Journal article
Triaminoborane-bridged diphosphine complexes with Ni and Pd: coordination chemistry, structures, and ligand-centered reactivity
Dalton transactions : an international journal of inorganic chemistry, Vol.46(29), pp.9394-9406
07/25/2017
DOI: 10.1039/c7dt02144e
PMID: 28695953
Abstract
The synthesis, coordination chemistry, and reactivity of two diphosphines containing the cyclic triaminoborane 1,8,10,9-triazaboradecalin (TBD) are described. To evaluate the ligand-centered reactivity of
TBDPhos and
TBDPhos, the complexes (
TBDPhos)MCl
and (
TBDPhos)MCl
, where M = Ni and Pd, were prepared and characterized by elemental analysis, multinuclear NMR spectroscopy (
H,
C,
P, and
B), and single-crystal X-ray diffraction (XRD). Despite very low boron Lewis acidity in the TBD backbone, (
TBDPhos)NiCl
(1) and (
TBDPhos)PdCl
(3) react with H
O, alcohols, and hydrated fluoride reagents in the presence of NEt
to yield trans H-O or H-F addition across the bridgehead N-B bond. In contrast,
TBDPhos shows no appreciable reactivity when bound to NiCl
(2) and PdCl
(4), which is attributed to the sterically-bulky isopropyl substituents blocking substrate access to boron in the TBD backbone. The new complexes {[(
TBDPhos-H
O)Ni]
(μ-OH)
}Cl
(5), {[(
TBDPhos-H
O)Pd]
(μ-OH)
}Cl
(6), (
TBDPhos-MeOH)NiCl
(7), (
TBDPhos-MeOH)PdCl
(8), (
TBDPhos-C
H
OH)PdCl
(9), and {[(
TBDPhos-HF)Ni]
(μ-OH)
}Cl
(10) were isolated, and all but 6 were structurally characterized by single-crystal XRD. Multinuclear NMR studies revealed that isolated, crystallographically-authenticated samples of 5-9 lose ligand-bound water or alcohol with reappearance of starting materials 1 and 3 when dissolved in NMR solvents. Addition of NEt
attenuated the water and alcohol loss from 5-9 to allow
H,
C,
P, and
B NMR data to be collected for all the compounds, confirming the determined structures. Additional reactivity experiments with NaOMe and fluoride reagents suggested that participation of the bridgehead nitrogen in the TBD backbone is important for promoting reactivity at boron when
TBDPhos is bound to Ni and Pd. The term "cooperative ligand-centered reactivity" (CLR) is proposed to define chemical reactions that appear to require participation of more than one atom on the ligand, such as those reported here.
Details
- Title: Subtitle
- Triaminoborane-bridged diphosphine complexes with Ni and Pd: coordination chemistry, structures, and ligand-centered reactivity
- Creators
- Kyounghoon LeeCourtney M DonahueScott R Daly - University of Iowa
- Resource Type
- Journal article
- Publication Details
- Dalton transactions : an international journal of inorganic chemistry, Vol.46(29), pp.9394-9406
- DOI
- 10.1039/c7dt02144e
- PMID
- 28695953
- ISSN
- 1477-9226
- eISSN
- 1477-9234
- Language
- English
- Date published
- 07/25/2017
- Academic Unit
- Chemistry
- Record Identifier
- 9984216568702771
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