Tungsten and molybdenum dinitrogen complexes supported by a pentadentate tetrapodal phosphine ligand: comparative spectroscopic, electrochemical and reactivity studies. Issue 16 (18th March 2022)
- Record Type:
- Journal Article
- Title:
- Tungsten and molybdenum dinitrogen complexes supported by a pentadentate tetrapodal phosphine ligand: comparative spectroscopic, electrochemical and reactivity studies. Issue 16 (18th March 2022)
- Main Title:
- Tungsten and molybdenum dinitrogen complexes supported by a pentadentate tetrapodal phosphine ligand: comparative spectroscopic, electrochemical and reactivity studies
- Authors:
- Junge, Jannik
Froitzheim, Sven
Engesser, Tobias A.
Krahmer, Jan
Näther, Christian
Le Poul, Nicolas
Tuczek, Felix - Abstract:
- Abstract : The tungsten dinitrogen complex [W(N2 )(P Me 2 PP Ph 2 )] is compared to its molybdenum analogue. Detailed (IR-spectro)electrochemical investigations were made. In the presence of SmI2 /H2 O the W complex mediates the conversion of N2 to 2.75 equiv. ammonia. Abstract : The tungsten dinitrogen complex [W(N2 )(P Me 2 PP Ph 2 )] (2 ) (P Me 2 PP Ph 2 = [2-({bis[3-(diphenylphosphino)propyl]-phosphino}methyl)-2-methylpropane-1, 3-diyl]bis(dimethylphosphine)) is synthesized and characterized by X-ray diffraction as well as IR and NMR spectroscopies, showing strong analogies to its molybdenum analogue [Mo(N2 )(P Me 2 PP Ph 2 )] (1 ). Whereas cyclic voltammetry studies indicate very similar redox potentials, detailed electrochemical and IR-spectroelectrochemical investigations reveal characteristic differences between 1 and 2 upon electrochemical oxidation in THF. Protonation of 2 with HBAr F (BAr F = tetrakis(3, 5-bis(trifluoromethyl)-phenyl)borate) leads to the hydrazido(2-) derivative 3 which is spectroscopically characterized as well. In the presence of SmI2 /H2 O slightly overstoichiometric conversion of N2 to ammonia (2.75 equiv.) is observed. Although this is far below the activity of the Mo-complex 1, it renders 2 the first W complex to produce more than 2 equivalents of NH3 from N2 upon addition of protons and reductant.
- Is Part Of:
- Dalton transactions. Volume 51:Issue 16(2022)
- Journal:
- Dalton transactions
- Issue:
- Volume 51:Issue 16(2022)
- Issue Display:
- Volume 51, Issue 16 (2022)
- Year:
- 2022
- Volume:
- 51
- Issue:
- 16
- Issue Sort Value:
- 2022-0051-0016-0000
- Page Start:
- 6166
- Page End:
- 6176
- Publication Date:
- 2022-03-18
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1dt04212b ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21414.xml