0000000000240327
AUTHOR
J. Sala Pala
Molecular hybrids formed by oxalate bridged dinuclear anions and organometallic cations
Abstract The syntheses, magnetic properties and infrared spectra of a new series of molecular hybrids formed by association of two magnetic sublattices: (i) oxalate bridged dinuclear anions [V 2 O 2 (ox)(NCS) 6 ] 4− and [M′M′'(ox)(NCS) 8 ] 4 ( M′= Fe III , Cr III ; M′' - Fe III , Cr III ; ox 2 = C 2 O 4 2 and (ii) decamethylferrocenium organometallic cation are presented. The crystal structure of [Fe(Cp * ) 2 ][(C 2 H 5 ) 4 N] 2 [V 2 O 2 (ox)(NCS) 6 ] is also discussed.
Molecular materials based upon organic π-donors and magnetic anions
Electrochemical combination of the magnetic dinuclear anion [MM'(C 2 O 4 )(NCS) 8 ] 4- (MM' = CrCr, CrFe) or paramagnetic mononuclear anion [Cr(NCS) 6 ] 3- with the ET organic π-donor (ET = BEDT-TTF = bis(ethylenedithio)tetrathiafulvalene) gives rise to two new series of molecular hybrid salts formulated (ET) 5 [MM'(C 2 O 4 )(NCS) 8 (MM' = CrCr (1), CrFe (2)), (ET) 8 [MM'(C 2 O 4 )(NCS) 8 ] (3), (ET) 5.5 f Cr(NCS) 6 ] (4) and (ET) 5 [(C 2 H 5 ) 4 N] [Cr(NCS) 6 ](THF) (5) (THF = tetrahydrofuran). The crystal structures consist of alternating organic and inorganic layers. The organic part does not produce any detectable effect on the magnetic properties coming from the inorganic sublattice. T…
Radical cation salts based on BEDT-TTF and the paramagnetic anion [Cr(NCS)6]3−
Abstract A new radical cation salt formulated as (ET)5.5[Cr(NCS)6] (ET = BEDT-TTF = bis(ethylene)dithiotetrathiafulvalene) has been synthesised and characterised by X-ray diffraction and magnetic measurements. The structure shows the presence of alternating layers of the ET units and mixed layers of anions and an isolated ET molecule. The magnetic susceptibility data in the temperature range 2–300 K show a Curie law with C = 1.771 cm3.K.mol−1 and Nα = 1.20.10−5 cm3.mol−1, in agreement with the presence of isolated Cr(III) without any contribution from the organic part.
A two-dimensional magnetic architecture with bridging polynitrile and 2,2′-bipyrimidine ligands
cited By 7; International audience; A new polymeric, two-dimensional compound [Co2(bpym)(dcne) 4 (H2O)2] (1) (dcne = [(CN)2CC(O) OEt)]- = 2,2-dicyano-1-ethoxyethenolate anion and bpym = 2,2'-bipyrimidine) has been synthesized and characterized by X-ray crystallography. The structure is monoclinic space group P21/a and consists of two-dimensional networks of octahedrally coordinated Co(II) ions, bridged by bis-bidentate 2,2'-bipyrimidine and μ2-dcne anions. Magnetic measurements revealed a broad maximum in the xm vs T plot at 20 K which is characteristic of antiferromagnetic exchange between the high spin cobalt(II) centres. © EDP Sciences.
Polynitrile anions as ligands: Synthesis, structure and magnetic properties of a new three-dimensional coordination polymer with the 2-dicyanomethylene-1,1,3,3-tetracyanopropanediide (tcpd2-) bridging ligand
cited By 12; International audience; Reaction between CuCl2 and K2tcpd (tcpd2- = C[C(CN)2]32- = 2-dicyanomethylenc-1,1,3,3-tetracyanopropanediide anion) in presence of the neutral ligand tn (1,3-diaminopropane) in aqueous solution yields the new compound [Cu(tn)(tcpd)] (1) which was characterized by X-ray crystallography. The crystal structure of 1 consists of one [Cu(tn)]2+ unit and one tcpd2- anion, both located on general positions. Each Cu atom presents an essentially octahedral coordination with four nitrogen atoms arising from four polynitrile ligands and two nitrogen atoms from the chelating tn ligand. Despite its six nitrile groups potentially bridging, the tcpd ligand acts with a μ…
Two bimetallic layered materials with “Cu4Fe3” defective cubane units: syntheses, structures and magnetic properties of {[CuII(tn)]2[FeII(CN)6]}3·[Na3FeIII(CN)6]·12H2O (1) and {[CuII(tn)]2[FeII(CN)6]}·KCl·5H2O(2)
Abstract Reactions of the [Fe III (CN) 6 ] 3− anion with the [Cu II (tn)] 2+ ion (tn = 1,3-diaminopropane) afford the compounds {[Cu II (tn)] 2 [Fe II (CN) 6 ]}3·[Na 3 Fe III (CN) 6 ]·12H 2 O (1) and {[Cu n (tn)] 2 [Fe II (CN) 6 ]}·KCl·5H 2 O (2). Despite the differences concerning their asymmetric units, both structures present strong similar features: in both structures, the Cu(II) ion presents a square-base pyramidal CuN 5 environment and each [Fe II (CN) 6 ] 4− anion is linked to six Cu(II) ions through its six N atoms leading to infinite [Cu II (tn)] 2 [Fe II (CN) 6 ] layers which can be viewed as 2-D layered arrangement generated by the defective cubane units Cu 4 Fe 3 involving Fe-CN…