Multiple Folding Structures Mediated by Metal Coordination of Acyclic Multidentate Ligand

被引：68

作者：

Akine, Shigehisa ^{[1
]}

Morita, Yoko ^{[1
]}

Utsuno, Fumihiko ^{[1
]}

Nabeshima, Tatsuya ^{[1
]}

机构：

[1] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba, Ibaraki 3058571, Japan

来源：

INORGANIC CHEMISTRY | 2009年 / 48卷 / 22期

关键词：

SITE-SELECTIVE TRANSMETALATION; NEAR-INFRARED LUMINESCENCE; SCHIFF-BASE COMPLEXES; COPPER(II)-GADOLINIUM(III) COMPLEXES; ABIOTIC METALLOFOLDAMERS; ABSOLUTE HELICITY; ZINC(II) COMPLEX; SINGLE; TRINUCLEAR; CHELATE;

D O I：

10.1021/ic901372k

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Four kinds of folded structures are formed upon the metal complexation of a bis(N2O2) ligand in which two oxime-type N2O2 chelate ligands are connected by a flexible diethyleneoxy linker. The N2O2 coordination sites are intended for cl-block transition-metal ions, and the diethyleneoxy linker can interact with hard metal cations. Meso double helical, folded Q-shaped, S-shaped helical, and single helical structures were formed depending on the metal combination. The difference in the affinity to metal cations resulted in variation of the folding modes and enabled the structural conversion between the folded structures.

引用

页码：10670 / 10678

页数：9

共 35 条

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