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| Home > Publications database > Volatile Rhenium(I) Compounds with Re–N Bonds and Their Conversion into Oriented Rhenium Nitride Films by Magnetic Field-Assisted Vapor Phase Deposition > print |
| Home > Publications database > Volatile Rhenium(I) Compounds with Re–N Bonds and Their Conversion into Oriented Rhenium Nitride Films by Magnetic Field-Assisted Vapor Phase Deposition > print |
| 001 | 864457 | ||
| 005 | 20230310131317.0 | ||
| 024 | 7 | _ | |a 10.1021/acs.inorgchem.9b01656 |2 doi |
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| 100 | 1 | _ | |a Frank, Michael |0 0000-0003-3217-9570 |b 0 |
| 245 | _ | _ | |a Volatile Rhenium(I) Compounds with Re–N Bonds and Their Conversion into Oriented Rhenium Nitride Films by Magnetic Field-Assisted Vapor Phase Deposition |
| 260 | _ | _ | |a Washington, DC |c 2019 |b American Chemical Society |
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| 520 | _ | _ | |a New heteroleptic rhenium(I) compounds, [fac-Re(I)(CO)3(L)] (e.g., L= tfb-dmpda, (N,N-(4,4,4-trifluorobut-1-en-3-on)-dimethyl propylene diamine)), containing anionic and neutral ligands act as efficient precursors to grow polycrystalline rhenium nitride (ReN) films by their vapor phase deposition at 600 °C. Deposition of ReN films under an external magnetic field showed an orientation effect with preferred growth of crystallites along ⟨100⟩ direction. Rhenium complexes reported here unify high stability and reactivity in a single molecule through a Janus-type coordination around a Re center, constituted by a chelating tridentate ligand and three carbonyl groups imparting a facial geometry. Single-crystal diffraction analysis confirmed the structural integrity of the new rhenium compounds. The rigidity of molecular framework was validated in solution via 1D and 2D NMR spectroscopy, in the gas phase via mass spectrometry, and in the solid-state by thermogravimetric analysis and differential scanning calorimetry studies. The analytical data showed that pre-existent Re–N bonds in [fac-Re(I)(CO)3(L)] facilitated low-temperature formation of crystalline ReN deposits confirmed by grazing angle X-ray diffraction analysis. The surface chemical composition and the uniformity of microstructure were provided by X-ray photoelectron spectroscopy (XPS) and scanning and transmission electron microscopy (SEM/TEM), respectively. |
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| 700 | 1 | _ | |a Jürgensen, Lasse |0 0000-0002-8385-9886 |b 1 |
| 700 | 1 | _ | |a Leduc, Jennifer |0 0000-0002-5222-241X |b 2 |
| 700 | 1 | _ | |a Stadler, Daniel |0 P:(DE-HGF)0 |b 3 |
| 700 | 1 | _ | |a Graf, David |0 P:(DE-HGF)0 |b 4 |
| 700 | 1 | _ | |a Gessner, Isabel |0 P:(DE-HGF)0 |b 5 |
| 700 | 1 | _ | |a Zajusch, Fabian |0 P:(DE-HGF)0 |b 6 |
| 700 | 1 | _ | |a Fischer, Thomas |0 0000-0002-8363-9613 |b 7 |
| 700 | 1 | _ | |a Rose, Marc-André |0 P:(DE-Juel1)172846 |b 8 |
| 700 | 1 | _ | |a Müller, David |0 P:(DE-Juel1)166093 |b 9 |
| 700 | 1 | _ | |a Mathur, Sanjay |0 0000-0003-2765-2693 |b 10 |e Corresponding author |
| 773 | _ | _ | |a 10.1021/acs.inorgchem.9b01656 |g Vol. 58, no. 15, p. 10408 - 10416 |0 PERI:(DE-600)1484438-2 |n 15 |p 10408 - 10416 |t Inorganic chemistry |v 58 |y 2019 |x 1520-510X |
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