Preparation of monocarbonyl ruthenium complexes bearing bidentate nitrogen and phosphine ligands and their catalytic activity in carbonyl compound reduction. Issue 33 (1st August 2019)
- Record Type:
- Journal Article
- Title:
- Preparation of monocarbonyl ruthenium complexes bearing bidentate nitrogen and phosphine ligands and their catalytic activity in carbonyl compound reduction. Issue 33 (1st August 2019)
- Main Title:
- Preparation of monocarbonyl ruthenium complexes bearing bidentate nitrogen and phosphine ligands and their catalytic activity in carbonyl compound reduction
- Authors:
- Giboulot, Steven
Comuzzi, Clara
Del Zotto, Alessandro
Figliolia, Rosario
Lippe, Giovanna
Lovison, Denise
Strazzolini, Paolo
Susmel, Sabina
Zangrando, Ennio
Zuccaccia, Daniele
Baldino, Salvatore
Ballico, Maurizio
Baratta, Walter - Abstract:
- Abstract : A series of novel monocarbonyl ruthenium catalysts containing bidentate dinitrogen or/and diphosphine ligands are easily obtained through a general and straightforward approach. Abstract : Monocarbonyl complexes [RuCl2 (CO)(PR3 )(NN)] (R = Cy, NN = en1, ampy2 ; R = iPr; NN = en3 ) have been prepared in a one pot reaction from [RuCl2 (CO)(dmf)(PPh3 )2 ], PR3 and the NN ligand in CH2 Cl2 . Treatment of [Ru(OAc)2 (CO)(PPh3 )2 ] with NN ligands in methanol gives the cationic derivatives [Ru(OAc)(CO)(PPh3 )(NN)]OAc (NN = en4, ampy5 ) in which one acetate acts as a bidentate ligand, whereas the other is not coordinated. Diphosphine complexes [RuCl2 (CO)(PP)(PPh3 )] (PP = dppb6, dppf7, ( R )-BINAP8, ( R, S p )-Josiphos9 and ( R, R )-Skewphos10 ) have been obtained starting from [RuCl2 (CO)(dmf)(PPh3 )2 ] and the PP ligand in CHCl3 or toluene at reflux. The reaction of [Ru(OAc)2 (CO)(PPh3 )2 ] with PP in CH2 Cl2 or toluene affords the fluxional acetate derivatives [Ru(OAc)2 (CO)(PP)] (PP = dppb11, dppf12, ( R )-BINAP13, and ( R, R )-Skewphos14 ). The cationic diphosphine complexes [RuCl(CO)(PP)(en)]Cl (PP = dppb15, dppf16 ) are prepared from [RuCl2 (CO)(dmf)(PPh3 )2 ], PP and en in CH2 Cl2 or, alternatively, from [RuCl2 (CO)2 ] n or the6, 7 derivatives. Similarly, [Ru(OAc)(CO)(PP)(NN)]OAc (PP = dppb, NN = en17, ampy18 ; PP = dppf, NN = en19, ampy20 ) are isolated starting from [Ru(OAc)2 (CO)(PPh3 )2 ], PP and NN ligands or from11, 12 . The derivatives [Ru(OAc)2 (CO)(PP)]Abstract : A series of novel monocarbonyl ruthenium catalysts containing bidentate dinitrogen or/and diphosphine ligands are easily obtained through a general and straightforward approach. Abstract : Monocarbonyl complexes [RuCl2 (CO)(PR3 )(NN)] (R = Cy, NN = en1, ampy2 ; R = iPr; NN = en3 ) have been prepared in a one pot reaction from [RuCl2 (CO)(dmf)(PPh3 )2 ], PR3 and the NN ligand in CH2 Cl2 . Treatment of [Ru(OAc)2 (CO)(PPh3 )2 ] with NN ligands in methanol gives the cationic derivatives [Ru(OAc)(CO)(PPh3 )(NN)]OAc (NN = en4, ampy5 ) in which one acetate acts as a bidentate ligand, whereas the other is not coordinated. Diphosphine complexes [RuCl2 (CO)(PP)(PPh3 )] (PP = dppb6, dppf7, ( R )-BINAP8, ( R, S p )-Josiphos9 and ( R, R )-Skewphos10 ) have been obtained starting from [RuCl2 (CO)(dmf)(PPh3 )2 ] and the PP ligand in CHCl3 or toluene at reflux. The reaction of [Ru(OAc)2 (CO)(PPh3 )2 ] with PP in CH2 Cl2 or toluene affords the fluxional acetate derivatives [Ru(OAc)2 (CO)(PP)] (PP = dppb11, dppf12, ( R )-BINAP13, and ( R, R )-Skewphos14 ). The cationic diphosphine complexes [RuCl(CO)(PP)(en)]Cl (PP = dppb15, dppf16 ) are prepared from [RuCl2 (CO)(dmf)(PPh3 )2 ], PP and en in CH2 Cl2 or, alternatively, from [RuCl2 (CO)2 ] n or the6, 7 derivatives. Similarly, [Ru(OAc)(CO)(PP)(NN)]OAc (PP = dppb, NN = en17, ampy18 ; PP = dppf, NN = en19, ampy20 ) are isolated starting from [Ru(OAc)2 (CO)(PPh3 )2 ], PP and NN ligands or from11, 12 . The derivatives [Ru(OAc)2 (CO)(PP)] show a fluxional behavior in solution as the result of the flexible coordination of acetate ligands. These complexes are found to be active in the transfer hydrogenation and hydrogenation of ketones and aldehydes, including furfural derivatives, at an S/C up to 10 000 and a TOF up to 18 000 h −1 . … (more)
- Is Part Of:
- Dalton transactions. Volume 48:Issue 33(2019)
- Journal:
- Dalton transactions
- Issue:
- Volume 48:Issue 33(2019)
- Issue Display:
- Volume 48, Issue 33 (2019)
- Year:
- 2019
- Volume:
- 48
- Issue:
- 33
- Issue Sort Value:
- 2019-0048-0033-0000
- Page Start:
- 12560
- Page End:
- 12576
- Publication Date:
- 2019-08-01
- 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/c9dt02616a ↗
- 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:
- 11436.xml