Three step vs one pot synthesis and X-ray crystallographic investigation of heptadentate triamide cyclen (1,4,7,10-tetraazacyclododecane) based ligands and some of their lanthanide ion complexes

被引:33
作者
Gunnlaugsson, T [1 ]
Leonard, JP
Mulready, S
Nieuwenhuyzen, M
机构
[1] Univ Dublin Trinity Coll, Dept Chem, Dublin 2, Ireland
[2] Queens Univ Belfast, Sch Chem, Belfast BT9 5AG, Antrim, North Ireland
关键词
supramolecular chemistry; macrocycles; lanthanide ions; cyclen;
D O I
10.1016/j.tet.2003.10.086
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of several lanthanide complexes from the tris alkylated cyclen (1,4,7,10-tetraazacyclododecane) ligands 1 and 2 is described. The syntheses of 1 and 2 were investigated by means of two different synthetic routes (Method 1 and Method 2). The first of these involves the mono protection of cyclen using 4-methoxyphenylsulfonyl chloride, followed by alkylation of the remaining three secondary amines of cyclen, and deprotection using solvated Na(s). Using this approach only 1 was successfully formed. The X-ray crystal structure of the intermediate, 9 and the corresponding La(III) complex, 9.La is presented. The second method involved the direct synthesis of the two ligands in a single step. The X-ray crystallography of the Eu(III) complex of one of these ligands is presented. Whereas, Method 1 yielded the product 1 in high purity, but in low overall yield, Method 2 gave higher yields for both ligands (similar to50% for both). (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:105 / 113
页数:9
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