AC Kolloquium - Dr. habil. Christian Hering-Junghans
Non-Classical Double Bonds – Phoshaalkenes and Phosphaalumenes
Heavier element–element multiple bonds had been long considered inaccessible but have now moved beyond the status of lab curiosities. However, heteroatomic E13═E15 (E13 = Al, Ga; E15 = N, P, As) multiple bonds are still scarcely represented. Due to alternating Lewis acidic and Lewis basic centers, E13=E15 species are prone to oligomerize. Oligomerization can be suppressed by either kinetic, acceptor or donor stabilization. In our quest to design novel phosphaalkene-based ligand systems through the so-called phospha-Wittig reaction, we have uncovered the potential of phospha-Wittig reagents (ArPPMe3) as phosphinidene transfer reagents. These species allow facile access to phosphaalumenes and -gallenes in the reaction with sources of Al(I) opr Ga(I), respectively.
Heavier element–element multiple bonds had been long considered inaccessible but have now moved beyond the status of lab curiosities. However, heteroatomic E13═E15 (E13 = Al, Ga; E15 = N, P, As) multiple bonds are still scarcely represented. Due to alternating Lewis acidic and Lewis basic centers, E13=E15 species are prone to oligomerize. Oligomerization can be suppressed by either kinetic, acceptor or donor stabilization. In our quest to design novel phosphaalkene-based ligand systems through the so-called phospha-Wittig reaction, we have uncovered the potential of phospha-Wittig reagents (ArPPMe3) as phosphinidene transfer reagents. These species allow facile access to phosphaalumenes and -gallenes in the reaction with sources of Al(I) opr Ga(I), respectively.
Zeit
Donnerstag, 24.10.24 - 14:00 Uhr
- 15:30 Uhr
Themengebiet
Chemie
Referierende
Dr. habil. Christian Hering-Junghans - Leibniz Institute for Catalysis
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Ort
Bonn
Raum
Hörsaal 1
Reservierung
nicht erforderlich
Veranstalter
Institut für Anorganische Chemie
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