Ruthenium Stilbenyl and Diruthenium Distyrylethene Complexes: Aspects of Electron Delocalization and Electrocatalyzed Isomerization of the Z-Isomer

Regio- and stereoselective insertion of the terminal ethynyl functions of 4-ethynylstilbene, the E and Z isomers of 4,4'-bis(ethynylphenyl)ethene and a backbone-rigidified cyclohexenyl derivative of the Z. isomer into the Ru-H bond of the complex RuClH(CO)((PPr3)-Pr-i)(2) provides the correspon...

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Vydáno v:Journal of the American Chemical Society Ročník 134; číslo 40; s. 16671 - 16692
Hlavní autoři: Linseis, Michael, Zalis, Stanislav, Zabel, Manfred, Winter, Rainer F.
Médium: Journal Article
Jazyk:angličtina
Vydáno: WASHINGTON Amer Chemical Soc 10.10.2012
Témata:
Chemistry
Chemistry, Multidisciplinary
Physical Sciences
Science & Technology
VIBRATIONAL TIME-SCALE
CRYSTAL-STRUCTURE
MIXED-VALENCE STATE
AB-INITIO
RADICAL CATIONS
ABSORPTION-SPECTRA
CYCLIC VOLTAMMETRY
CHARGE-TRANSFER
RESONANCE RAMAN
CIS-TRANS-ISOMERIZATION
ISSN:0002-7863, 1520-5126, 1520-5126
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Abstract Regio- and stereoselective insertion of the terminal ethynyl functions of 4-ethynylstilbene, the E and Z isomers of 4,4'-bis(ethynylphenyl)ethene and a backbone-rigidified cyclohexenyl derivative of the Z. isomer into the Ru-H bond of the complex RuClH(CO)((PPr3)-Pr-i)(2) provides the corresponding vinyl ruthenium complexes, which have been characterized spectroscopically and by X-ray crystallography. Large red shifts of the UV/vis absorption bands evidence efficient incorporation of the vinyl metal subunit(s) into the conjugated pi-system. All complexes oxidize at low potentials. The various oxidized forms of all complexes were generated and characterized by UV/vis/NIR, IR and EPR spectroscopies. These studies indicated electrocatalytic Z -> E isomerization of the oxidized Z-distyrylethene complex Ru-Z2, which is prevented in its backbone-rigidified derivative Ru-Z2fix. The radical cations of the E and the configurationally stable cyclohexene-bridged Z-derivatives are spin-delocalized on the EPR time scale but charge-localized on the faster IR time scale. The degree of ground-state charge delocalization in the mixed-valent state has been quantified by the incremental shifts of the Ru-CO bands upon stepwise oxidation to the radical cations and the dications and was found to be remarkably large (19% and 9%) considering redox splittings Delta E-1/2 of just 49 or 74 mV. Quantum chemical studies with various levels of sophistication reproduce our experimental results including the electronic spectra of the neutral complexes and the intrinsically localized nature of the radical cations of the dinuclear complexes.
AbstractList Regio- and stereoselective insertion of the terminal ethynyl functions of 4-ethynylstilbene, the E and Z isomers of 4,4'-bis(ethynylphenyl)ethene and a backbone-rigidified cyclohexenyl derivative of the Z. isomer into the Ru-H bond of the complex RuClH(CO)((PPr3)-Pr-i)(2) provides the corresponding vinyl ruthenium complexes, which have been characterized spectroscopically and by X-ray crystallography. Large red shifts of the UV/vis absorption bands evidence efficient incorporation of the vinyl metal subunit(s) into the conjugated pi-system. All complexes oxidize at low potentials. The various oxidized forms of all complexes were generated and characterized by UV/vis/NIR, IR and EPR spectroscopies. These studies indicated electrocatalytic Z -> E isomerization of the oxidized Z-distyrylethene complex Ru-Z2, which is prevented in its backbone-rigidified derivative Ru-Z2fix. The radical cations of the E and the configurationally stable cyclohexene-bridged Z-derivatives are spin-delocalized on the EPR time scale but charge-localized on the faster IR time scale. The degree of ground-state charge delocalization in the mixed-valent state has been quantified by the incremental shifts of the Ru-CO bands upon stepwise oxidation to the radical cations and the dications and was found to be remarkably large (19% and 9%) considering redox splittings Delta E-1/2 of just 49 or 74 mV. Quantum chemical studies with various levels of sophistication reproduce our experimental results including the electronic spectra of the neutral complexes and the intrinsically localized nature of the radical cations of the dinuclear complexes.
Regio- and stereoselective insertion of the terminal ethynyl functions of 4-ethynylstilbene, the E and Z isomers of 4,4'-bis(ethynylphenyl)ethene and a backbone-rigidified cyclohexenyl derivative of the Z isomer into the Ru-H bond of the complex RuClH(CO)(P(i)Pr(3))(2) provides the corresponding vinyl ruthenium complexes, which have been characterized spectroscopically and by X-ray crystallography. Large red shifts of the UV/vis absorption bands evidence efficient incorporation of the vinyl metal subunit(s) into the conjugated π-system. All complexes oxidize at low potentials. The various oxidized forms of all complexes were generated and characterized by UV/vis/NIR, IR and EPR spectroscopies. These studies indicated electrocatalytic Z→E isomerization of the oxidized Z-distyrylethene complex Ru-Z2, which is prevented in its backbone-rigidified derivative Ru-Z2fix. The radical cations of the E and the configurationally stable cyclohexene-bridged Z-derivatives are spin-delocalized on the EPR time scale but charge-localized on the faster IR time scale. The degree of ground-state charge delocalization in the mixed-valent state has been quantified by the incremental shifts of the Ru-CO bands upon stepwise oxidation to the radical cations and the dications and was found to be remarkably large (19% and 9%) considering redox splittings ΔE(1/2) of just 49 or 74 mV. Quantum chemical studies with various levels of sophistication reproduce our experimental results including the electronic spectra of the neutral complexes and the intrinsically localized nature of the radical cations of the dinuclear complexes.
Regio- and stereoselective insertion of the terminal ethynyl functions of 4-ethynylstilbene, the E and Z isomers of 4,4'-bis(ethynylphenyl)ethene and a backbone-rigidified cyclohexenyl derivative of the Z isomer into the Ru-H bond of the complex RuClH(CO)(P(i)Pr(3))(2) provides the corresponding vinyl ruthenium complexes, which have been characterized spectroscopically and by X-ray crystallography. Large red shifts of the UV/vis absorption bands evidence efficient incorporation of the vinyl metal subunit(s) into the conjugated π-system. All complexes oxidize at low potentials. The various oxidized forms of all complexes were generated and characterized by UV/vis/NIR, IR and EPR spectroscopies. These studies indicated electrocatalytic Z→E isomerization of the oxidized Z-distyrylethene complex Ru-Z2, which is prevented in its backbone-rigidified derivative Ru-Z2fix. The radical cations of the E and the configurationally stable cyclohexene-bridged Z-derivatives are spin-delocalized on the EPR time scale but charge-localized on the faster IR time scale. The degree of ground-state charge delocalization in the mixed-valent state has been quantified by the incremental shifts of the Ru-CO bands upon stepwise oxidation to the radical cations and the dications and was found to be remarkably large (19% and 9%) considering redox splittings ΔE(1/2) of just 49 or 74 mV. Quantum chemical studies with various levels of sophistication reproduce our experimental results including the electronic spectra of the neutral complexes and the intrinsically localized nature of the radical cations of the dinuclear complexes.Regio- and stereoselective insertion of the terminal ethynyl functions of 4-ethynylstilbene, the E and Z isomers of 4,4'-bis(ethynylphenyl)ethene and a backbone-rigidified cyclohexenyl derivative of the Z isomer into the Ru-H bond of the complex RuClH(CO)(P(i)Pr(3))(2) provides the corresponding vinyl ruthenium complexes, which have been characterized spectroscopically and by X-ray crystallography. Large red shifts of the UV/vis absorption bands evidence efficient incorporation of the vinyl metal subunit(s) into the conjugated π-system. All complexes oxidize at low potentials. The various oxidized forms of all complexes were generated and characterized by UV/vis/NIR, IR and EPR spectroscopies. These studies indicated electrocatalytic Z→E isomerization of the oxidized Z-distyrylethene complex Ru-Z2, which is prevented in its backbone-rigidified derivative Ru-Z2fix. The radical cations of the E and the configurationally stable cyclohexene-bridged Z-derivatives are spin-delocalized on the EPR time scale but charge-localized on the faster IR time scale. The degree of ground-state charge delocalization in the mixed-valent state has been quantified by the incremental shifts of the Ru-CO bands upon stepwise oxidation to the radical cations and the dications and was found to be remarkably large (19% and 9%) considering redox splittings ΔE(1/2) of just 49 or 74 mV. Quantum chemical studies with various levels of sophistication reproduce our experimental results including the electronic spectra of the neutral complexes and the intrinsically localized nature of the radical cations of the dinuclear complexes.
Author Linseis, Michael
Winter, Rainer F.
Zalis, Stanislav
Zabel, Manfred
Author_xml – sequence: 1
  givenname: Michael
  orcidid: 0000-0003-0861-8537
  surname: Linseis
  fullname: Linseis, Michael
  organization: Univ Konstanz, Fachbereich Chem, D-78457 Constance, Germany
– sequence: 2
  givenname: Stanislav
  orcidid: 0000-0003-4345-3205
  surname: Zalis
  fullname: Zalis, Stanislav
  organization: Acad Sci Czech Republ, J Heyrovsky Inst Phys Chem Vvi, Prague, Czech Republic
– sequence: 3
  givenname: Manfred
  surname: Zabel
  fullname: Zabel, Manfred
  organization: Univ Regensburg, Inst Anorgan Chem, D-93040 Regensburg, Germany
– sequence: 4
  givenname: Rainer F.
  surname: Winter
  fullname: Winter, Rainer F.
  email: rainer.winter@uni-konstanz.de
  organization: Univ Konstanz, Fachbereich Chem, D-78457 Constance, Germany
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Issue 40
Keywords VIBRATIONAL TIME-SCALE
CRYSTAL-STRUCTURE
MIXED-VALENCE STATE
AB-INITIO
RADICAL CATIONS
ABSORPTION-SPECTRA
CYCLIC VOLTAMMETRY
CHARGE-TRANSFER
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  year: 2003
  ident: WOS:000181024000018
  article-title: Synthesis and characterization of bimetallic ruthenium complexes with (CH)6 and related bridges
  publication-title: ORGANOMETALLICS
  doi: 10.1021/om0207663
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Snippet Regio- and stereoselective insertion of the terminal ethynyl functions of 4-ethynylstilbene, the E and Z isomers of 4,4'-bis(ethynylphenyl)ethene and a...
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StartPage 16671
SubjectTerms Chemistry
Chemistry, Multidisciplinary
Physical Sciences
Science & Technology
Title Ruthenium Stilbenyl and Diruthenium Distyrylethene Complexes: Aspects of Electron Delocalization and Electrocatalyzed Isomerization of the Z-Isomer
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