Synthesis and coordination studies of new mono- and di-hydroxy functionalized 4,4'-dialkenyl-2,2'-bipyridines

Tetrahedron Letters

Volumn 39, Issue 38, 1998, Pages 6869-6872

  Le Bouder, Thomas ^a   Massiot, Philippe ^a   Le Bozec, Hubert ^a  

^a UMR 6509 Organometalliques et Catalyse Chimie et Electrochimie Moleculaires   (France)

Author keywords

[No Author keywords available]

Indexed keywords

2,2' BIPYRIDINE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY;

EID: 0032541733     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0040-4039(98)01499-3     Document Type: Article

References (16)

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14. 3) δ 8.59 (δ, J = 4.8 Hz, 1H), 8.57 (d, J = 4.8 Hz, 1H), 8.45 (s, 2H), 7.41 (d, J = 8 Hz, 4H), 7.37 (d, J = 16.4 Hz, 2H), 7.31 (d, J = 4.6 Hz, 4H), 6.90 (d, J = 16.1 Hz, 1H) 6.87 (d, J = 16.4 Hz, 1H), 6.69 (d, J = 8 Hz, 2H) 6.65 (d, J = 8.5 Hz, 2H), 3.89 (t, J = 4.5 Hz, 4H), 3.63 (t, J = 4.5 Hz, 4H), 3.88 (q, J = 7 Hz, 4H), 1.17 (t, J = 7 Hz, 6H).
15. 15. Sullivan, B. P.; Salmon, D. J.; Meyer, T. J. Inorg. Chem., 1978, 17, 3334-3341.
16. 2) δ 8.40 (s, 6H), 7.58-7.32 (m, 30H), 7.00 (d, J = 16 Hz, 1H), 6.94 (d, J = 16 Hz, 5H), 6.73 (d, J = 8.8 Hz, 2H), 6.67 (d, J = 8.8 Hz, 10H), 3.84 (t, J = 4.6 Hz, 4H), 3.62 (t, J = 4.6 Hz, 4H), 3.44-3.34 (m, 20H), 1.16 (t, J = 7.0 Hz, 30H).