Coordination of a Phosphine‐Tethered Aminoborane to Group 10 Metals

While π‐complexes of C=C bonds are ubiquitous in organometallic chemistry, analogous complexes of the isoelectronic but strongly polarized B=N double bond of aminoboranes are extremely scarce. To address this gap, a diphosphine‐aminoborane ligand (PhDPBAiPr) is introduced and its coordination with g...

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Vydané v:Chemistry : a European journal Ročník 30; číslo 32; s. e202400666 - n/a
Hlavní autori: Tiddens, Martine R., Kappé, Bram T., Smak, Tom J., Lutz, Martin, Moret, Marc‐Etienne
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Germany Wiley Subscription Services, Inc 06.06.2024
Predmet:
Acceptor ligands
aminoboranes
Bonding Analysis
Coordination
Crystal structure
Elongated structure
group 10 metals
Ligands
Magnetic resonance spectroscopy
Metals
NMR spectroscopy
Organometallic compounds
Palladium
Phosphine
Phosphines
π-ligands
Acceptor ligands
aminoboranes
group 10 metals
π-ligands
Bonding Analysis
ISSN:0947-6539, 1521-3765, 1521-3765
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Popis
Shrnutí:While π‐complexes of C=C bonds are ubiquitous in organometallic chemistry, analogous complexes of the isoelectronic but strongly polarized B=N double bond of aminoboranes are extremely scarce. To address this gap, a diphosphine‐aminoborane ligand (PhDPBAiPr) is introduced and its coordination with group 10 metals is investigated. The B=N bond does not coordinate to the metal in Pt(0) and Pd(II) complexes. In contrast, side‐on coordination of the B=N bond is observed in the Ni(0) complex (PhDPBAiPr)Ni(NCPh), and the X‐ray crystal structure reveals B−N bond elongation compared to the free ligand. The choice of co‐ligand strongly influences the presence or absence of side‐on coordination at Ni(0) as evidenced by NMR spectroscopy. While the B=N π‐complex is geometrically similar to C=C analogues, a bonding analysis reveals that the interaction of the B=N motif with the electron‐rich Ni(0) center is best described as 3c4e hyperbond, in which Ni and N are competing for the empty orbital on B. The synthesis and coordination chemistry of a diphosphine‐aminoborane ligand to group 10 metals is reported, affording a rare aminoborane π‐complex of Ni(0). The bonding situation is best described as a 3‐center‐4‐electron bond where the Ni and N atoms compete for an accepting orbital on boron. In contrast with isoelectronic olefin π‐complexes, the metal‐ligand bond is tenuous and the B=N ligand is therefore easily displaced.
Bibliografia:ObjectType-Article-1
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ISSN:0947-6539
1521-3765
1521-3765
DOI:10.1002/chem.202400666