Crystal structure of ((S)-malato)tetraaquamagnesium(II) hydrate. Versatility of (S)-malate-metal ion binding

1979 ◽  
Vol 18 (11) ◽  
pp. 3034-3037 ◽  
Author(s):  
Anastas Karipides
1989 ◽  
Vol 122 (8) ◽  
pp. 1445-1447 ◽  
Author(s):  
Hubert Schmidbaur ◽  
Ina Bach ◽  
Dallas L. Wilkinson ◽  
Gerhard Müller

Biochemistry ◽  
1994 ◽  
Vol 33 (20) ◽  
pp. 6295-6300 ◽  
Author(s):  
Erli Zhang ◽  
Marcos Hatada ◽  
John M. Brewer ◽  
Lukasz Lebioda

1977 ◽  
Vol 16 (12) ◽  
pp. 3299-3302 ◽  
Author(s):  
Anastas. Karipides ◽  
James. Ault ◽  
A. Thomas. Reed

RSC Advances ◽  
2017 ◽  
Vol 7 (74) ◽  
pp. 46980-46988 ◽  
Author(s):  
Dongqin Bi ◽  
Yuquan Feng ◽  
Qian Zhao ◽  
Hongwei Wang ◽  
Yongsheng Zhu ◽  
...  

The “Donor–Phosphore–Receptor” platform as a novel building block for formation of heterotrinuclear transition metal complexes.


2004 ◽  
Vol 69 (4) ◽  
pp. 885-896 ◽  
Author(s):  
Luisa Stella Dolci ◽  
Péter Huszthy ◽  
Erika Samu ◽  
Marco Montalti ◽  
Luca Prodi ◽  
...  

Enantiomerically pure dimethyl- and diisobutyl-substituted phenazino-18-crown-6 ligands bind metal and ammonium ions and also primary aralkylammonium perchlorates in acetonitrile with high affinity, causing pronounced changes in their luminescence properties. In addition, they show enantioselectivity towards chiral primary aralkylammonium perchlorates. The possibility to monitor the binding process by photoluminescence spectroscopy can gain ground for the design of very efficient enantioselective chemosensors for chiral species. The observed changes in the photophysical properties are also an important tool for understanding the interactions present in the adduct.


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