2,2'-Dipyridylamine

2,2′-Dipyridylamine Dipyridylamine.png N-(Pyridin-2-yl)pyridin-2-amine 2,2′-Iminodipyridine 1202-34-2 14547 13888 1735909 214-864-3 X9BF664YAK DTXSID5061619 1S/C10H9N3/c1-3-7-11-9(5-1)13-10-6-2-4-8-12-10/h1-8H,(H,11,12,13) HMMPCBAWTWYFLR-UHFFFAOYSA-N C1=CC=NC(=C1)NC2=CC=CC=N2 10 9 3 white solid 90.5 307.5 07 Warning 315 319 335 261 264 271 280 302+352 304+340 305+351+338 312 321 332+313 337+313 362 403+233 405 501 2,2′-Dipyridylamine is an organic compound with the formula (C5H4N)2NH. It consists of a pair of 2-pyridyl groups (C5H4N) linked to a secondary amine. The compound forms a range of coordination complexes.10.1016/S0010-8545(00)00403-3 Luminescence and electroluminescence of Al(III), B(III), Be(II) and Zn(II) complexes with nitrogen donors 2001 Wang Suning Coordination Chemistry Reviews 215 79–98 Its conjugate base, 2,2′-dipyridylamide, forms extended metal atom chains.10.1021/JA971997H Symmetrical and Unsymmetrical Compounds Having a Linear Co36+ Chain Ligated by a Spiral Set of Dipyridyl Anions 1997 Cotton F. Albert Daniels Lee M. Jordan Murillo Carlos A. Journal of the American Chemical Society 119 43 10377–10381 Formation 2,2′-Dipyridylamine can be formed by heating pyridine with sodium amide. Alternatively, 2-aminopyridine can be heated with 2-chloropyridine over barium oxide.Brogden David W. Berry John F. Coordination Chemistry of 2,2′-Dipyridylamine: The Gift That Keeps on Giving Comments on Inorganic Chemistry 4 September 2015 36 1 17–37 10.1080/02603594.2015.1079522 101638568 References Category:2-Pyridyl compounds Category:Chelating agents