SYNTHESIS AND APPLICATION OF MACROCYCLIC AND MACROACYCLIC SCHIFF-BASES

被引:139
作者
GUERRIERO, P
VIGATO, PA
FENTON, DE
HELLIER, PC
机构
[1] CNR,IST CHIM & TECNOL RADIOELEMENTI,CORSO STATI UNIT 4,I-35100 PADUA,ITALY
[2] UNIV SHEFFIELD,DEPT CHEM,SHEFFIELD S3 7HF,S YORKSHIRE,ENGLAND
来源
ACTA CHEMICA SCANDINAVICA | 1992年 / 46卷 / 11期
关键词
D O I
10.3891/acta.chem.scand.46-1025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The challenge presented by the design and synthesis of ligands capable of organising more than two metal centres into a predetermined arrangement in order to develop new materials is discussed. The design and synthesis of macropolycyclic and/or macropolyacyclic Schiff bases, which have the potential to act as metal-specific ligands, or can allow the simultaneous incorporation of two or more metals in well defined homo- or heterodinuclear arrays, is presented together with the role of metal ions as templating devices and the opportunities to utilise transmetallation reactions. Formation of Schiff bases followed by reductive demetallation leads to a variety of more stable, and flexible, ligands useful in metal transfer studies. C- and N-functionalisation of macrocyclic Schiff bases produces pendant-armed ligands which permit a more dynamic complexation of the metal ion than is found in bicyclic ligands.
引用
收藏
页码:1025 / 1046
页数:22
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