journal article·1992-11

Synthesis of unsymmetrical biaryls via low‐coordination palladium species

Sophie Gervat, Eric Léonel, Jean‐Yves Barraud, Victorin Ratovelomanana

Advanced Materials· Volume 4· Issue 11
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Abstract

The biaryl unit is a fundamental feature of a large number of nonlinear optical materials and liquid crystals. Unsymmetrical biaryls (see figure) have been shown to be of particular interest, exhibiting amongst other things a high electro‐optic coefficient. The synthesis of the new unsymmetrical biaryls involves the palladium‐complexcatalyzed coupling of an organometallic derivative with an aromatic halide. magnified image
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Research context

OpenAlex topics: Catalytic Cross-Coupling Reactions · Axial and Atropisomeric Chirality Synthesis · Catalytic C–H Functionalization Methods

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References (33)

Show source-provided references
1. 10.1002/anie.19840690110.1002/anie.198406901 ↗
2. Chemla D. S. · 1987
3. Prasad C. N. · 1991
4. Singer K. D. · 1991
5. J. F.Fauvarque V.Ratovelomanana A.Jutand C.Amatore French Patent Demande Alcatel N.V. 9109180 1989.
6. C.Amatore J. F.Fauvarque A.Jutand S.Negri French Patent Demande: Alcatel N.V. 9109180 1989.
7. 10.1016/0301-0104(91)90062-X10.1016/0301-0104(91)90062-X ↗
8. R.Hytel G. F.Lipscomb M.Stiller J. I.Thackara A. J.Ticknor Nonlinear Optical Effects in Organic Polymers(Eds.:J.Messieret al.) 1989 p.277.10.1007/978-94-009-2295-2_22 ↗
9. 10.1007/BF0218921410.1007/BF02189214 ↗
10. J. Y.Barraud S.Gervat J. F.Fauvarque V.Ratovelomanana French Patent Demande: Alcatel N.V. 9109180 1991.
11. Tamao A. K. · 1986
12. Norton R. F. · 1987
13. Heck R. F. · 1985
14. S.Sibille V.Ratovelomanana J.Périchon J. Chem. Soc. Chem. Commun.1992 283.10.1039/C39920000283 ↗
15. 10.1021/jo00430a04110.1021/jo00430a041 ↗
16. 10.1016/B978-0-08-029217-5.50027-910.1016/B978-0-08-029217-5.50027-9 ↗
17. 10.1021/ja00252a02910.1021/ja00252a029 ↗
18. 10.1016/0022-328X(83)85077-310.1016/0022-328X(83)85077-3 ↗
19. 10.1021/ja00025a02510.1021/ja00025a025 ↗
20. Y.Hatanaka T.Hiyama Synlett1991 845.10.1055/s-1991-20899 ↗
21. 10.1080/0039791810806361810.1080/00397918108063618 ↗
22. 10.1021/jo00200a04510.1021/jo00200a045 ↗
23. (c)W. A.Cristofoli B. A.Keay Tetrahedron Lett.1991 5880.
24. 10.1246/bcsj.62.389610.1246/bcsj.62.3896 ↗
25. 10.1021/jo01351a09210.1021/jo01351a092 ↗
26. 10.1021/jo01351a09310.1021/jo01351a093 ↗
27. 10.1021/ja00249a07010.1021/ja00249a070 ↗
28. 10.1246/bcsj.61.300810.1246/bcsj.61.3008 ↗
29. Stifle J. K. · Argew. Chem. Int. Ed. Engl. · 1983 · 25 · 551
30. E.Negishi T.Takahashi K.Akiyoshi J. Chem. Soc. Chem. Commun.1986 1338.10.1039/C39860001338 ↗
31. Surprisingly the use of four equivalents of triphenylphosphine requires a longer reaction time (compare entries I and 3 in Table 1). Kinetic and spectroscopic studies are in progress.
32. 10.1002/macp.1990.02191090210.1002/macp.1990.021910902 ↗
33. The nonlinear optical properties of various polymers functionalized with 2 will be published elsewhere.