A versatile nitrogen ligand for alkaline-earth chemistry
Author(s) -
Peter M. Chapple,
Marie Cordier≈,
Vincent Dorcet,
Thierry Roisnel,
JeanFrançois Carpentier,
Yann Sarazin
Publication year - 2020
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/d0dt02236e
Subject(s) - alkaline earth metal , ligand (biochemistry) , chemistry , inorganic chemistry , nitrogen , combinatorial chemistry , alkali metal , organic chemistry , receptor , biochemistry
The tridentate ligand 1,8-bis-(2,6-diisopropylphenyl)imino-3,6-di-tert-butyl-carbazolate, {Carb DiPP } - , has been used to prepare a variety of complexes of the large alkaline earths (Ae) calcium, strontium and barium. A complex of their smaller congener, magnesium, has also been synthesised. The range of coligands that have been utilised include alkyls, amides, halides and tetrelides. All structurally characterised complexes presented herein are stable in solution and do not undergo ligand redistribution that is otherwise well-known to pollute the chemistry of the alkaline-earth metals. Detailed structural and spectroscopic data for these compounds are discussed. They provide compelling evidence that this nitrogen ligand allows for the kinetic stabilisation of Ae complexes through optimal steric encapsulation of the voluminous metal centres. Its ease of access combined to its evident versatility make {Carb DiPP }H stand out in the portfolio of proligands that have been devised for similar purposes in the past decade. Yet, it fell short in our attempts to synthesise heteroleptic Ae-hydrides upon action of PhSiH 3 onto Ae-amides, as the crystallised products showed the imine groups were prone to hydride reduction and formal hydrosilylation.
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