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Main group azido compounds are chemical compounds consisting of azide, N 3 − bonded to a main group element. [1] [2]Azido compounds are often shock sensitive.Their sensitivity correlates with the amount of ionic or covalent character the azide-element bond has, with ionic character being far more stable than covalent character. [3]
In chemistry, azide (/ ˈ eɪ z aɪ d /, AY-zyd) is a linear, polyatomic anion with the formula N − 3 and structure − N=N + =N −.It is the conjugate base of hydrazoic acid HN 3. Organic azides are organic compounds with the formula RN 3, containing the azide functional group. [1]
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[1] The cyclic form was identified in 2003 by N. Hansen and A. M. Wodtke using ultraviolet photolysis of chlorine azide. Although the reaction yielded mostly the linear form, about 20% of the molecules were cyclic. [4] [1] The ring has C 2v symmetry [1] —an isosceles triangle—in contrast to the linear form that has equal N–N bond-lengths.
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Methyl azide can be prepared by the methylation of sodium azide, for instance with dimethyl sulfate in alkaline solution, followed by passing through a tube of anhydrous calcium chloride or sodium hydroxide to remove contaminating hydrazoic acid. [1] The first synthesis was reported in 1905. [2] Decomposition to a nitrene is a first-order reaction:
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