1,4-Phosphagermines: An Anionic 6π-heteroaromatic Biradicaloid and a Persistent π-Delocalized Radical

Dihetarenes with identical third-period or heavier elements are well established, whereas mixed-element analogues are not. Here, we report the synthesis and characterization of a 1,4-phosphagermine anion and its persistent delocalized radical. The unique synthetic protocol presented herein should be adaptable to other combinations of mixed-heavy main-group elements. Computational analyses (2D-XY NICS<sub>π,zz</sub><sup>SOM</sup> scans and ELF<sub>π</sub>) identify it as an aromatic P,Ge-heterocycle, which nonetheless possesses significant biradicaloid character as revealed by PW6B95-D3BJ/def2-QZVP(CPCM<sub>THF</sub>)//TPSS-D3BJ/def2-TZVP(CPCM<sub>THF</sub>) and CASSCF (CASSCF(X,Y)/NEVPT2/def2-TZVP) calculations. Electrochemical studies demonstrate the stability of the radical species, while mild chemical oxidation of the aromatic anion produces the radical, which was identified in solution by EPR spectroscopy. These findings expand the frontier of main-group chemistry, highlighting the potential of mixed-heavy-element aromatic systems. A detailed, comprehensive theoretical study (PW6B95-D3BJ/def2-TZVP(CPCM<sub>THF</sub>) level of theory) on 16 combinations of heavy group 14/15 elements reveals an increasing tendency for a biradicaloid character but not the alternative Dewar structure.

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Journal
Inorganic Chemistry
Published
2025-06-18
DOI
https://doi.org/10.1021/acs.inorgchem.5c01531
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

1,4-Phosphagermines: An Anionic 6π-heteroaromatic Biradicaloid and a Persistent π-Delocalized Radical

Tatjana Terschüren, Rosa M. Gomila, Olav Schiemann, Antonio Frontera et al.
4 links
Inorganic Chemistry
Organoboron and organosilicon chemistry
article

1,4-Phosphagermines: An Anionic 6π-heteroaromatic Biradicaloid and a Persistent π-Delocalized Radical

Tatjana Terschüren, Rosa M. Gomila, Olav Schiemann, Antonio Frontera, Gregor Schnakenburg, Philipp C. Brehm, Surendar Karwasara, Mridhul R. K. Ramachandran, Rainer Streubel, Renè T. Boeré, Takahiro Sasamori
article en

Abstract

Dihetarenes with identical third-period or heavier elements are well established, whereas mixed-element analogues are not. Here, we report the synthesis and characterization of a 1,4-phosphagermine anion and its persistent delocalized radical. The unique synthetic protocol presented herein should be adaptable to other combinations of mixed-heavy main-group elements. Computational analyses (2D-XY NICS<sub>π,zz</sub><sup>SOM</sup> scans and ELF<sub>π</sub>) identify it as an aromatic P,Ge-heterocycle, which nonetheless possesses significant biradicaloid character as revealed by PW6B95-D3BJ/def2-QZVP(CPCM<sub>THF</sub>)//TPSS-D3BJ/def2-TZVP(CPCM<sub>THF</sub>) and CASSCF (CASSCF(X,Y)/NEVPT2/def2-TZVP) calculations. Electrochemical studies demonstrate the stability of the radical species, while mild chemical oxidation of the aromatic anion produces the radical, which was identified in solution by EPR spectroscopy. These findings expand the frontier of main-group chemistry, highlighting the potential of mixed-heavy-element aromatic systems. A detailed, comprehensive theoretical study (PW6B95-D3BJ/def2-TZVP(CPCM<sub>THF</sub>) level of theory) on 16 combinations of heavy group 14/15 elements reveals an increasing tendency for a biradicaloid character but not the alternative Dewar structure.

Inorganic ChemistryVol. 64(26)
University of Lethbridge (CA), University of Bonn (DE), University of Tsukuba (JP), Universitat de les Illes Balears (ES)
Alexander von Humboldt-Stiftung, University of Lethbridge, Ministerio de Ciencia, Innovación y Universidades, Natural Sciences and Engineering Research Council of Canada, European Regional Development Fund
Openalex Percentile: Top 89%
Organoboron and organosilicon chemistry
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