N‐Heterocyclic Carbene–Phosphinidene Complexes of the Coinage Metals. Issue 45 (14th September 2015)
- Record Type:
- Journal Article
- Title:
- N‐Heterocyclic Carbene–Phosphinidene Complexes of the Coinage Metals. Issue 45 (14th September 2015)
- Main Title:
- N‐Heterocyclic Carbene–Phosphinidene Complexes of the Coinage Metals
- Authors:
- Doddi, Adinarayana
Bockfeld, Dirk
Nasr, Alexandre
Bannenberg, Thomas
Jones, Peter G.
Tamm, Matthias - Abstract:
- Abstract: Coinage metal complexes of the N‐heterocyclic carbene–phosphinidene adduct IPr⋅ PPh (IPr=1, 3‐bis(2, 6‐diisopropylphenyl)imidazolin‐2‐ylidene) were prepared by its reaction with CuCl, AgCl, and [(Me2 S)AuCl], which afforded the monometallic complexes [(IPr⋅ PPh)MCl] (M=Cu, Ag, Au). The reaction with two equivalents of the metal halides gave bimetallic [(IPr⋅ PPh)(MCl)2 ] (M=Cu, Au); the corresponding disilver complex could not be isolated. [(IPr⋅ PPh)(CuOTf)2 ] was prepared by reaction with copper(I) trifluoromethanesulfonate. Treatment of [(IPr⋅ PPh)(MCl)2 ] (M=Cu, Au) with Na(BAr F ) or AgSbF6 afforded the tetranuclear complexes [(IPr⋅ PPh)2 M4 Cl2 ]X2 (X=BAr F or SbF6 ), which contain unusual eight‐membered M4 Cl2 P2 rings with short cuprophilic or aurophilic contacts along the chlorine‐bridged M⋅⋅⋅M axes. Complete chloride abstraction from [(IPr⋅ PPh)(AuCl)2 ] was achieved with two equivalents of AgSbF6 in the presence of tetrahydrothiophene (THT) to form [(IPr⋅ PPh){Au(THT)}2 ][SbF6 ]2 . The cationic tetra‐ and dinuclear complexes were used as catalysts for enyne cyclization and carbene transfer reactions. Abstract : Dinuclear gold catalysis : Mono‐, bi‐, and tetranuclear coinage metal complexes of an N‐heterocyclic carbene–phosphinidene are reported. Chloride abstraction affords unusual eight‐membered metallacycles, which feature cuprophilic (M=Cu) and aurophilic (M=Au) interactions (see scheme; Dipp=2, 6‐diisopropylphenyl). The cationic gold(I)–phosphinideneAbstract: Coinage metal complexes of the N‐heterocyclic carbene–phosphinidene adduct IPr⋅ PPh (IPr=1, 3‐bis(2, 6‐diisopropylphenyl)imidazolin‐2‐ylidene) were prepared by its reaction with CuCl, AgCl, and [(Me2 S)AuCl], which afforded the monometallic complexes [(IPr⋅ PPh)MCl] (M=Cu, Ag, Au). The reaction with two equivalents of the metal halides gave bimetallic [(IPr⋅ PPh)(MCl)2 ] (M=Cu, Au); the corresponding disilver complex could not be isolated. [(IPr⋅ PPh)(CuOTf)2 ] was prepared by reaction with copper(I) trifluoromethanesulfonate. Treatment of [(IPr⋅ PPh)(MCl)2 ] (M=Cu, Au) with Na(BAr F ) or AgSbF6 afforded the tetranuclear complexes [(IPr⋅ PPh)2 M4 Cl2 ]X2 (X=BAr F or SbF6 ), which contain unusual eight‐membered M4 Cl2 P2 rings with short cuprophilic or aurophilic contacts along the chlorine‐bridged M⋅⋅⋅M axes. Complete chloride abstraction from [(IPr⋅ PPh)(AuCl)2 ] was achieved with two equivalents of AgSbF6 in the presence of tetrahydrothiophene (THT) to form [(IPr⋅ PPh){Au(THT)}2 ][SbF6 ]2 . The cationic tetra‐ and dinuclear complexes were used as catalysts for enyne cyclization and carbene transfer reactions. Abstract : Dinuclear gold catalysis : Mono‐, bi‐, and tetranuclear coinage metal complexes of an N‐heterocyclic carbene–phosphinidene are reported. Chloride abstraction affords unusual eight‐membered metallacycles, which feature cuprophilic (M=Cu) and aurophilic (M=Au) interactions (see scheme; Dipp=2, 6‐diisopropylphenyl). The cationic gold(I)–phosphinidene complexes serve as active catalysts for enyne cycloisomerization and carbene transfer reactions. … (more)
- Is Part Of:
- Chemistry. Volume 21:Issue 45(2015)
- Journal:
- Chemistry
- Issue:
- Volume 21:Issue 45(2015)
- Issue Display:
- Volume 21, Issue 45 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 45
- Issue Sort Value:
- 2015-0021-0045-0000
- Page Start:
- 16178
- Page End:
- 16189
- Publication Date:
- 2015-09-14
- Subjects:
- carbene ligands -- coinage metals -- copper -- gold -- phosphinidene
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201502208 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23604.xml