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Far fewer such compounds are known than organoxenon compounds. The first organokrypton compound, HKrCCH, was reported in 2003 and made by photolytic insertion of a krypton atom into acetylene. Similar work was then done on diacetylene and cyanoacetylene, producing HKrC4H and HKrC3N. All these were made in matrix isolation and are stable up to 40 K. HKrCCF and HCCKrF have also been experimentally produced in matrix isolation.
Dications generated by dissociative electron ionisation of 2,4,6-trimethylpyridine react with krypton to form the organokrypton cations C8H7NKr and C8H8NKr. Reaction of acetylene dications with krypton produced HCCKr.
References
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