| Literature DB >> 29711483 |
Daniel J Mindiola1, Christopher C Cummins1.
Abstract
Instead of azides, which can be explosive and poorly soluble in nonpolar solvents, azabicycloheptadienes can be used to synthesize nitrides. The reaction of diiodide 1 with the lithium amide 3 provides the red nitride 2 in 60 % yield with loss of lithium iodide and anthracene. The remaining iodo ligand in 2 can undergo an exchange reaction with lithium amide 3, but no more anthracene is released. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.Entities:
Keywords: Azides; Chromium; N ligands; Nitrides; Nitrogen
Year: 1998 PMID: 29711483 DOI: 10.1002/(SICI)1521-3773(19980420)37:7<945::AID-ANIE945>3.0.CO;2-X
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336