Dimorpholinoacetylene and Its Use for the Synthesis of Tetraaminocyclobutadiene Species

Koerner L, Luong Phong Ho , Puchta R, Stanger A, Tamm M (2022)


Publication Type: Journal article

Publication year: 2022

Journal

DOI: 10.1002/chem.202202737

Abstract

The new diaminoacetylene (DAA) dimorpholinoacetylene (3) was prepared from 1,1-dimorpholinoethene (1) by bromination to form the dibromoketene aminal 2, which upon lithiation afforded 3 through a Fritsch-Buttenberg-Wiechell rearrangement. Heating 3 at elevated temperatures resulted in a complete conversion into the dimer 1,1,2,4-tetramorpholino-1-buten-3-yne (4), which was used for the synthesis of four-membered cyclic bent allene (CBA) transition-metal complexes of the type [(CBA)MLn] (5-7; MLn=AuCl, RhCl(COD), RhCl(CO)2; CBA=1,3,4,4-tetramorpholino-1,2-cyclobutadiene; COD=1,5-cyclooctadiene). The reaction of 3 with tetraethylammonium bromide gave 1,2,3,4-tetramorpholinocyclobutenylium bromide (8), which reacted with bromine to form 1,2,3,4-tetra(morpholino)cyclobutenediylium bis(tribromide) (9). Compound 9 represents the first fully characterized compound containing a tetraaminocyclobutadiene dication and displays a nearly planar C4N4 core as shown by X-ray diffraction analysis. Detailed quantum chemical calculations were performed to assess the aromaticity of tetraaminocyclubutadiene dications by employing the Nucleus Independent Chemical Shift (NICS) method and current density analysis.

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APA:

Koerner, L., Luong Phong Ho, ., Puchta, R., Stanger, A., & Tamm, M. (2022). Dimorpholinoacetylene and Its Use for the Synthesis of Tetraaminocyclobutadiene Species. Chemistry - A European Journal. https://doi.org/10.1002/chem.202202737

MLA:

Koerner, Lukas, et al. "Dimorpholinoacetylene and Its Use for the Synthesis of Tetraaminocyclobutadiene Species." Chemistry - A European Journal (2022).

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