Synthesis and properties of naphthalene trimers linked by 1,3,4-oxadiazole spacers

Tetrahedron Letters

Volumn 49, Issue 40, 2008, Pages 5816-5819

  Ono, Katsuhiko ^a   Ito, Hiroki ^a   Nakashima, Akihiro ^a   Uemoto, Mariko ^a   Tomura, Masaaki ^b   Saito, Katsuhiro ^a  

^a NAGOYA INSTITUTE OF TECHNOLOGY   (Japan)

^b INSTITUTE FOR MOLECULAR SCIENCE   (Japan)

Author keywords

Conjugation; Molecular aggregation; Naphthalene; Oxadiazole; Regioisomer

Indexed keywords

1,3,4 OXADIAZOLE DERIVATIVE; 2,5 DI 2 NAPHTHYL 1,3,4 OXADIAZOLE; DI 2 NAPHTHYLOXADIAZOLE DERIVATIVE; NAPHTHALENE DERIVATIVE; OXADIAZOLE DERIVATIVE;

ARTICLE; CALCULATION; CHEMICAL STRUCTURE; CONJUGATION; CROSS LINKING; DIFFERENTIAL SCANNING CALORIMETRY; MELTING POINT; QUANTUM YIELD; X RAY CRYSTALLOGRAPHY;

EID: 49849099496     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.07.122     Document Type: Article

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16. 6): δ 4.60 (br s, 4H), 7.96 (d, J = 8.9 Hz, 2H), 8.08 (d, J = 8.9 Hz, 2H), 8.46 (s, 2H), 10.01 (br s, 2H).
17. 6): δ 7.66-7.68 (m, 4H), 8.05-8.13 (m, 10H), 8.26 (d, J = 8.5 Hz, 2H), 8.61 (s, 2H), 8.67 (s, 2H), 10.80 (s, 2H), 10.85 (s, 2H).
18. 2: C, 79.06; H, 3.90; N, 10.85. Found: C, 78.97; H, 3.80; N, 10.86.
19. 2: C, 79.06; H, 3.90; N, 10.85. Found: C, 79.13; H, 3.81; N, 10.93.
20. -1 under nitrogen.
21. +.
22. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.
23. w = 0.1726, GOF = 1.128. CCDC 686869.