| Literature DB >> 29431286 |
André K Eckhardt1, Peter R Schreiner1.
Abstract
Although N-heterocyclic carbenes have been well-studied, the simplest aminocarbene, aminomethylene H-C̈-NH2 , has not been spectroscopically identified to date. Herein we report the gas-phase preparation of aminomethylene by high-vacuum flash pyrolysis of cyclopropylamine and subsequent trapping of the pyrolysate in an inert argon matrix at 12 K. Aminomethylene was characterized by matching matrix IR and UV/Vis spectroscopic data with ab initio coupled cluster computations. After UV irradiation of the matrix aminomethylene rearranges to its isomer methanimine (formaldimine) H2 C=NH. Based on our experimental results and computations aminomethylene has a singlet ground state with a reaction barrier of almost 46 kcal mol-1 to methanimine so that H-tunneling is excluded.Entities:
Keywords: amino acids; matrix isolation; origin of life; prebiotic chemistry; sugars
Year: 2018 PMID: 29431286 DOI: 10.1002/anie.201800679
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336