The First Molybdenum(VI) and Tungsten(VI) Oxoazides MO2(N3)2, MO2(N3)2⋅2 CH3CN, (bipy)MO2(N3)2, and [MO2(N3)4]2− (M=Mo, W)1. (14th July 2015)
- Record Type:
- Journal Article
- Title:
- The First Molybdenum(VI) and Tungsten(VI) Oxoazides MO2(N3)2, MO2(N3)2⋅2 CH3CN, (bipy)MO2(N3)2, and [MO2(N3)4]2− (M=Mo, W)1. (14th July 2015)
- Main Title:
- The First Molybdenum(VI) and Tungsten(VI) Oxoazides MO2(N3)2, MO2(N3)2⋅2 CH3CN, (bipy)MO2(N3)2, and [MO2(N3)4]2− (M=Mo, W)1
- Authors:
- Haiges, Ralf
Skotnitzki, Juri
Fang, Zongtang
Dixon, David A.
Christe, Karl O. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Molybdenum(VI) and tungsten(VI) dioxodiazide, MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> (M=Mo, W), were prepared through fluoride–azide exchange reactions between MO<sub>2</sub>F<sub>2</sub> and Me<sub>3</sub>SiN<sub>3</sub> in SO<sub>2</sub> solution. In acetonitrile solution, the fluoride–azide exchange resulted in the isolation of the adducts MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>⋅2 CH<sub>3</sub>CN. The subsequent reaction of MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> with 2, 2′‐bipyridine (bipy) gave the bipyridine adducts (bipy)MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>. The hydrolysis of (bipy)MoO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> resulted in the formation and isolation of [(bipy)MoO<sub>2</sub>N<sub>3</sub>]<sub>2</sub>O. The tetraazido anions [MO<sub>2</sub>(N<sub>3</sub>)<sub>4</sub>]<sup>2−</sup> were obtained by the reaction of MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> with two equivalents of ionic azide. Most molybdenum(VI) and tungsten(VI) dioxoazides were fully characterized by their vibrational spectra, impact, friction, and thermal sensitivity data and, in the case of (bipy)MoO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>, (bipy)WO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>, [PPh<sub>4</sub>]<sub>2</sub>[MoO<sub>2</sub>(N<sub>3</sub>)<sub>4</sub>], [PPh<sub>4</sub>]<sub>2</sub>[WO<sub>2</sub>(N<sub>3</sub>)<sub>4</sub>], and [(bipy)MoO<sub>2</sub>N<sub>3</sub>]<sub>2</sub>O by their X‐ray<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Molybdenum(VI) and tungsten(VI) dioxodiazide, MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> (M=Mo, W), were prepared through fluoride–azide exchange reactions between MO<sub>2</sub>F<sub>2</sub> and Me<sub>3</sub>SiN<sub>3</sub> in SO<sub>2</sub> solution. In acetonitrile solution, the fluoride–azide exchange resulted in the isolation of the adducts MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>⋅2 CH<sub>3</sub>CN. The subsequent reaction of MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> with 2, 2′‐bipyridine (bipy) gave the bipyridine adducts (bipy)MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>. The hydrolysis of (bipy)MoO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> resulted in the formation and isolation of [(bipy)MoO<sub>2</sub>N<sub>3</sub>]<sub>2</sub>O. The tetraazido anions [MO<sub>2</sub>(N<sub>3</sub>)<sub>4</sub>]<sup>2−</sup> were obtained by the reaction of MO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub> with two equivalents of ionic azide. Most molybdenum(VI) and tungsten(VI) dioxoazides were fully characterized by their vibrational spectra, impact, friction, and thermal sensitivity data and, in the case of (bipy)MoO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>, (bipy)WO<sub>2</sub>(N<sub>3</sub>)<sub>2</sub>, [PPh<sub>4</sub>]<sub>2</sub>[MoO<sub>2</sub>(N<sub>3</sub>)<sub>4</sub>], [PPh<sub>4</sub>]<sub>2</sub>[WO<sub>2</sub>(N<sub>3</sub>)<sub>4</sub>], and [(bipy)MoO<sub>2</sub>N<sub>3</sub>]<sub>2</sub>O by their X‐ray crystal structures.</p> </abstract> … (more)
- Is Part Of:
- Angewandte Chemie. Volume 127:Number 33(2015)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 127:Number 33(2015)
- Issue Display:
- Volume 127, Issue 33 (2015)
- Year:
- 2015
- Volume:
- 127
- Issue:
- 33
- Issue Sort Value:
- 2015-0127-0033-0000
- Page Start:
- 9717
- Page End:
- 9721
- Publication Date:
- 2015-07-14
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.201504629 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4348.xml