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Reversible uptake of CO2 by pincer ligand supported dimetallynes

Abstract:
We report on the reversible uptake of carbon dioxide by dimetallynes featuring ancillary hemi‐labile pincer ligands. Insertion into the Ge−Ge/Sn−Sn bonds yields species containing an E(CO2)E unit, with the mode of ligation of the CO2 fragment determined crystallographically being found to be dependent on the identity of the Group 14 element. The thermodynamics of CO2 uptake/loss can be established through VT NMR (ΔH°=+24.6(2.3) kJ mol−1, ΔS°=+64.9(3.8) J mol−1 K−1, ΔG°298=+5.3(1.9) kJ mol−1 for the loss of CO2 in the Ge case), and the chemical consequences of reversibility demonstrated by thermodynamically‐controlled exchange reactions.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/ange.202117496

Authors

More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Oxford college:
Queen's College
Role:
Author
ORCID:
0000-0001-9998-9434


Publisher:
Wiley
Journal:
Angewandte Chemie More from this journal
Volume:
134
Issue:
17
Article number:
e202117496
Publication date:
2022-02-26
Acceptance date:
2022-02-10
DOI:
EISSN:
1521-3757
ISSN:
0044-8249


Language:
English
Keywords:
Pubs id:
1790429
Local pid:
pubs:1790429
Source identifiers:
W4211045340
Deposit date:
2026-11-06
ARK identifier:

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