Phenoxy-imino ligands: coordination chemistry and binding properties with copper(II) cations

Author(s):  
Kelvin Wambugu ◽  
George S. Nyamato ◽  
Joanne Ogunah ◽  
Stephen O. Ojwach
2012 ◽  
Vol 65 (2) ◽  
pp. 298-307 ◽  
Author(s):  
Stephen O. Ojwach ◽  
George S. Nyamato ◽  
Benard Omondi ◽  
James Darkwa ◽  
Alexander O. Okoth

2012 ◽  
Vol 392 ◽  
pp. 141-147 ◽  
Author(s):  
Stephen O. Ojwach ◽  
George S. Nyamato ◽  
Benard Omondi ◽  
James Darkwa

2001 ◽  
Vol 73 (7) ◽  
pp. 1041-1057 ◽  
Author(s):  
Jonathan L. Sessler ◽  
Rebecca S. Zimmerman ◽  
Christophe Bucher ◽  
Vladimír Král ◽  
Bruno Andrioletti

Calixphyrins are a class of hybrid molecules that lie at the structural crossroads between porphyrins and calixpyrroles. Porphyrins, long known for their versatile metal cation coordination chemistry, are macrocycles that contain only sp2-hybridized bridging meso carbon atoms within their framework. Calix[n]pyrroles, on the other hand, are porphyrin analogs that contain pyrroles bridged exclusively by sp3 meso carbon centers, and in recent years have been shown to display remarkable anion-binding properties. Calix[n]phyrins bear analogy to both the porphyrins and calixpyrroles and are macrocyclic analogs that contain a mixture of sp2- and sp3-hybridized meso carbon bridges. This leads to partial interruptions in the conjugation pathway of the molecule, introduces novel structural features, and leads to interesting anion and cation recognition properties. It also allows for modular syntheses. In the present paper, the chemistry of calix[n]phyrins, still at an early stage of exploration, is reviewed.


Author(s):  
Martin Poenie ◽  
Akwasi Minta ◽  
Charles Vorndran

The use of fura-2 as an intracellular calcium indicator is complicated by problems of rapid dye leakage and intracellular compartmentalization which is due to a probenecid sensitive anion transporter. In addition there is increasing evidence for localized microdomains of high calcium signals which may not be faithfully reported by fura-2.We have developed a new family of fura-2 analogs aimed at addressing some of these problems. These new indicators are based on a modified bapta which can be readily derivatized to produce fura-2 analogs with a variety of new properties. The modifications do not affect the chromophore and have little impact on the spectral and metal binding properties of the indicator. One of these new derivatives known as FPE3 is a zwitterionic analog of fura-2 that can be loaded into cells as an acetoxymethyl ester and whose retention in cells is much improved. The improved retention of FPE3 is important for both cuvettebased measurements of cell suspensions and for calcium imaging.


1998 ◽  
Vol 36 (5) ◽  
pp. 291-298 ◽  
Author(s):  
DE LUCCA ◽  
BLAND ◽  
JACKS ◽  
GRIMM ◽  
WALSH

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