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Comparative study of CO insertion into pincer supported palladium alkyl and aryl complexes
The insertion of CO 2 into metal alkyl bonds is a crucial elementary step in transition metal-catalyzed processes for CO 2 utilization. Here, we synthesize pincer-supported palladium complexes of the type ( t Bu PBP)Pd(alkyl) ( t Bu PBP = B(NCH 2 P t Bu 2 ) 2 C 6 H 4 − ; alkyl = CH 2 CH 3 , CH 2 CH...
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Published in: | Chemical science (Cambridge) 2023-08, Vol.14 (3), p.8164-8179 |
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Main Authors: | , , , , |
Format: | Article |
Language: | |
Online Access: | Get full text |
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Summary: | The insertion of CO
2
into metal alkyl bonds is a crucial elementary step in transition metal-catalyzed processes for CO
2
utilization. Here, we synthesize pincer-supported palladium complexes of the type (
t
Bu
PBP)Pd(alkyl) (
t
Bu
PBP = B(NCH
2
P
t
Bu
2
)
2
C
6
H
4
−
; alkyl = CH
2
CH
3
, CH
2
CH
2
CH
3,
CH
2
C
6
H
5
, and CH
2
-4-OMe-C
6
H
4
) and (
t
Bu
PBP)Pd(C
6
H
5
) and compare the rates of CO
2
insertion into the palladium alkyl bonds to form metal carboxylate complexes. Although, the rate constant for CO
2
insertion into (
t
Bu
PBP)Pd(CH
2
CH
3
) is more than double the rate constant we previously measured for insertion into the palladium methyl complex (
t
Bu
PBP)Pd(CH
3
), insertion into (
t
Bu
PBP)Pd(CH
2
CH
2
CH
3
) occurs approximately one order of magnitude slower than (
t
Bu
PBP)Pd(CH
3
). CO
2
insertion into the benzyl complexes (
t
Bu
PBP)Pd(CH
2
C
6
H
5
) and (
t
Bu
PBP)Pd(CH
2
-4-OMe-C
6
H
4
) is significantly slower than any of the n-alkyl complexes, and CO
2
does not insert into the palladium phenyl bond of (
t
Bu
PBP)Pd(C
6
H
5
). While (
t
Bu
PBP)Pd(CH
2
CH
3
) and (
t
Bu
PBP)Pd(CH
2
CH
2
CH
3
) are resistant to β-hydride elimination, we were unable to synthesize complexes with
n
-butyl, iso-propyl, and
tert
-butyl ligands due to β-hydride elimination and an unusual reductive coupling, which involves the formation of new C-B bonds. This reductive process also occurred for (
t
Bu
PBP)Pd(CH
2
C
6
H
5
) at elevated temperature and a related process involving the formation of a new H-B bond prevented the isolation of (
t
Bu
PBP)PdH. DFT calculations provide insight into the relative rates of CO
2
insertion and indicate that steric factors are critical. Overall, this work is one of the first comparative studies of the rates of CO
2
insertion into different metal alkyl bonds and provides fundamental information that may be important for the development of new catalysts for CO
2
utilization.
The synthesis of a range of PBP supported palladium pincer complexes with different alkyl ligands is described. The rates of CO
2
insertion into the alkyl group are quantified and rationalized based on the identity of the alkyl ligand. |
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ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/d3sc01459b |