Decarbonylation along with P‐atom transfer from the phosphaethynolate anion, PCO−, to the NbIVcomplex [(PNP)NbCl2(N
- Award ID(s):
- 2154620
- PAR ID:
- 10416224
- Date Published:
- Journal Name:
- Chemical Communications
- Volume:
- 58
- Issue:
- 84
- ISSN:
- 1359-7345
- Page Range / eLocation ID:
- 11795 to 11798
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract t BuAr)] (1 ) (PNP=N[2‐Pi Pr2‐4‐methylphenyl]2−; Ar=3,5‐Me2C6H3) results in its coupling with one of the phosphine arms of the pincer ligand to produce a phosphanylidene phosphorane complex [(PNPP)NbCl(Nt BuAr)] (2 ). Reduction of2 with CoCp*2cleaves the P−P bond to form the first neutral and terminal phosphido complex of a group 5 transition metal, namely, [(PNP)Nb≡P(Nt BuAr)] (3 ). Theoretical studies have been used to understand both the coupling of the P‐atom and the reductive cleavage of the P−P bond. Reaction of3 with a two‐electron oxidant such as ethylene sulfide results in a diamagnetic sulfido complex having a P−P coupled ligand, namely [(PNPP)Nb=S(Nt BuAr)] (4 ). -
Abstract Decarbonylation along with P‐atom transfer from the phosphaethynolate anion, PCO−, to the NbIVcomplex [(PNP)NbCl2(N
t BuAr)] (1 ) (PNP=N[2‐Pi Pr2‐4‐methylphenyl]2−; Ar=3,5‐Me2C6H3) results in its coupling with one of the phosphine arms of the pincer ligand to produce a phosphanylidene phosphorane complex [(PNPP)NbCl(Nt BuAr)] (2 ). Reduction of2 with CoCp*2cleaves the P−P bond to form the first neutral and terminal phosphido complex of a group 5 transition metal, namely, [(PNP)Nb≡P(Nt BuAr)] (3 ). Theoretical studies have been used to understand both the coupling of the P‐atom and the reductive cleavage of the P−P bond. Reaction of3 with a two‐electron oxidant such as ethylene sulfide results in a diamagnetic sulfido complex having a P−P coupled ligand, namely [(PNPP)Nb=S(Nt BuAr)] (4 ). -
We report the synthesis of molybdenum and tungsten bromo dicarbonyl complexes (POCOPtBu)MIIBr(CO)2(M = Mo or W; POCOPtBu = κ3-C6H3-1,3-[OP( tBu)2]2) supported by an anionic PCP pincer ligand, and the chromium complex (PNPtBu)Cr0(CO)3(PNPtBu = 2,6-bis(di- tert-butyl-phosphinomethyl)pyridine) bearing a neutral PNP pincer scaffold. The three group six complexes described in this study have been characterized by Liquid Injection Field Desorption Ionization Mass Spectrometry (LIFDI-MS), NMR, and IR spectroscopy. Single crystal X-ray diffraction studies show the MoIIand WIIcomplexes adopt a six-coordinate distorted trigonal prismatic geometry, whereas the Cr0complex exhibits a distorted octahedral geometry.
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null (Ed.)The bis(imido) complexes (BDI)Nb(N t Bu) 2 and (BDI)Nb(N t Bu)(NAr) (BDI = N , N ′-bis(2,6-diisopropylphenyl)-3,5-dimethyl-β-diketiminate; Ar = 2,6-diisopropylphenyl) were shown to engage in 1,2-addition and [2 + 2] cycloaddition reactions with a wide variety of substrates. Reaction of the bis(imido) complexes with dihydrogen, silanes, and boranes yielded hydrido-amido-imido complexes via 1,2-addition across Nb-imido π-bonds; some of these complexes were shown to further react via insertion of carbon dioxide to give formate-amido-imido products. Similarly, reaction of (BDI)Nb(N t Bu) 2 with tert -butylacetylene yielded an acetylide-amido-imido complex. In contrast to these results, many related mono(imido) Nb BDI complexes do not exhibit 1,2-addition reactivity, suggesting that π-loading plays an important role in activating the Nb–N π-bonds toward addition. The same bis(imido) complexes were also shown to engage in [2 + 2] cycloaddition reactions with oxygen- and sulfur-containing heteroallenes to give carbamate- and thiocarbamate-imido complexes: some of these complexes readily dimerized to give bis-μ-sulfido, bis-μ-iminodicarboxylate, and bis-μ-carbonate complexes. The mononuclear carbamate imido complex (BDI)Nb(NAr)(N( t Bu)CO 2 ) ( 12 ) could be induced to eject tert -butylisocyanate to generate a four-coordinate terminal oxo imido intermediate, which could be trapped as the five-coordinate pyridine or DMAP adduct. The DMAP adducted oxo imido complex (BDI)NbO(NAr)(DMAP) ( 16 ) was shown to engage in 1,2-addition of silanes across the Nb-oxo π-bond; this represents a new reaction pathway in group 5 chemistry.more » « less
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null (Ed.)Reaction of LiOC t Bu 2 Ph with TlPF 6 forms the dimeric Tl 2 (OC t Bu 2 Ph) 2 complex, a rare example of a homoleptic thallium alkoxide complex demonstrating formally two-coordinate metal centers. Characterization of Tl 2 (OC t Bu 2 Ph) 2 by 1 H and 13 C NMR spectroscopy and X-ray crystallography reveals the presence of two isomers differing by the mutual conformation of the alkoxide ligands, and by the planarity of the central Tl–O–Tl–O plane. Tl 2 (OC t Bu 2 Ph) 2 serves as a convenient precursor to the formation of old and new [M(OC t Bu 2 Ph) n ] complexes (M = Cr, Fe, Cu, Zn), including a rare example of T-shaped Zn(OC t Bu 2 Ph) 2 (THF) complex, which could not be previously synthesized using more conventional LiOR/HOR precursors. The reaction of [Ru(cymene)Cl 2 ] 2 with Tl 2 (OC t Bu 2 Ph) 2 results in the formation of a ruthenium( ii ) alkoxide complex. For ruthenium, the initial coordination of the alkoxide triggers C–H activation at the ortho -H of [OC t Bu 2 Ph] which results in its bidentate coordination. In addition to Tl 2 (OC t Bu 2 Ph) 2 , related Tl 2 (OC t Bu 2 (3,5-Me 2 C 6 H 3 )) 2 was also synthesized, characterized, and shown to exhibit similar reactivity with iron and ruthenium precursors. Synthetic, structural, and spectroscopic characterizations are presented.more » « less