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Single‐Site and Cooperative Bond Activation Reactions with Ylide‐Functionalized Tetrylenes: A Computational Study
Author(s) -
Steinert Henning,
Löffler Julian,
Gessner Viktoria H.
Publication year - 2021
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.202100816
Subject(s) - chemistry , ylide , protonation , main group element , catalysis , transition state , ligand (biochemistry) , boron , photochemistry , combinatorial chemistry , transition metal , stereochemistry , organic chemistry , ion , biochemistry , receptor
Due to their transition metal‐like behavior divalent group 14 compounds bear huge potential for their application in bond activation reactions and catalysis. Here we report on detailed computational studies on the use of ylide‐substituted tetrylenes in the activation of dihydrogen and phenol. A series of acyclic and cyclic ylidyltetrylenes featuring various α‐substituents with different σ ‐ and π ‐donating capabilities have been investigated which demonstrate that particularly π ‐accepting boryl groups lead to beneficial properties and low barriers for single‐site activation reactions, above all in the case of silylenes. In contrast, for the thermodynamically more stable germylenes and stannylenes an alternative mechanism involving the active participation of the ylide ligand in the E−H bond (E=H or PhO) activation process by addition across the element carbon linkage was found to be energetically favored. Furthermore, the boryl substituted tetrylenes allowed for a further activation pathway involving the active participation of the boron element bond. These cooperative mechanisms are especially attractive for the heavier cyclic ylidyltetrylenes in which the loss of the protonated ylide group is prevented due to the cyclic framework. Overall, the present studies suggest that cyclic ylide‐substituted germylenes and stannylenes bear huge potential for cooperative bond activations at mild conditions which should be experimentally addressed in the future.