imidazole

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imidazole

 [im″id-az´ōl]
1. an organic compound in which two of the five atoms that make up the ring are nitrogen atoms. It is an antimetabolite and inhibitor of histamine and is used as an insecticide.
2. any of a class of antifungal agents that contain this compound.

im·id·a·zole

(im-id'ă-zōl),
A five-membered heterocyclic compound occurring in l-histidine and other biologically important compounds.

imidazole

(ĭm′ĭ-dăz′ōl′)
n.
1. An organic crystalline base, C3H4N2, that is an inhibitor of histamine.
2. Any of various derivatives of this compound, which often have antifungal, anthelmintic, or antibiotic properties.

im·id·a·zole

(i-mid'i-zōl)
A five-membered heterocyclic compound occurring in l-histidine and other biologically important compounds.
References in periodicals archive ?
The preparation of montmorillonite/PS nanocomposites by the use of two new thermally stable imidazolium surfactants ([C.sub.20] and [C.sub.22]) showed that it is possible to increase the exfoliation degree by increasing the length of the alkyl chain present in thermally stable surfactant structure.
In the part B and C, the peaks at 3110 [cm.sup.-1] and 1580 [cm.sup.-1] belonged to -CH stretching and bending vibration of imidazolium cation [18].
This may be due to that the imidazolium is acting as an unstable base cation [32].
Investigation of interaction kinetics of ED-20 and PDI-3AK epoxy oligomers with IMTHPA curing agent in the presence of 1-butyl-3-methyl imidazolium salts by using DSC method has shown these oligomers to be catalysts of polyaddition reaction.
It was interesting to notice that on changing the cation from imidazolium ([Emim][I]) to pyridinium ([Epyr][I]), quite different phase behavior was observed.
Synthesis of 1-(4-vinylbenzyl)-3-Butyl Imidazolium Tetrafluoroborate (VBIT)
Scott, "1-methylimidazole stabilization of gold nanoparticles in imidazolium ionic liquids," Chemical Communications, no.
When the hydrogen of C(2) of imidazolium ring was replaced by methyl, it lowered the hydrogen bond of cation and anion of ILs; the anion of ILs functions with the hydrogen of thionucleobase was stronger, which accelerate the thiosubstituted reactions.
The electrolyte consisted of 0.6 M N-methyl-N-butyl imidazolium iodide (BMII) + 0.1 M LiI + 0.05 M I2 + 0.5 M 4-tert-butyl pyridine (TBP) in acetonitrile.
The exception may result from the incompatibility between P(MVT-VT) and imidazolium of [H.sub.3][PO.sub.4] and Imi.