Di([5]trovacenyl)ethyne, Di([5]trovacenyl)butadiyne, and Di-1,4-([5]trovacenylethynyl)benzene:  Electrocommunication and Magnetocommunication Mediated by C⋮C, C⋮CC⋮C and C⋮CC6H4C⋮C Spacers

The synthesis of dinuclear derivatives of trovacene (η7-C7H7)V(η5-C5H5) (1 • ) is reported, in which ethynyl (6 • • ), butadiynyl (7 • • ), and 1,4-di(ethynyl)phenyl (8 • • ) groups serve as spacers between paramagnetic (S = 1/2) [5]trovacenyl units. The mononuclear precursors [5]trovacenylcarbaldeh...

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Veröffentlicht in:Inorganic chemistry 2005-02, Vol.44 (4), p.955-963
Hauptverfasser: Elschenbroich, Christoph, Plackmeyer, Jörn, Nowotny, Mathias, Harms, Klaus, Pebler, Jürgen, Burghaus, Olaf
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container_issue 4
container_start_page 955
container_title Inorganic chemistry
container_volume 44
creator Elschenbroich, Christoph
Plackmeyer, Jörn
Nowotny, Mathias
Harms, Klaus
Pebler, Jürgen
Burghaus, Olaf
description The synthesis of dinuclear derivatives of trovacene (η7-C7H7)V(η5-C5H5) (1 • ) is reported, in which ethynyl (6 • • ), butadiynyl (7 • • ), and 1,4-di(ethynyl)phenyl (8 • • ) groups serve as spacers between paramagnetic (S = 1/2) [5]trovacenyl units. The mononuclear precursors [5]trovacenylcarbaldehyde (2 • ) and [5]trovacenylacetylene (4 • ) are also described. Structural characterization by X-ray diffraction has been performed for 4 • , 6 • • , 7 • • , and 8 • • . Electronic communication as gleaned from cyclic voltammetry only manifests itself in the reduction processes where redox splitting δE 1/2(0/1−, 1−/2−) is resolved for 6 • • (δE 1/2 = 150 mV) and indicated for 7 • • (δE1/2 ≲ 80 mV). Magnetocommunication leads to exchange coupling of the two electron spins which reside in vanadium centered orbitals. The values J EPR(6 • • ) = (−)0.92, J EPR(7 • • ) = (−)0.56, and J EPR(8 • • ) = (−)0.005 cm-1 are derived from the 51V hyperfine patterns. Accordingly, attenuation of exchange interaction by oligoalkyne spacers is weak, corresponding to a factor of 0.6 only per added C⋮C unit. In the determination of very weak long distance exchange interactions, EPR excels because of the range 5 × 10-4 ≲ J ≲ 1.5 cm-1 accessible in the case of 51V as a reporting magnetic nucleus and because competing intermolecular exchange is quenched in dilute fluid solution. This is demonstrated by the value J χ(7 • • ) = −3.84 cm-1 obtained from a magnetic susceptibility study, which exceeds J EPR(7 • • ) by a factor of 7. The small magnitude of spin exchange interaction between trovacene units reflects the fact that the spin bearing V3d z 2 orbital is virtually orthogonal to the π-perimeter ligand orbitals and weakly overlapping only with the a1g(σ) ring orbitals, creating two bottlenecks for spin-exchange in the spacer-containing ditrovacenes.
doi_str_mv 10.1021/ic040090z
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The mononuclear precursors [5]trovacenylcarbaldehyde (2 • ) and [5]trovacenylacetylene (4 • ) are also described. Structural characterization by X-ray diffraction has been performed for 4 • , 6 • • , 7 • • , and 8 • • . Electronic communication as gleaned from cyclic voltammetry only manifests itself in the reduction processes where redox splitting δE 1/2(0/1−, 1−/2−) is resolved for 6 • • (δE 1/2 = 150 mV) and indicated for 7 • • (δE1/2 ≲ 80 mV). Magnetocommunication leads to exchange coupling of the two electron spins which reside in vanadium centered orbitals. The values J EPR(6 • • ) = (−)0.92, J EPR(7 • • ) = (−)0.56, and J EPR(8 • • ) = (−)0.005 cm-1 are derived from the 51V hyperfine patterns. Accordingly, attenuation of exchange interaction by oligoalkyne spacers is weak, corresponding to a factor of 0.6 only per added C⋮C unit. 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Chem</addtitle><description>The synthesis of dinuclear derivatives of trovacene (η7-C7H7)V(η5-C5H5) (1 • ) is reported, in which ethynyl (6 • • ), butadiynyl (7 • • ), and 1,4-di(ethynyl)phenyl (8 • • ) groups serve as spacers between paramagnetic (S = 1/2) [5]trovacenyl units. The mononuclear precursors [5]trovacenylcarbaldehyde (2 • ) and [5]trovacenylacetylene (4 • ) are also described. Structural characterization by X-ray diffraction has been performed for 4 • , 6 • • , 7 • • , and 8 • • . Electronic communication as gleaned from cyclic voltammetry only manifests itself in the reduction processes where redox splitting δE 1/2(0/1−, 1−/2−) is resolved for 6 • • (δE 1/2 = 150 mV) and indicated for 7 • • (δE1/2 ≲ 80 mV). Magnetocommunication leads to exchange coupling of the two electron spins which reside in vanadium centered orbitals. The values J EPR(6 • • ) = (−)0.92, J EPR(7 • • ) = (−)0.56, and J EPR(8 • • ) = (−)0.005 cm-1 are derived from the 51V hyperfine patterns. Accordingly, attenuation of exchange interaction by oligoalkyne spacers is weak, corresponding to a factor of 0.6 only per added C⋮C unit. In the determination of very weak long distance exchange interactions, EPR excels because of the range 5 × 10-4 ≲ J ≲ 1.5 cm-1 accessible in the case of 51V as a reporting magnetic nucleus and because competing intermolecular exchange is quenched in dilute fluid solution. This is demonstrated by the value J χ(7 • • ) = −3.84 cm-1 obtained from a magnetic susceptibility study, which exceeds J EPR(7 • • ) by a factor of 7. The small magnitude of spin exchange interaction between trovacene units reflects the fact that the spin bearing V3d z 2 orbital is virtually orthogonal to the π-perimeter ligand orbitals and weakly overlapping only with the a1g(σ) ring orbitals, creating two bottlenecks for spin-exchange in the spacer-containing ditrovacenes.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNplkc1Kw0AUhQdRsFYXvkE2gkKjdyaTNHEnsVqhxYUKgki4mbnRlHYiSSq0K7fiA_gWrn2euvcZTOMPVVdn5n5nzh04jG1y2OUg-F6qQAIEMF1iDe4KsF0Ol8usAVCduecFq2ytKAZQeRzpNdjbYbp95V6XeXaPisxkuEPl7cRQy_oH4nGJOq0ZGl1xm7ek_dtUP557yUzJ0P7s4dHqDElVDpWNRmOTKizTzNQJfbwxVP4BfdIplqSteGK9P7-Gs6eXsNLW4uVb65TFudeVi_jsrvpVXqyzlQSHBW18aZNdHHXOw67dOz0-CQ96NnLfLW3BXUTpIHCJJGPh-4o4JG0MpCu0L2IU6HgQCDdxBGjw234SkA40-ULFiec02dZnLqoiGmTj3FTbIg7RvJnopxnnA9pklAc</recordid><startdate>20050221</startdate><enddate>20050221</enddate><creator>Elschenbroich, Christoph</creator><creator>Plackmeyer, Jörn</creator><creator>Nowotny, Mathias</creator><creator>Harms, Klaus</creator><creator>Pebler, Jürgen</creator><creator>Burghaus, Olaf</creator><general>American Chemical Society</general><scope/></search><sort><creationdate>20050221</creationdate><title>Di([5]trovacenyl)ethyne, Di([5]trovacenyl)butadiyne, and Di-1,4-([5]trovacenylethynyl)benzene:  Electrocommunication and Magnetocommunication Mediated by C⋮C, C⋮CC⋮C and C⋮CC6H4C⋮C Spacers</title><author>Elschenbroich, Christoph ; Plackmeyer, Jörn ; Nowotny, Mathias ; Harms, Klaus ; Pebler, Jürgen ; Burghaus, Olaf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a185t-215aa43a014ae4b288ce10f7a9452d82ba2a360925f320d0878f9ed9de82cbf63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elschenbroich, Christoph</creatorcontrib><creatorcontrib>Plackmeyer, Jörn</creatorcontrib><creatorcontrib>Nowotny, Mathias</creatorcontrib><creatorcontrib>Harms, Klaus</creatorcontrib><creatorcontrib>Pebler, Jürgen</creatorcontrib><creatorcontrib>Burghaus, Olaf</creatorcontrib><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elschenbroich, Christoph</au><au>Plackmeyer, Jörn</au><au>Nowotny, Mathias</au><au>Harms, Klaus</au><au>Pebler, Jürgen</au><au>Burghaus, Olaf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Di([5]trovacenyl)ethyne, Di([5]trovacenyl)butadiyne, and Di-1,4-([5]trovacenylethynyl)benzene:  Electrocommunication and Magnetocommunication Mediated by C⋮C, C⋮CC⋮C and C⋮CC6H4C⋮C Spacers</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2005-02-21</date><risdate>2005</risdate><volume>44</volume><issue>4</issue><spage>955</spage><epage>963</epage><pages>955-963</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>The synthesis of dinuclear derivatives of trovacene (η7-C7H7)V(η5-C5H5) (1 • ) is reported, in which ethynyl (6 • • ), butadiynyl (7 • • ), and 1,4-di(ethynyl)phenyl (8 • • ) groups serve as spacers between paramagnetic (S = 1/2) [5]trovacenyl units. The mononuclear precursors [5]trovacenylcarbaldehyde (2 • ) and [5]trovacenylacetylene (4 • ) are also described. Structural characterization by X-ray diffraction has been performed for 4 • , 6 • • , 7 • • , and 8 • • . Electronic communication as gleaned from cyclic voltammetry only manifests itself in the reduction processes where redox splitting δE 1/2(0/1−, 1−/2−) is resolved for 6 • • (δE 1/2 = 150 mV) and indicated for 7 • • (δE1/2 ≲ 80 mV). Magnetocommunication leads to exchange coupling of the two electron spins which reside in vanadium centered orbitals. The values J EPR(6 • • ) = (−)0.92, J EPR(7 • • ) = (−)0.56, and J EPR(8 • • ) = (−)0.005 cm-1 are derived from the 51V hyperfine patterns. Accordingly, attenuation of exchange interaction by oligoalkyne spacers is weak, corresponding to a factor of 0.6 only per added C⋮C unit. In the determination of very weak long distance exchange interactions, EPR excels because of the range 5 × 10-4 ≲ J ≲ 1.5 cm-1 accessible in the case of 51V as a reporting magnetic nucleus and because competing intermolecular exchange is quenched in dilute fluid solution. This is demonstrated by the value J χ(7 • • ) = −3.84 cm-1 obtained from a magnetic susceptibility study, which exceeds J EPR(7 • • ) by a factor of 7. The small magnitude of spin exchange interaction between trovacene units reflects the fact that the spin bearing V3d z 2 orbital is virtually orthogonal to the π-perimeter ligand orbitals and weakly overlapping only with the a1g(σ) ring orbitals, creating two bottlenecks for spin-exchange in the spacer-containing ditrovacenes.</abstract><pub>American Chemical Society</pub><doi>10.1021/ic040090z</doi><tpages>9</tpages></addata></record>
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title Di([5]trovacenyl)ethyne, Di([5]trovacenyl)butadiyne, and Di-1,4-([5]trovacenylethynyl)benzene:  Electrocommunication and Magnetocommunication Mediated by C⋮C, C⋮CC⋮C and C⋮CC6H4C⋮C Spacers
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