5‐Methylthiophene‐2, 3‐dithiolene Transition Metal Complexes. Issue 24 (22nd May 2014)
- Record Type:
- Journal Article
- Title:
- 5‐Methylthiophene‐2, 3‐dithiolene Transition Metal Complexes. Issue 24 (22nd May 2014)
- Main Title:
- 5‐Methylthiophene‐2, 3‐dithiolene Transition Metal Complexes
- Authors:
- Neves, Ana I. S.
Santos, Isabel C.
Coutinho, Joana T.
Pereira, Laura C. J.
Henriques, Rui T.
Lopes, Elsa B.
Alves, H.
Almeida, Manuel
Belo, Dulce - Other Names:
- Ouahab Lahcène sponsoringEditor.
Mori Takehiko sponsoringEditor. - Abstract:
- Abstract: Transition metal complexes based on the new ligand 5‐methylthiophene‐2, 3‐dithiolate (α‐mtpdt) and Au, Ni, Fe, Co, Cu Pt and Pd were prepared as tetraalkylammonium and tetraarylphosphonium salts and characterised by cyclic voltammetry, X‐ray diffraction, electron paramagnetic resonance (EPR) spectroscopy and magnetic susceptibility measurements. Except for the Cu complex, which forms a four‐metal cluster [Cu4 (α‐mtpdt)3 ] 2–, the metals form complexes of the general formula [M(α‐mtpdt)2 ]. With Au, Ni and Fe, the complexes are directly obtained from the synthesis as monoanionic salts, and the isostructural crystal structures of [ n Bu4 N][Ni(α‐mtpdt)2 ] and [ n Bu4 N][Au(α‐mtpdt)2 ] were solved by single‐crystal X‐ray diffraction. For M = Co, Pt and Pd, both monoanionic and dianionic salts were obtained, and the crystal structures of [Ph4 As]2 [Co(α‐mtpdt)2 ] and [Ph4 As]2 [Pd(α‐mtpdt)2 ] were determined by single‐crystal X‐ray diffraction. The Co compound presents a rare tetrahedral coordination geometry. The oxidation of the monoanionic Ni and Au complexes with iodine leads to stable neutral complexes, which are fairly soluble in common organic solvents such as acetonitrile and dichloromethane. The crystal structure of [Ni(α‐mtpdt)2 ] was solved by single‐crystal X‐ray diffraction. The electrical conductivities of the neutral Ni and Au complexes as polycrystalline compressed pellets are typical of a semiconductor; the room‐temperature conductivities are 5.2 × 10Abstract: Transition metal complexes based on the new ligand 5‐methylthiophene‐2, 3‐dithiolate (α‐mtpdt) and Au, Ni, Fe, Co, Cu Pt and Pd were prepared as tetraalkylammonium and tetraarylphosphonium salts and characterised by cyclic voltammetry, X‐ray diffraction, electron paramagnetic resonance (EPR) spectroscopy and magnetic susceptibility measurements. Except for the Cu complex, which forms a four‐metal cluster [Cu4 (α‐mtpdt)3 ] 2–, the metals form complexes of the general formula [M(α‐mtpdt)2 ]. With Au, Ni and Fe, the complexes are directly obtained from the synthesis as monoanionic salts, and the isostructural crystal structures of [ n Bu4 N][Ni(α‐mtpdt)2 ] and [ n Bu4 N][Au(α‐mtpdt)2 ] were solved by single‐crystal X‐ray diffraction. For M = Co, Pt and Pd, both monoanionic and dianionic salts were obtained, and the crystal structures of [Ph4 As]2 [Co(α‐mtpdt)2 ] and [Ph4 As]2 [Pd(α‐mtpdt)2 ] were determined by single‐crystal X‐ray diffraction. The Co compound presents a rare tetrahedral coordination geometry. The oxidation of the monoanionic Ni and Au complexes with iodine leads to stable neutral complexes, which are fairly soluble in common organic solvents such as acetonitrile and dichloromethane. The crystal structure of [Ni(α‐mtpdt)2 ] was solved by single‐crystal X‐ray diffraction. The electrical conductivities of the neutral Ni and Au complexes as polycrystalline compressed pellets are typical of a semiconductor; the room‐temperature conductivities are 5.2 × 10 –7 and 8.7 × 10 –5 S cm –1, and the activation energies are 325 and 287 meV, respectively. Abstract : A family of transition metal complexes [M(α‐mtpdt)2 ] (M = Au, Ni, Fe, Cu, Co, Pt and Pd) with a methyl‐substituted thiophenedithiolene ligand (α‐mtpdt) are synthesised. The Ni and Au complexes can be obtained in their neutral state as stable compounds; they are fairly soluble in organic solvents and have semiconducting properties. … (more)
- Is Part Of:
- European journal of inorganic chemistry. Issue 24(2014)
- Journal:
- European journal of inorganic chemistry
- Issue:
- Issue 24(2014)
- Issue Display:
- Volume 24, Issue 24 (2014)
- Year:
- 2014
- Volume:
- 24
- Issue:
- 24
- Issue Sort Value:
- 2014-0024-0024-0000
- Page Start:
- 3989
- Page End:
- 3999
- Publication Date:
- 2014-05-22
- Subjects:
- Dithiolene complexes -- S ligands -- Coordination chemistry -- Cyclic voltammetry -- Magnetic properties
Chemistry, Inorganic -- Periodicals
Organometallic chemistry -- Periodicals
Bioinorganic chemistry -- Periodicals
Solid state chemistry -- Periodicals
546 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ejic.201402048 ↗
- Languages:
- English
- ISSNs:
- 1434-1948
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.730450
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1425.xml