Addition of sub‐stoichiometric quantities of PEt3and diphenyl disulfide to a solution of [Ni(1,5‐cod)2] generates a mixture of [Ni3(SPh)4(PEt3)3] (
The 1 : 2 reaction of the imidazole‐based dithiolate (
- Award ID(s):
- 2153978
- PAR ID:
- 10468822
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Chemistry – A European Journal
- Volume:
- 29
- Issue:
- 65
- ISSN:
- 0947-6539
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract 1 ), unreacted [Ni(1,5‐cod)2], and [(1,5‐cod)Ni(PEt3)2], according to1H and31P{1H} NMR spectroscopic monitoring of the in situ reaction mixture. On standing, complex1 converts into [Ni4(S)(Ph)(SPh)3(PEt3)3] (2 ), via formal addition of a “Ni(0)” equivalent, coupled with a CS oxidative addition step, which simultaneously generates the Ni‐bound phenyl ligand and the μ3‐sulfide ligand. Upon gentle heating, complex2 converts into a mixture of [Ni5(S)2(SPh)2(PEt3)5] (3 ) and [Ni8(S)5(PEt3)7] (4 ), via further addition of “Ni(0)” equivalents, in combination with a series of C–S oxidative addition and CC reductive elimination steps, which serve to convert thiophenolate ligands into sulfide ligands and biphenyl. The presence of1 –4 in the reaction mixture is confirmed by their independent syntheses and subsequent spectroscopic characterization. Overall, this work provides an unprecedented level of detail of the early stages of Ni nanocluster growth and highlights the fundamental reaction steps (i.e., metal atom addition, CS oxidative addition, and CC reductive elimination) that are required to grow an individual cluster. -
Abstract Whereas low‐temperature (−78 °C) reaction of the lithium dithiolene radical
1 .with boron bromide gives the dibromoboron dithiolene radical2 ., the parallel reaction of1 .with (C6H11)2BCl (0 °C) affords the dicyclohexylboron dithiolene radical3 .. Radicals2 .and3 .were characterized by single‐crystal X‐ray diffraction, UV/Vis, and EPR spectroscopy. The nature of these radicals was also probed computationally. Under mild conditions,3 .undergoes unexpected thiourea‐mediated B−C bond activation to give zwitterion4 , which may be regarded as an anionic dithiolene‐modified carbene complex of the sulfenyl cation RS+(R=cyclohexyl). -
Abstract Whereas low‐temperature (−78 °C) reaction of the lithium dithiolene radical
1 .with boron bromide gives the dibromoboron dithiolene radical2 ., the parallel reaction of1 .with (C6H11)2BCl (0 °C) affords the dicyclohexylboron dithiolene radical3 .. Radicals2 .and3 .were characterized by single‐crystal X‐ray diffraction, UV/Vis, and EPR spectroscopy. The nature of these radicals was also probed computationally. Under mild conditions,3 .undergoes unexpected thiourea‐mediated B−C bond activation to give zwitterion4 , which may be regarded as an anionic dithiolene‐modified carbene complex of the sulfenyl cation RS+(R=cyclohexyl). -
Abstract The structures and magnetic properties of four paramagnetic bis(carbene)niobium and a diamagnetic monocarbene complex are described. Crystallographic studies show solvated crystals of NbCl4(IMes)2(
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