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      Chromium Complexes with Oxido and Corrolato Ligands: Metal‐Based Redox Processes versus Ligand Non‐Innocence

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      https://www.riss.kr/link?id=O120653742

      • 저자
      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2018년

      • 작성언어

        -

      • Print ISSN

        0947-6539

      • Online ISSN

        1521-3765

      • 등재정보

        SCI;SCIE;SCOPUS

      • 자료형태

        학술저널

      • 수록면

        12613-12622   [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]

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        • 전북대학교 중앙도서관  
        • 성균관대학교 중앙학술정보관  
        • 부산대학교 중앙도서관  
        • 전남대학교 중앙도서관  
        • 제주대학교 중앙도서관  
        • 중앙대학교 서울캠퍼스 중앙도서관  
        • 인천대학교 학산도서관  
        • 숙명여자대학교 중앙도서관  
        • 서강대학교 로욜라중앙도서관  
        • 계명대학교 동산도서관  
        • 충남대학교 중앙도서관  
        • 한양대학교 백남학술정보관  
        • 이화여자대학교 중앙도서관  
        • 고려대학교 도서관  
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      다국어 초록 (Multilingual Abstract)

      Metal‐ versus ligand‐centered redox processes and the effects of substituents on the ligands on the spectroscopic properties of the metal complexes are at the heart of research on metal complexes with non‐innocent ligands. This work presents three examples of chromium complexes that contain both oxido and corrolato ligands, with the substituents on the corrolato ligands being different in the three cases. Combined X‐ray crystallographic, electrochemical, UV/Vis/NIR/EPR spectroelectrochemical, and EXAFS/XANES measurements, together with DFT calculations, have been used to probe the complexes in three different redox forms. This combined approach makes it possible to address questions related to chromium‐ versus corrolato‐centered redox processes, and the accessibility (or not) of CrIV, CrV, and CrVI in these complexes, as well as their spin states. To the best of our knowledge, these are the first EXAFS/XANES investigations on Cr‐corrolato complexes in different redox forms, and hence these data should set benchmarks for future investigations on such complexes by this method.
      Metal‐ or ligand‐centered redox? UV/Vis/NIR/EPR spectroelectrochemical and XANES measurements, together with DFT calculations, have been applied to address the issue of chromium‐ versus corrolato‐centered redox processes, and the accessibility (or not) of CrIV, CrV, and CrVI in these complexes, as well as their spin states.
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      Metal‐ versus ligand‐centered redox processes and the effects of substituents on the ligands on the spectroscopic properties of the metal complexes are at the heart of research on metal complexes with non‐innocent ligands. This work presents thr...

      Metal‐ versus ligand‐centered redox processes and the effects of substituents on the ligands on the spectroscopic properties of the metal complexes are at the heart of research on metal complexes with non‐innocent ligands. This work presents three examples of chromium complexes that contain both oxido and corrolato ligands, with the substituents on the corrolato ligands being different in the three cases. Combined X‐ray crystallographic, electrochemical, UV/Vis/NIR/EPR spectroelectrochemical, and EXAFS/XANES measurements, together with DFT calculations, have been used to probe the complexes in three different redox forms. This combined approach makes it possible to address questions related to chromium‐ versus corrolato‐centered redox processes, and the accessibility (or not) of CrIV, CrV, and CrVI in these complexes, as well as their spin states. To the best of our knowledge, these are the first EXAFS/XANES investigations on Cr‐corrolato complexes in different redox forms, and hence these data should set benchmarks for future investigations on such complexes by this method.
      Metal‐ or ligand‐centered redox? UV/Vis/NIR/EPR spectroelectrochemical and XANES measurements, together with DFT calculations, have been applied to address the issue of chromium‐ versus corrolato‐centered redox processes, and the accessibility (or not) of CrIV, CrV, and CrVI in these complexes, as well as their spin states.

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