Coinage metal aluminyl complexes: probing regiochemistry and mechanism in the insertion and reduction of carbon dioxide

The synthesis of coinage metal aluminyl complexes, featuring M-Al covalent bonds, is reported via a salt metathesis approach employing an anionic Al( i ) ('aluminyl') nucleophile and group 11 electrophiles. This approach allows access to both bimetallic (1 : 1) systems of the type ( t Bu 3...

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Bibliographic Details
Published in:Chemical science (Cambridge) 2021-10, Vol.12 (4), p.13458-13468
Main Authors: McManus, Caitilín, Hicks, Jamie, Cui, Xianlu, Zhao, Lili, Frenking, Gernot, Goicoechea, Jose M, Aldridge, Simon
Format: Article
Language:English
Subjects:
Aluminum
Bimetals
Carbodiimides
Carbon dioxide
Chemical bonds
Chemistry
Coordination compounds
Copper
Covalent bonds
Crystallography
Extrusion rate
Gold
Insertion
Low temperature
Metathesis
Nucleophiles
Quantum chemistry
Silver
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Summary:The synthesis of coinage metal aluminyl complexes, featuring M-Al covalent bonds, is reported via a salt metathesis approach employing an anionic Al( i ) ('aluminyl') nucleophile and group 11 electrophiles. This approach allows access to both bimetallic (1 : 1) systems of the type ( t Bu 3 P)MAl(NON) (M = Cu, Ag, Au; NON = 4,5-bis(2,6-diisopropylanilido)-2,7-di- tert -butyl-9,9-dimethylxanthene) and a 2 : 1 di(aluminyl)cuprate system, K[Cu{Al(NON)} 2 ]. The bimetallic complexes readily insert heteroallenes (CO 2 , carbodiimides) into the unsupported M-Al bonds to give systems containing a M(CE 2 )Al bridging unit (E = O, NR), with the μ-κ 1 (C):κ 2 (E,E′) mode of heteroallene binding being demonstrated crystallographically for carbodiimide insertion in the cases of all three metals, Cu, Ag and Au. The regiochemistry of these processes, leading to the formation of M-C bonds, is rationalized computationally, and is consistent with addition of CO 2 across the M-Al covalent bond with the group 11 metal acting as the nucleophilic partner and Al as the electrophile. While the products of carbodiimide insertion are stable to further reaction, their CO 2 analogues have the potential to react further, depending on the identity of the group 11 metal. ( t Bu 3 P)Au(CO) 2 Al(NON) is inert to further reaction, but its silver counterpart reacts slowly with CO 2 to give the corresponding carbonate complex (and CO), and the copper system proceeds rapidly to the carbonate even at low temperatures. Experimental and quantum chemical investigations of the mechanism of the CO 2 to CO/carbonate transformation are consistent with rate-determining extrusion of CO from the initially-formed M(CO) 2 Al fragment to give a bimetallic oxide that rapidly assimilates a second molecule of CO 2 . The calculated energetic barriers for the most feasible CO extrusion step (Δ G ‡ = 26.6, 33.1, 44.5 kcal mol −1 for M = Cu, Ag and Au, respectively) are consistent not only with the observed experimental labilities of the respective M(CO) 2 Al motifs, but also with the opposing trends in M-C (increasing) and M-O bond strengths (decreasing) on transitioning from Cu to Au. The differential reactivity of copper, silver and gold aluminyl compounds towards CO 2 and other heteroallenes are probed by experimental and quantum chemical methods.
ISSN:2041-6520
2041-6539
DOI:10.1039/d1sc04676d