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Cyanogen
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==Reactions== For the two less stable isomers of cyanogen, the order of the atoms differs. Isocyanogen (or cyanogen cyanide) is {{chem2|-C\tN+\sC\tN}}.<ref>{{cite journal |doi=10.1021/j100191a027 |title=Central Bond in the Three CN.cntdot.dimers NC-CN, CN-CN and CN-NC: Electron Pair Bonding and Pauli Repulsion Effects |date=1992 |last1=Bickelhaupt |first1=F. Matthias |last2=Nibbering |first2=Nico M. M. |last3=Van Wezenbeek |first3=Egbert M. |last4=Baerends |first4=Evert Jan |journal=The Journal of Physical Chemistry |volume=96 |issue=12 |pages=4864–4873}}</ref> It has been detected in the [[interstellar medium]].<ref>{{cite journal |doi=10.3847/2041-8213/aad089|doi-access=free |title=Discovery of Interstellar Isocyanogen (CNCN): Further Evidence that Dicyanopolyynes Are Abundant in Space |date=2018 |last1=Agúndez |first1=M. |last2=Marcelino |first2=N. |last3=Cernicharo |first3=J. |journal=The Astrophysical Journal Letters |volume=861 |issue=2 |pages=L22 |pmid=30186588 |pmc=6120679 |arxiv=1806.10328 |bibcode=2018ApJ...861L..22A}}</ref> Addition of [[disulfur dichloride]] to cyanogen gives [[3,4-Dichloro-1,2,5-thiadiazole|3,4-dichloro-1,2,5-thiadiazole]].
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