Cijanogen jehemijsko jedinjenje saformulom (CN)2. On je bezbojni, toksičnigas opornog zadaha. Ovaj molekul jepseudohalogen. Cijanogenski molekuli se sastoje od dve CN grupe - analogno diatomskim halogenim molekulima, kao što jeCl2, ali ima daleku manju oksidacionu sposobnost. Dvecijano grupe su vezane zajedno na njihovim atomimaugljenika: N≡C−C≡N, mada su i drugi izomeri poznati.[7] Pojedini derivati cijanogena se takođe nazivaju "cijanogen" čak i kad sadrže samo jednu CN grupu. Na primercijanogen bromid ima formulu NCBr.[8]
↑1,01,1„oxalonitrile (CHEBI:29308)”. Chemical Entities of Biological Interest. UK: European Bioinformatics Institute. 27. 10. 2006.. Main. Pristupljeno 6. 6. 2012.
↑2,02,12,2NIOSH Pocket Guide to Chemical Hazards. Department of Health and Human Services, Centers for Disease Control, National Institute for Occupational Safety & Health. September 2007. str. 82.
↑3,03,1The Merck Index (10th izd.). Rahway, NJ: Merck & Co.. 1983. str. 385.
↑Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑Ringer, A. L.; Sherrill, C. D.; King, R. A.; Crawford, T. D. (2008). „Low-lying singlet excited states of isocyanogen”. International Journal of Quantum Chemistry106 (6): 1137–1140. Bibcode2008IJQC..108.1137R. DOI:10.1002/qua.21586.
↑Hartman, W. W.; Dreger, E. E. (1931), „Cyanogen Bromide”, Organic Syntheses11: 30;Coll. Vol.2: 150
↑Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd izd.). Oxford: Butterworth-Heinemann. str. 320-321. ISBN0080379419.
NIOSH Pocket Guide to Chemical Hazards. Department of Health and Human Services, Centers for Disease Control, National Institute for Occupational Safety & Health. September 2007. str. 82.
The Merck Index (10th izd.). Rahway, NJ: Merck & Co.. 1983. str. 385.
Y
F+
T
N
