Heterotrimetallic Double Cavity Cages: Syntheses and Selective Guest Binding

被引:55
作者
Lisboa, Lynn S. [1 ]
Preston, Dan [2 ]
McAdam, C. John [1 ]
Wright, L. James [3 ]
Hartinger, Christian G. [3 ]
Crowley, James D. [1 ]
机构
[1] Univ Otago, Dept Chem, POB 56, Dunedin 9054, New Zealand
[2] Australian Natl Univ, Res Sch Chem, Canberra, ACT 0200, Australia
[3] Univ Auckland, Sch Chem Sci, Private Bag 92019, Auckland 1142, New Zealand
关键词
Double Cavity Cages; Heterometallic; Host-Guest Systems; Metallosupramolecular Architectures; Non-Cooperative Binding; COORDINATION; METALLACYCLES; DIMERIZATION; RECOGNITION; MULTICAVITY;
D O I
10.1002/anie.202201700
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A strategy for the generation of heterotrimetallic double cavity (DC) cages [PdnPtmL4](6+) (DC1: n=1, m=2; and DC2: n=2, m=1) is reported. The DC cages were generated by combining an inert platinum(II) tetrapyridylaldehyde complex with a suitably substituted pyridylamine and Pd-II ions. H-1 and DOSY nuclear magnetic resonance spectroscopy (NMR) and electrospray ionization mass spectrometry (ESIMS) data were consistent with the formation of the DC architectures. DC1 and DC2 were shown to interact with several different guest molecules. The structure of DC1, which features two identical cavities, binding two 2,6-diaminoanthraquinone (DAQ) guest molecules was determined by single-crystal X-ray crystallography. In addition, DC1 was shown to bind two molecules of 5-fluorouracil (5-FU) in a statistical (non-cooperative) manner. In contrast, DC2, which features two different cage cavities, was found to interact with two different guests, 5-FU and cisplatin, selectively.
引用
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页数:6
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