A new dyad based on C60 and a conjugated dimethylaniline-substituted dithienylethylene donor

Journal of Organic Chemistry

Volumn 64, Issue 13, 1999, Pages 4884-4886

  Liu, Sheng Gao ^a   Shu, Lianhe ^a   Rivera, José ^b   Liu, Haiying ^a   Raimundo, Jean Manuel ^c   Roncali, Jean ^c   Gorgues, Alain ^c   Echegoyen, Luis ^a  

^a Department of Biology   (United States)

^b Pontifical Catholic University of Puerto Rico   (Puerto Rico)

^c UNIVERSITÉ D'ANGERS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANILINE DERIVATIVE; DIMETHYLANILINE; DITHIENYLETHYLENE DERIVATIVE; ETHYLENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; ELECTRON TRANSPORT; POTENTIOMETRY; SYNTHESIS;

EID: 0033603615     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990287m     Document Type: Article

References (31)

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2. 60-based donor-acceptor molecular assemblies: (a) Martin, N.; Sánchez, L.; Illescas, B.; Pérez, I. Chem. Rev. 1998, 98, 2527-2547. (b) Prato, M.; Maggini, M. Acc. Chem. Res. 1998, 31, 519-530.
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26. 3c was synthesized by the methodology developed by Jen et al. with a slight modification; see ref 14a.
27. 3 1/1, one carbon for each piece of data unless otherwise indicated in parentheses) 40.27, 70.01, 79.14, 68.60, 125.31, 126.55 (2 C), 126.60 (2 C), 127.85 (2 C), 128.21, 128.97, 135.58, 135.81, 136.61, 136.97, 139.59, 139.87, 140.14, 140.67, 141.55, 141.62, 141.86, 141.92, 142.00, 142.07, 142.11 (2 C), 142.14, 142.23, 142.55 (2 C), 142.65, 142.94, 143.11, 144.31, 144.60, 144.66, 145.10, 145.19 (2 C), 145.21, 145.28, 145.32, 145.42, 145.53, 145.57, 145.71, 145.88 (2 C), 146.03, 146.06, 146.10, 146.15, 146.19, 146.22 (2 C), 146.30, 146.78, 147.25 (2 C), 153.00, 153.07, 153.75, 155.77.
28. 60 and the donor moiety listed as follows (one carbon for each piece of data unless otherwise indicated in parentheses): 112.45 (2 C), 117.59, 120.67, 122.28, 125.23, 125.29, 125.58, 127.53, 127.64 (2 C), 128.26, 128.59, 129.00, 129.37, 135.56, 135.78, 136.66, 137.03, 139.43, 139.79, 139.87, 139.94, 140.15 (2 C), 141.59, 141.62, 141.90 (2 C), 141.95, 142.01, 142.05, 142.10 (2 C), 142.15, 142.24, 142.55 (2 C), 142.66, 142.94, 143.12, 143.61, 143.98, 144.30, 144.33, 144.65 (2 C), 145.12, 145.17, 145.21 (2 C), 145.26, 145.34, 145.38, 145.41, 145.53, 145.60, 145.72, 145.88 (2 C), 146.03, 146.08, 146.12, 146.16, 146.19, 146.23, 146.26, 146.30, 146.77, 147.23, 147.26, 149.80, 152.91, 153.00, 153.72, 155.71 ppm.
29. Chou, S. S. P.; Sun, D. J.; Huang, J. Y.; Yang, P. K.; Lin, H. C. Tetrahedron Lett. 1996, 37, 7279-7282.
30. Arias, F.; Echegoyen, L.; Wilson, S. R.; Lu, Q.; Lu, Q. Y. J. Am. Chem. Soc. 1995, 117, 1422-1427.
31. 60 derivatives.