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1.
J Am Chem Soc ; 125(34): 10186-7, 2003 Aug 27.
Article in English | MEDLINE | ID: mdl-12926937

ABSTRACT

A long-standing problem in cucurbituril chemistry is answered through the first direct functionalization of cucurbit[n]uril (CB[n]; n = 5-8)) leading to perhydroxyCB[n] which can be further modified to provide tailored CB[n] derivatives with desired functional groups and good solubility. Anchoring a CB[6] derivative on the surface and its potential application as a sensor are demonstrated. A CB[6] derivative forms nanospheres with possible use in protein and peptide drug delivery.

3.
J Am Chem Soc ; 124(19): 5374-9, 2002 May 15.
Article in English | MEDLINE | ID: mdl-11996578

ABSTRACT

Ion selective electrodes (ISE) based on three different tripodal receptors (5, 6, and 7) have been investigated for sensing ammonium ion. Each receptor is based on three pyrazole groups that can accept three H-bonds from the bound ammonium ion. The receptor based on 4-bromo-3,5-dimethylpyrazole (6) is the most sensitive with a detection limit for ammonium ion of 2.5 x 10(-5) M at pH 8. The detection limits for the receptors based on 2,3-dimethylpyrazole (5) and unsubstitued pyrazole (7) are 1.0 x 10(-4) and 2.0 x 10(-4) M, respectively. The selectivities of the receptors 5, 6, and 7 for sensing ammonium ion over potassium ion (logK(NH)4+(/K)+) are -2.8, -2.3, and -1.7, respectively. In contrast, the detection limit and the selectivity of a nonactin-based ISE are 2.2 x 10(-5) M and -1.3, respectively. Crystallographic studies reveal that 6 accepts three H-bonds from the bound ammonium and singly protonated receptor 5 forms three H-bonds with the bound water molecule.


Subject(s)
Anti-Bacterial Agents/chemistry , Macrolides/chemistry , Pyrazoles/chemistry , Quaternary Ammonium Compounds/chemistry , Receptors, Drug/chemistry , Crystallography, X-Ray , Electrodes , Hydrogen-Ion Concentration , Kinetics , Molecular Structure , Stereoisomerism
5.
Angew Chem Int Ed Engl ; 40(11): 2116-2119, 2001 Jun 01.
Article in English | MEDLINE | ID: mdl-29712191

ABSTRACT

A cage-type receptor binds an NH4+ ion by cation-π interactions and hydrogen bonding with high sensitivity and selectivity, comparable or even superior to those of the natural antibiotic nonactin over a wide pH range. The high performance, low cost, and easy synthesis may offer practical applications for this receptor as an ammonium ion sensor.

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