Synthesis and Properties of Metal-Ligand Complexes with Endohedral Amine Functionality

被引:58
作者
Johnson, Amber M. [1 ]
Moshe, Orly [1 ]
Gamboa, Ana S. [1 ]
Langloss, Brian W. [1 ]
Limtiaco, John F. K. [1 ]
Larive, Cynthia K. [1 ]
Hooley, Richard J. [1 ]
机构
[1] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
基金
美国国家科学基金会;
关键词
MOLECULAR RECOGNITION; SUPRAMOLECULAR CATALYSIS; TRIGONAL PRISMS; HOST; CAGE; STABILIZATION; NMR; PALLADIUM(II); CHEMISTRY; DISCRETE;
D O I
10.1021/ic201092s
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of tetracationic M2L4 palladium-pyridyl complexes with endohedral amine functionality have been synthesized. The complexes were analyzed by NMR techniques (including Diffusion NMR and 2D NOESY), electrospray ionization (ESI) mass spectrometry, and X-ray crystallography. The solid state analysis shows a large change in crystal morphology upon introduction of the endohedral amine groups, caused by deleterious interactions between the amines and the triflate counterions from the coordination process. Combination of different ligands allows analysis of ligand exchange rates via NMR analysis, with half-lives on the order of 3 h, independent of the donor properties of the ligand. Self-sorting behavior is observed, with more electron-rich ligands being favored. The amine-containing and extended complexes are strongly fluorescent, giving quantum yields of up to 83%.
引用
收藏
页码:9430 / 9442
页数:13
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