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SUMMARY:AC Kolloquium -  Prof. Dr. Simon Aldridge
DTSTART;TZID=Europe/Berlin:20260211T160000
DTEND;TZID=Europe/Berlin:20260211T170000
DTSTAMP:20260426T053348Z
UID:e928bac9a435484aa921f9c73dc234b8@www.chemie.uni-bonn.de
CATEGORIES:ac-events,Lu-events
CREATED:20260126T113252Z
DESCRIPTION:Unleashing New Patterns of Reactivity with Electron-Rich Main 
 Group Compounds\n\nThe development of main group compounds for small molec
 ule activation\, traditionally the domain of transition metals\, is a rapi
 dly growing area. p-Block systems can activate diverse substrates and are 
 increasingly applied in heavy-metal-free catalysis. Our research targets g
 roup 13 and 14 metals with frontier orbitals suited for cooperative activa
 tion of H₂\, NH₃\, and CO\, with reactivity tuned via HOMO–LUMO ener
 gies. Aluminyl systems (AlX₂⁻) show unusual reactivity due to high nuc
 leophilicity\, including arene C–H activation\, CO homologation\, and un
 precedented benzene C–C bond cleavage. Their electron-rich nature also e
 nables use as metallo-ligands in bimetallic compounds. Recent Be(I) specie
 s act as strong σ-donor ligands\, opening access to novel valence states 
 and reactivity in d-block metals.
LAST-MODIFIED:20260126T120529Z
URL:https://www.chemie.uni-bonn.de/lu/de/lu-events/ac-kolloquium-prof-dr-s
 imon-aldridge
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TZID:Europe/Berlin
X-LIC-LOCATION:Europe/Berlin
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DTSTART:20251026T020000
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TZOFFSETFROM:+0200
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