Spiroconjugation in Spirodicorrolato-Dinickel(II)

Chemistry - A European Journal

Volumn 9, Issue 22, 2003, Pages 5636-5642

  Hohlneicher, Georg ^a   Bremm, Dominik ^a   Wytko, Jennifer ^b   Bley Escrich, Jordi ^b   Gisselbrecht, Jean Paul ^b   Gross, Maurice ^b   Michels, Martin ^a   Lex, Johann ^a   Vogel, Emanuel ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

^b CNRS   (France)

Author keywords

Electrochemistry; Electron spectroscopy; Porphyrinoids; Spiro compounds; Spiroconjugation

Indexed keywords

ABSORPTION; COMPLEXATION; ELECTRONIC STRUCTURE; NICKEL COMPOUNDS; REDOX REACTIONS; SPECTRUM ANALYSIS;

SPIROCONJUGATION;

ELECTROCHEMISTRY;

METAL COMPLEX; NICKEL COMPLEX;

ABSORPTION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; COMPARATIVE STUDY; COMPLEX FORMATION; CONJUGATION; ELECTROCHEMICAL ANALYSIS; ELECTROCHEMISTRY; MATHEMATICAL ANALYSIS; OXIDATION REDUCTION REACTION;

EID: 0346458661     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200305094     Document Type: Article

References (45)

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5. Isocorrole is analogous to the hypothetic porphyrin tautomer isoporphyrin (H. Scheer, J. J. Katz in Porphyrins and Metalloporphyrins (Ed.: K. M. Smith), Elsevier, Amsterdam, 1975, p. 449). In one of our previous publications the name isocorrole was given to the corrole constitutional isomer corrole(2.0.1.0) (E. Vogel, B. Binsack, Y. Hellwig, C. Erben, A. Heger, J. Lex, Y.-D. Wu, Angew. Chem. 1997, 109, 2725-2728; Angew. Chem. Int. Ed. Engl. 1997, 36, 2612-2615). To avoid confusion it is suggested to denote corrole(2.0.1.0) by the trivial name corrolene. In light of this overlap, 1 might better be called spirodiisocorrole.
6. Isocorrole is analogous to the hypothetic porphyrin tautomer isoporphyrin (H. Scheer, J. J. Katz in Porphyrins and Metalloporphyrins (Ed.: K. M. Smith), Elsevier, Amsterdam, 1975, p. 449). In one of our previous publications the name isocorrole was given to the corrole constitutional isomer corrole(2.0.1.0) (E. Vogel, B. Binsack, Y. Hellwig, C. Erben, A. Heger, J. Lex, Y.-D. Wu, Angew. Chem. 1997, 109, 2725-2728; Angew. Chem. Int. Ed. Engl. 1997, 36, 2612-2615). To avoid confusion it is suggested to denote corrole(2.0.1.0) by the trivial name corrolene. In light of this overlap, 1 might better be called spirodiisocorrole.
7. Isocorrole is analogous to the hypothetic porphyrin tautomer isoporphyrin (H. Scheer, J. J. Katz in Porphyrins and Metalloporphyrins (Ed.: K. M. Smith), Elsevier, Amsterdam, 1975, p. 449). In one of our previous publications the name isocorrole was given to the corrole constitutional isomer corrole(2.0.1.0) (E. Vogel, B. Binsack, Y. Hellwig, C. Erben, A. Heger, J. Lex, Y.-D. Wu, Angew. Chem. 1997, 109, 2725-2728; Angew. Chem. Int. Ed. Engl. 1997, 36, 2612-2615). To avoid confusion it is suggested to denote corrole(2.0.1.0) by the trivial name corrolene. In light of this overlap, 1 might better be called spirodiisocorrole.
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