Terpyridine-Based, Flexible Tripods: From a Highly Symmetric Nanosphere to Temperature-Dependent, Irreversible, 3D Isomeric Macromolecular.Nanocages

被引：58

作者：

Chakraborty, Sourav ^{[1
]}

Hong, Wei ^{[1
]}

Endres, Kevin J. ^{[1
]}

Xie, Ting-Zheng ^{[1
]}

Wojtas, Lukasz ^{[3
]}

Moorefield, Charles N. ^{[4
]}

Wesdemiotis, Chrys ^{[1
,2
]}

Newkome, George R. ^{[1
,2
]}

机构：

[1] Univ Akron, Dept Polymer Sci, Akron, OH 44256 USA

[2] Univ Akron, Dept Chem, Akron, OH 44256 USA

[3] Univ S Florida, Dept Chem, 4202 East Fowler Ave, Tampa, FL 33620 USA

[4] Dendronex LLC, 109 Runway Dr, Lubbock, TX 79416 USA

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2017年 / 139卷 / 08期

基金：

美国国家科学基金会;

关键词：

METAL-ORGANIC FRAMEWORKS; SHAPE-PERSISTENT; ION MOBILITY; LIGAND; COMPLEXES; CONSTRUCTION; POLYMER; DESIGN; CONVERSION; NANOPRISMS;

D O I：

10.1021/jacs.6b11784

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A three-dimensional, highly symmetric sphere like nano cage was synthesized using a terpyridine (tpy)-based, flexible tris-dentate ligand and characterized by single crystal X-ray analysis. To introduce more rigidity, one of the tpy units of the tris-dentate ligand was preblocked by stable <tpy-Ru(2+)tpy> connectivity to form the corresponding Ru2+-dimer. The complexation between Ru2+-dimer and Fe2+ demonstrates an unexpected temperature-dependent assembly between two irreversible isomeric 3D nanocages. Investigation of the coordination process and structural configurations of the metal ligand framework, affected by the introduction of rigidity and in the presence of external stimuli (temperature), is reported.

引用

页码：3012 / 3020

页数：9

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