dc.contributor.author |
Ghana, Priyabrata |
|
dc.contributor.author |
Morris, Louis J. |
|
dc.contributor.author |
Okuda, Jun |
|
dc.coverage.spatial |
United Kingdom |
|
dc.date.accessioned |
2025-06-12T06:23:41Z |
|
dc.date.available |
2025-06-12T06:23:41Z |
|
dc.date.issued |
2025-05 |
|
dc.identifier.citation |
Ghana, Priyabrata; Morris, Louis J. and Okuda, Jun, "Reactive main group metal complexes of the neutral NNNN macrocycle, Me4TACD", Dalton Transactions, DOI: 10.1039/D4DT03357D, May 2025. |
|
dc.identifier.issn |
1477-9226 |
|
dc.identifier.issn |
1477-9234 |
|
dc.identifier.uri |
https://doi.org/10.1039/D4DT03357D |
|
dc.identifier.uri |
https://repository.iitgn.ac.in/handle/123456789/11515 |
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dc.description.abstract |
Currently, there is considerable interest in introducing molecularly defined main group metal compounds as precursors and model complexes of homogeneous catalysts for various bond cleavage and forming transformations. With a focus on the NNNN macrocyclic ligand Me4TACD (N,N′,N′′,N′′′-tetramethyl-1,4,7,10-tetraazacyclododecane), this review summarizes the versatility of the ligand Me4TACD for the stabilization of reactive main group s- and p-block (group 1, 2, 12–14) metals. Metal hydrides, hydrocarbyls and silyls are often monomeric and catalyze alkene hydrofunctionalisations. In contrast to the rich coordination chemistry of d- and f-block transition metals using a plethora of ligands, main group metals still leave room for new structures and reactivities, aligning with the current efforts to develop a systematic understanding in s- and p-block metal–ligand combinations. |
|
dc.description.statementofresponsibility |
by Priyabrata Ghana, Louis J. Morris and Jun Okuda |
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dc.language.iso |
en_US |
|
dc.publisher |
Royal Society of Chemistry |
|
dc.title |
Reactive main group metal complexes of the neutral NNNN macrocycle, Me4TACD |
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dc.type |
Article |
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dc.relation.journal |
Dalton Transactions |
|