Examples of 'monochloride' in a sentence
Meaning of "monochloride"
monochloride (noun): A chemical compound containing one atom of chlorine for every atom of another element in the molecule
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- Any chloride containing a single chlorine atom in each molecule.
How to use "monochloride" in a sentence
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monochloride
Selenium monochloride was originally produced by the chlorination of selenium.
Precipitated triethylamine monochloride is removed by filtration.
Iodine monochloride is an interhalogen compound with the formula ICl.
Precipitated triethyamine monochloride is removed by filtration.
Catalyst preparation with and without using the monochloride.
Aluminium monochloride is the metal halide with the formula AlCl.
In certain embodiments the iodination reagent may be iodine monochloride.
Oxides have been reacted with sulfur monochloride and chlorine or sulfur monochloride alone.
Examples of interhalogen compounds are iodine monobromide and iodine monochloride.
Iodine is a solid at room temperature while iodine monochloride is a liquid at room temperature.
Suitable halogenating reagents include for example bromine and iodine monochloride.
The chlorinating agent is preferably a monochloride compound which only partially chlorinates the magnesium alkoxide.
Use of an alternative monochloride.
Then, sulfur monochloride is added into the polymer solution.
This compound is then iodinated by using one equivalent of iodine monochloride in alcohol.
See also
Diethyl aluminum monochloride and diisobutyl aluminum monochloride, a trialkyl aluminum e . g.
In another aspect, the catalyst is iodine monochloride.
Excess chlorine converts iodine monochloride into iodine trichloride in a reversible reaction,.
In particular, combinations of these cobalt compounds with a dialkyl aluminum monochloride e . g.
For the purposes of this invention, sulfur monochloride is considered equivalent to sulfur.
Xenon monochloride is used in excimer lasers . XeCl also exists in the excimer state.
It is advantageously chosen from diethylaluminium monochloride, ethylaluminium sesquichloride and diisobutylaluminium monochloride.
The invention can apply very advantageously to the production of chloro-cycloalkanes, in particular cyclohexyl monochloride.
Use according to claim 5, wherein said cyanuric monochloride is monosubstituted with a maleimide.
Treatment with chlorosulfonic acid gives the corresponding sulfonyl chloride, which is iodinated using iodine monochloride.
It may be chosen from diethylaluminium monochloride, ethylaluminium sesquichloride, diisobutylaluminium monochloride and ethoxydiethylaluminium.
Mention may be made, as preferred functionalization agent, of tributyltin monochloride or dibutyltin dichloride.
The iodine monochloride solution was added rapidly to the stirred solution of the 2 - ( methylamino ) benzoic acid.
Sulfurization of these esters is conducted with elemental sulfur, sulfur monochloride and / or sulfur dichloride.
Copper monochloride of a purity by weight of 96 % or more but not exceeding 99.
It may also be conducted with N - iodosuccinimide or iodine monochloride.
For the present invention, sulfur monochloride was purchased from Aldrich Co.
In another exemplary embodiment, the buffer is a mixture of L-histidine ( base ) and L-histidine monochloride monohydrate.
Copper monochloride of a purity by weight of 96 % or more but not more than 99.
Alternatively, in place of sulfur, sulfur monochloride may be employed.
At sulfur monochloride concentrations below 10 % v / w, this behavior is not visible in the swelling curves.
Twenty milliliters of a 0.5 molar solution of iodine monochloride in acetic acid is added.
Bromine monochloride ( BrCl ) is an unstable red-brown gas with a boiling point of 5 °C.
After bubbling nitrogen for 20 minutes, different amounts of sulfur monochloride are added under rigorous stirring.
For example, the protein fibrinogen is labeled with 125I using a twofold molar excess of iodine monochloride.
The reaction time is set to 3 days for sulfur monochloride concentrations less than 2.5 % v / w.
In tissues, 5 metabolites were identified, florfenicol, florfenicol-amine, florfenicol alcohol, florfenicol oxamid acid, monochloride florfenicol.
Reactions with 1, 1.5 and 2 equivalents of HCl afforded the same monochloride salt as a product.
The reduction is followed by iodination using 1-2 equivalents of iodine monochloride J. Org.
The buffer is a mixture of L-histidine ( base ) and L-histidine monochloride monohydrate.
