Hexaphenylethane Derivatives Exhibiting Novel Electrochromic Behavior

Angewandte Chemie (International Edition in English)

Volumn 36, Issue 12, 1997, Pages 1329-1331

  Suzuki, Takanori ^a   Nishida, Jun Ich ^a   Tsuji, Takashi ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

Carbocations; Dyes; Electrochemistry; Redox chemistry

Indexed keywords

EID: 0030741419     PISSN: 05700833     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.199713291     Document Type: Article

References (10)

1. G. Wittig, H. Petri, Justus Liebigs Ann. Chem. 1933, 505, 17.
2. W. D. Hounshell, D. A. Dougherty, J. P. Hummel, K. Mislow, J. Am. Chem. Soc. 1977, 99, 1916.
3. P. Maslak, J. N. Narvaez, T. M. Vallombroso, Jr., J. Am. Chem. Soc., 1995 117, 12373; P. Maslak, W. H. Chapman, Jr., T. M. Vallombroso, Jr., B. A. Watson, ibid. 1995, 117, 12380.
4. P. Maslak, J. N. Narvaez, T. M. Vallombroso, Jr., J. Am. Chem. Soc., 1995 117, 12373; P. Maslak, W. H. Chapman, Jr., T. M. Vallombroso, Jr., B. A. Watson, ibid. 1995, 117, 12380.
5. G. Kratt, H. -D. Beckhaus, C. Rüchardt, Chem. Ber. 1984, 117, 1748.
6. G. Wittig, W. Herwig, Chem. Ber. 1954, 87, 1511.
7. Similar potential separation was also observed in 1.3-dimethylenecyclobutanes or bicyclic trichalcogenides which undergo structural change accompanied with transannular bonding upon two-electron oxidation: M Horner, S. Hünig, J. Am. Chem. Soc. 1977, 99, 6122; H. Fujihara, H. Mima, T. Erata, N. Furukawa, ibid. 1992, 114, 3117. Linkage isomerism in the transition metal complexes also leads to molecular hysteresis of this kind: M. Sano, H. Taube, ibid. 1991, 113, 2327; A. Livoreil, C. O. Dietrich-Buchecker, J. -P. Sauvage, ibid. 1994, 116, 9399.
8. Similar potential separation was also observed in 1.3-dimethylenecyclobutanes or bicyclic trichalcogenides which undergo structural change accompanied with transannular bonding upon two-electron oxidation: M Horner, S. Hünig, J. Am. Chem. Soc. 1977, 99, 6122; H. Fujihara, H. Mima, T. Erata, N. Furukawa, ibid. 1992, 114, 3117. Linkage isomerism in the transition metal complexes also leads to molecular hysteresis of this kind: M. Sano, H. Taube, ibid. 1991, 113, 2327; A. Livoreil, C. O. Dietrich-Buchecker, J. -P. Sauvage, ibid. 1994, 116, 9399.
9. Similar potential separation was also observed in 1.3-dimethylenecyclobutanes or bicyclic trichalcogenides which undergo structural change accompanied with transannular bonding upon two-electron oxidation: M Horner, S. Hünig, J. Am. Chem. Soc. 1977, 99, 6122; H. Fujihara, H. Mima, T. Erata, N. Furukawa, ibid. 1992, 114, 3117. Linkage isomerism in the transition metal complexes also leads to molecular hysteresis of this kind: M. Sano, H. Taube, ibid. 1991, 113, 2327; A. Livoreil, C. O. Dietrich-Buchecker, J. -P. Sauvage, ibid. 1994, 116, 9399.
10. Similar potential separation was also observed in 1.3-dimethylenecyclobutanes or bicyclic trichalcogenides which undergo structural change accompanied with transannular bonding upon two-electron oxidation: M Horner, S. Hünig, J. Am. Chem. Soc. 1977, 99, 6122; H. Fujihara, H. Mima, T. Erata, N. Furukawa, ibid. 1992, 114, 3117. Linkage isomerism in the transition metal complexes also leads to molecular hysteresis of this kind: M. Sano, H. Taube, ibid. 1991, 113, 2327; A. Livoreil, C. O. Dietrich-Buchecker, J. -P. Sauvage, ibid. 1994, 116, 9399.