Heterodimetallic Structures Based on Cyano-Substituted Bis(dithiolene) Complexes and Ni and Cu Cyclam Cations

Five charge‐transfer salts based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni, Cu) cations, namely, [Ni(cyclam)]2[Cu(dcbdt)2]2·4DMF (1, dcbdt = 4,5‐dicyanobenzene‐1,2‐dithiolate, DMF = N,N‐dimethylformamide), [Ni(cyclam)]...

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Vydáno v:European journal of inorganic chemistry Ročník 2013; číslo 26; s. 4612 - 4618
Hlavní autoři: Cerdeira, Ana C., Belo, Dulce, Rabaça, Sandra, Pereira, Laura C. J., Coutinho, Joana T., Simão, Dulce, Henriques, Rui T., Jeannin, Olivier, Fourmigué, Marc, Almeida, Manuel
Médium: Journal Article
Jazyk:angličtina
Vydáno: Weinheim WILEY-VCH Verlag 03.09.2013
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ISSN:1434-1948, 1099-0682
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Abstract Five charge‐transfer salts based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni, Cu) cations, namely, [Ni(cyclam)]2[Cu(dcbdt)2]2·4DMF (1, dcbdt = 4,5‐dicyanobenzene‐1,2‐dithiolate, DMF = N,N‐dimethylformamide), [Ni(cyclam)]2[Cu(dcdmp)2]2·4DMF (2, dcdmp = 2,3‐dicyano‐5,6‐dimercaptopyrazine), [Cu(cyclam)]2[Cu(dcdmp)2]2·4DMF (3), [Cu(cyclam)]2[Fe2(cbdt)4]2·4DMF (4, cbdt = 4‐cyanobenzene‐1,2‐dithiolate) and [Ni(cyclam)]2[Fe2(cbdt)4]2·4DMF (5), were prepared and characterised by X‐ray diffraction and magnetisation measurements. The crystal structures of 1–4 were determined by single‐crystal X‐ray diffraction, which revealed that the cyano groups from dithiolene complexes fail to coordinate the metal ions in the cyclam units. Instead, they are coordinated by solvent molecules or by dithiolene S atoms and cyclam N–H groups, which participate in hydrogen bonds to the nitrile and sulfur moieties in the anions. Heterodimetallic structures based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni, Cu) cations display a new coordination mode of the dithiolene S atom towards the metal cyclam.
AbstractList Five charge-transfer salts based on the combination of anionic Fe super(III) and Cu super(II) bis(dithiolene) complexes containing nitrile groups with [M(cyclam)] super(2+) (M = Ni, Cu) cations, namely, [Ni(cyclam)] sub(2)[Cu(dcbdt) sub(2)] sub(2).4DMF (1, dcbdt = 4,5-dicyanobenzene-1,2-dithiolate, DMF = N,N-dimethylformamide), [Ni(cyclam)] sub(2)[Cu(dcdmp) sub(2)] sub(2).4DMF (2, dcdmp = 2,3-dicyano-5,6-dimercaptopyrazine), [Cu(cyclam)] sub(2)[Cu(dcdmp) sub(2)] sub(2).4DMF (3), [Cu(cyclam)] sub(2)[Fe sub(2)(cbd t) sub(4)] sub(2).4DMF (4, cbdt = 4-cyanobenzene-1,2-dithiolate) and [Ni(cyclam)] sub(2)[Fe sub(2)(cbd t) sub(4)] sub(2).4DMF (5), were prepared and characterised by X-ray diffraction and magnetisation measurements. The crystal structures of 1-4 were determined by single-crystal X-ray diffraction, which revealed that the cyano groups from dithiolene complexes fail to coordinate the metal ions in the cyclam units. Instead, they are coordinated by solvent molecules or by dithiolene S atoms and cyclam N-H groups, which participate in hydrogen bonds to the nitrile and sulfur moieties in the anions. Heterodimetallic structures based on the combination of anionic Fe super(III) and Cu super(II) bis(dithiolene) complexes containing nitrile groups with [M(cyclam)] super(2+) (M = Ni, Cu) cations display a new coordination mode of the dithiolene S atom towards the metal cyclam.
Five charge‐transfer salts based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni, Cu) cations, namely, [Ni(cyclam)]2[Cu(dcbdt)2]2·4DMF (1, dcbdt = 4,5‐dicyanobenzene‐1,2‐dithiolate, DMF = N,N‐dimethylformamide), [Ni(cyclam)]2[Cu(dcdmp)2]2·4DMF (2, dcdmp = 2,3‐dicyano‐5,6‐dimercaptopyrazine), [Cu(cyclam)]2[Cu(dcdmp)2]2·4DMF (3), [Cu(cyclam)]2[Fe2(cbdt)4]2·4DMF (4, cbdt = 4‐cyanobenzene‐1,2‐dithiolate) and [Ni(cyclam)]2[Fe2(cbdt)4]2·4DMF (5), were prepared and characterised by X‐ray diffraction and magnetisation measurements. The crystal structures of 1–4 were determined by single‐crystal X‐ray diffraction, which revealed that the cyano groups from dithiolene complexes fail to coordinate the metal ions in the cyclam units. Instead, they are coordinated by solvent molecules or by dithiolene S atoms and cyclam N–H groups, which participate in hydrogen bonds to the nitrile and sulfur moieties in the anions. Heterodimetallic structures based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni, Cu) cations display a new coordination mode of the dithiolene S atom towards the metal cyclam.
Five charge-transfer salts based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni, Cu) cations, namely, [Ni(cyclam)]2[Cu(dcbdt)2]2·4DMF (1, dcbdt = 4,5-dicyanobenzene-1,2-dithiolate, DMF = N,N-dimethylformamide), [Ni(cyclam)]2[Cu(dcdmp)2]2·4DMF (2, dcdmp = 2,3-dicyano-5,6-dimercaptopyrazine), [Cu(cyclam)]2[Cu(dcdmp)2]2·4DMF (3), [Cu(cyclam)]2[Fe2(cbdt)4]2·4DMF (4, cbdt = 4-cyanobenzene-1,2-dithiolate) and [Ni(cyclam)]2[Fe2(cbdt)4]2·4DMF (5), were prepared and characterised by X-ray diffraction and magnetisation measurements. The crystal structures of 1–4 were determined by single-crystal X-ray diffraction, which revealed that the cyano groups from dithiolene complexes fail to coordinate the metal ions in the cyclam units. Instead, they are coordinated by solvent molecules or by dithiolene S atoms and cyclam N–H groups, which participate in hydrogen bonds to the nitrile and sulfur moieties in the anions.
Five charge‐transfer salts based on the combination of anionic Fe III and Cu II bis(dithiolene) complexes containing nitrile groups with [M(cyclam)] 2+ (M = Ni, Cu) cations, namely, [Ni(cyclam)] 2 [Cu(dcbdt) 2 ] 2 · 4DMF ( 1 , dcbdt = 4,5‐dicyanobenzene‐1,2‐dithiolate, DMF = N , N ‐dimethylformamide), [Ni(cyclam)] 2 [Cu(dcdmp) 2 ] 2 · 4DMF ( 2 , dcdmp = 2,3‐dicyano‐5,6‐dimercaptopyrazine), [Cu(cyclam)] 2 [Cu(dcdmp) 2 ] 2 · 4DMF ( 3 ), [Cu(cyclam)] 2 [Fe 2 (cbdt) 4 ] 2 · 4DMF ( 4 , cbdt = 4‐cyanobenzene‐1,2‐dithiolate) and [Ni(cyclam)] 2 [Fe 2 (cbdt) 4 ] 2 · 4DMF ( 5 ), were prepared and characterised by X‐ray diffraction and magnetisation measurements. The crystal structures of 1 – 4 were determined by single‐crystal X‐ray diffraction, which revealed that the cyano groups from dithiolene complexes fail to coordinate the metal ions in the cyclam units. Instead, they are coordinated by solvent molecules or by dithiolene S atoms and cyclam N–H groups, which participate in hydrogen bonds to the nitrile and sulfur moieties in the anions.
Five charge-transfer salts based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni, Cu) cations, namely, [Ni(cyclam)]2[Cu(dcbdt)2]2·4DMF (1, dcbdt = 4,5-dicyanobenzene-1,2-dithiolate, DMF = N,N-dimethylformamide), [Ni(cyclam)]2[Cu(dcdmp)2]2·4DMF (2, dcdmp = 2,3-dicyano-5,6-dimercaptopyrazine), [Cu(cyclam)]2[Cu(dcdmp)2]2·4DMF (3), [Cu(cyclam)]2[Fe2(cbdt)4]2·4DMF (4, cbdt = 4-cyanobenzene-1,2-dithiolate) and [Ni(cyclam)]2[Fe2(cbdt)4]2·4DMF (5), were prepared and characterised by X-ray diffraction and magnetisation measurements. The crystal structures of 1-4 were determined by single-crystal X-ray diffraction, which revealed that the cyano groups from dithiolene complexes fail to coordinate the metal ions in the cyclam units. Instead, they are coordinated by solvent molecules or by dithiolene S atoms and cyclam N-H groups, which participate in hydrogen bonds to the nitrile and sulfur moieties in the anions. [PUBLICATION ABSTRACT]
Author Belo, Dulce
Pereira, Laura C. J.
Fourmigué, Marc
Almeida, Manuel
Cerdeira, Ana C.
Simão, Dulce
Coutinho, Joana T.
Rabaça, Sandra
Jeannin, Olivier
Henriques, Rui T.
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  givenname: Dulce
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  givenname: Sandra
  surname: Rabaça
  fullname: Rabaça, Sandra
  organization: ITN/IST, Instituto Superior Técnico/CFMCUL, E.N. 10, 2686-953 Sacavém, Portugal, http://www.itn.pt/sec/qui/qfes/uk_qfes_index.htm
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  organization: Centro de Química Estrutural, Instituto Superior Técnico, Av. Rovisco Pais, 1049-001 Lisboa, Portugal
– sequence: 7
  givenname: Rui T.
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  fullname: Henriques, Rui T.
  organization: Instituto de Telecomunicações, Polo de Lisboa Av. Rovisco Pais, 1049-001 Lisboa, Portugal
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  surname: Jeannin
  fullname: Jeannin, Olivier
  organization: Institut des Sciences Chimiques de Rennes, Université Rennes 1 & CNRS, Campus de Beaulieu, 35042 Rennes, France
– sequence: 9
  givenname: Marc
  surname: Fourmigué
  fullname: Fourmigué, Marc
  organization: Institut des Sciences Chimiques de Rennes, Université Rennes 1 & CNRS, Campus de Beaulieu, 35042 Rennes, France
– sequence: 10
  givenname: Manuel
  surname: Almeida
  fullname: Almeida, Manuel
  email: malmeida@ctn.ist.utl.pt
  organization: ITN/IST, Instituto Superior Técnico/CFMCUL, E.N. 10, 2686-953 Sacavém, Portugal, http://www.itn.pt/sec/qui/qfes/uk_qfes_index.htm
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Issue 26
Keywords Macrocyclic ligands
Dithiolene ligands
Coordination modes
Heterometallic complexes
Magnetic properties
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Snippet Five charge‐transfer salts based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni,...
Five charge‐transfer salts based on the combination of anionic Fe III and Cu II bis(dithiolene) complexes containing nitrile groups with [M(cyclam)] 2+ (M =...
Five charge-transfer salts based on the combination of anionic FeIII and CuII bis(dithiolene) complexes containing nitrile groups with [M(cyclam)]2+ (M = Ni,...
Five charge-transfer salts based on the combination of anionic Fe super(III) and Cu super(II) bis(dithiolene) complexes containing nitrile groups with...
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SubjectTerms Atomic structure
Cations
Chemical Sciences
Coordination modes
Crystal structure
Dithiolene ligands
Heterometallic complexes
Hydrogen bonds
Macrocyclic ligands
Magnetic properties
Nickel
Nitriles
Organic chemistry
Solvents
X ray diffraction
Title Heterodimetallic Structures Based on Cyano-Substituted Bis(dithiolene) Complexes and Ni and Cu Cyclam Cations
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