多他姆)的四(1H-咪唑-2-基)衍生物,通过1,4,7,10-四氮杂环十二烷与N-(1H-咪唑-2-基)氯乙酰胺反应以高产率合成。其三价铥配合物被分离为水溶性氯化物盐。通过直接质子核磁共振在水溶液中检测弱酸性酰胺和胺质子未成功,但此类可交换质子可通过其化学交换依赖饱和转移(CEST)效应检测到。观察到的CEST效应与相应多他姆配合物的明显不同,因此归因于与咪唑取代基相关的可交换质子。