journal article·1998-05-01

Lewis Acidic Borane Adducts of Pyridines and Stilbazoles for Nonlinear Optics

M. J. Gerald Lesley, Alden Woodward, Nicholas J. Taylor, Todd B. Marder, Iréne Cazenobe, Isabelle Ledoux, Joseph Zyss, Anna Thornton, Duncan W. Bruce, Ashok K. Kakkar

Chemistry of Materials· Volume 10· Issue 5
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Abstract

A series of neutral pyridyl adducts involving the strong Lewis acids BF 3 and B(C 6 F 5 ) 3 has been prepared, and their second-order nonlinear optical coefficients (EFISH method) have been examined. The formation of the pyridyl−boron bond leads to enhancement of the dipole moments and second-order NLO coefficients (β and β(0)). Reactions of DMAP (4-Me 2 N−C 5 H 4 N) with BH 3, BF 3, and B(C 6 F 5 ) 3 give the corresponding neutral pyridine adducts DMAP·BH 3 (orthorhombic, Pbca, a = 9.6914(7) Å; b = 11.7173(9) Å; c = 22.718(2) Å; V = 1622.4(5) Å 3; Z = 8; p = 1.114 g cm - 3 ), DMAP·BF 3 (orthorhombic, Pbca, a = 10.430(3) Å; b = 8.111(2) Å; c = 20.295(7) Å; V = 1717.0(9) Å 3; Z = 8; p = 1.470 g cm - 3 ), and DMAP·B(C 6 F 5 ) 3 (orthorhombic, Pbca, a = 12.322(1) Å; b = 20.556(2) Å; c = 28.455(3) Å; V = 7207.4(14) Å 3; Z = 8; p = 1.508 g cm - 3 ). Reactions of Me 2 N−4-C 6 H 4 −CH CH−C 5 H 4 N, MeO−4-C 6 H 4 −CH CH−C 5 H 4 N, and Me 2 N−4-C 6 H 4 −C⋮C−C 5 H 4 N with BF 3 and B(C 6 F 5 ) 3 result in materials that are highly luminescent and incorporate structural features that are known to give rise to large second-order NLO effects. X-ray diffraction analysis for the compound Me 2 N−4-C 6 H 4 −C⋮C−C 5 H 4 N·B(C 6 F 5 ) 3 (monclinic, P 2 1 / c, a = 9.883(2) Å; b = 10.717(1) Å; c = 28.421(4) Å; β = 91.96(1)°; V = 2993.4(8) Å 3; Z = 4; p = 1.629 g cm - 3 ) is also described.
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Research context

OpenAlex topics: Nonlinear Optical Materials Research · Crystal Structures and Properties · Solid-state spectroscopy and crystallography

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Affiliations

Department of Chemistry, McGill University, Montreal, Quebec, Canada, H3A 2K6

References (53)

Show source-provided references
1. 1987 · 1
2. For reviews involving applications of NLO materials see: (a)Conjugated Polymeric Materials: Opportunities in Electronics,Optoelectronics, and Molecular Electronics; Bredas, J. L., Chance, R. R., Eds.; NATO ARW Series E182; Kluwer Academic Publishers: Dordrecht, 1990. (b)Materials for Nonlinear Optics: Chemical Perspectives; Marder, S. R., Sohn, J. E., Stucky, G. D., Eds.; ACS Symp. Ser. 455; American Chemical Society: Washington, DC, 1991. (c)Molecular Nonlinear Optics: Materials, Physics, and Devices; Zyss, J., Ed.; Academic Press: New York, 1994. (d)Nonlinear Optical Properties of Organic Materials VII; Mohlmann, G. R., Ed.; Proc. SPIE, Vol. 2285; The International Society for Optical Engineering: Washington, DC, 1994. (e)Organic, Metallo-Organic,and Polymeric Materials for Nonlinear Optical Applications; Marder, S. R., Perry, J. W., Eds.; Proc. SPIE, Vol. 2143; The International Society for Optical Engineering: Washington, DC, 1994.
3. Marder S. R. · Chem. Mater. · 1994 · 6 · 113710.1021/cm00044a012 ↗
4. Hubbard M. A. · Chem. Mater. · 1989 · 1 · 16710.1021/cm00002a001 ↗
5. Nguyen P. · Inorg. Chim. Acta · 1994 · 220 · 28910.1016/0020-1693(94)03881-3 ↗
6. (b) Marder, T. B.; Lesley, G.; Yuan, Z.; Fyfe, H. B.; Chow, P.; Stringer, G.; Jobe, I. R.; Taylor, N. J.; Williams, I. D.; Kurtz, S. K. In ref 2b, p 605.
7. (c) Nguyen, P.; Lesley, G.; Dai, C.; Taylor, N. J.; Marder, T. B.; Chu, V.; Viney, C.; Ledoux, I.; Zyss, J. InApplications ofOrganometallic Chemistry in the Preparation and Processing of AdvancedMaterials; Harrod, J. F., Laine, R. M., Eds.; NATO ASI Series E; Kluwer Academic Publishers: Dordrecht, 1995; Vol. 297, p 333.10.1007/978-94-011-0337-4_19 ↗
8. Nguyen P. · Chem. Mater. · 1997 · 9 · 40610.1021/cm960449k ↗
9. Cheng L.-T. · J. Phys. Chem. · 1991 · 95 · 1063110.1021/j100179a026 ↗
10. J. Phys. Chem. · 1991 · 95 · 10634
11. Dirk C. W. · Chem. Mater. · 1990 · 2 · 70010.1021/cm00012a020 ↗
12. Jen A. K.-Y. · J. Chem. Soc., Chem. Commun. · 1993 · 9010.1039/c39930000090 ↗
13. Rao V. P. · J. Ibid. · 1993 · 1118
14. Rao V. P. · J. Ibid. · 1994 · 1689
15. Jen A. K.-Y. · J. Ibid. · 1994 · 2057
16. Kurihara T. · J. Chem. Soc., Chem. Commun. · 1987 · 95910.1039/C39870000959 ↗
17. Tabei H. · Appl. Phys. Lett. · 1987 · 50 · 18510.1063/1.97716 ↗
18. Steigman A. E. · J. Am. Chem. Soc. · 1987 · 109 · 588410.1021/ja00253a070 ↗
19. Steigman A. E. · J. Am. Chem. Soc. · 1991 · 113 · 765810.1021/ja00020a030 ↗
20. Perry J. W. · 17
21. (f) Steigman, A. E.; Perry, J. W.; Cheng, L.T. In ref 1d, p 149.
22. Dehu C. · J. Am. Chem. Soc. · 1993 · 115 · 619810.1021/ja00067a039 ↗
23. Etter M. C. · Chem. Mater. · 1989 · 1 · 1010.1021/cm00001a005 ↗
24. (b) Etter, M. C.; Huang, K. S.; Frankenbach, G. M.; Adsmond, D. A. In ref 2b, p 457.
25. Etter M. C. · J. Phys. Chem. · 1991 · 95 · 460110.1021/j100165a007 ↗
26. Blanchard-Desce M. · J. Chem. Soc., Chem. Commun. · 1988 · 73710.1039/C39880000737 ↗
27. (b) Blanchard-Desce, M.; Lehn, J.M.; Ledoux, I.; Zyss, J. In ref 1c, p 170.
28. (c) Zyss, J.; Ledoux, I.; Nicoud, J.F. In ref 2c, p 129.
29. Marder S. R. · Science · 1994 · 263 · 51110.1126/science.263.5146.511 ↗
30. Meredith, G. R. In ref 1a, p 27.
31. Bruce D. W. · Adv. Mater. Opt. Electron. · 1994 · 4 · 29310.1002/amo.860040409 ↗
32. Cheng L.-T. · Organometallics · 1990 · 9 · 285610.1021/om00161a003 ↗
33. Cheng L.-T. · Mol. Cryst. Liq. Cryst. · 1990 · 189 · 137
34. Kanis D. R. · J. Am. Chem. Soc. · 1994 · 116 · 1008910.1021/ja00101a030 ↗
35. Bruce D. W. · Mol. Cryst. Liq. Cryst. · 1993 · 231 · 25310.1080/10587259308032510 ↗
36. Bruce D. W. · Liq. Cryst. · 1988 · 3 · 38510.1080/02678298808086385 ↗
37. 1996
38. Bourgault M. · J. Chem. Soc., Chem. Commun. · 1993 · 162310.1039/c39930001623 ↗
39. Peng Z. · J. Am. Chem. Soc. · 1996 · 118 · 377710.1021/ja953231s ↗
40. Yuan Z. · J. Chem. Soc., Chem. Commun. · 1990 · 148910.1039/C39900001489 ↗
41. (b) Yuan, Z.; Taylor, N. J.; Marder, T. B.; Williams, I. D.; Kurtz, S. K.; Cheng, L.T. In ref 1d, p 190.
42. Yuan Z. · J. Organomet. Chem. · 1993 · 449 · 2710.1016/0022-328X(93)80103-I ↗
43. Yuan Z. · Appl. Organomet. Chem. · 1996 · 10 · 30510.1002/(SICI)1099-0739(199604)10:3/4<305::AID-AOC463>3.0.CO;2-G ↗
44. Lequan M. · J. Mater. Chem. · 1991 · 1 · 99710.1039/JM9910100997 ↗
45. Lequan M. · J. Mater. Chem. · 1992 · 2 · 71910.1039/jm9920200719 ↗
46. For · J. Organomet. Chem. · 1964 · 2 · 24510.1016/S0022-328X(00)80518-5 ↗
47. Guggenheim E. A. · Trans. Faraday Soc. · 1949 · 45 · 20310.1039/tf9494500714 ↗
48. Chem Window 0. · 1990
49. Recently · Angew. Chem., Int. Ed. Engl. · 1996 · 35 · 64410.1002/anie.199606441 ↗
50. Kurtz S. K. · J. Appl. Phys. · 1968 · 39 · 379810.1063/1.1656857 ↗
51. Zyss J. · J. Chem. Phys. · 1981 · 74 · 480010.1063/1.441759 ↗
52. Ohms U. · Z. Kristallogr. · 1983 · 162 · 17410.1524/zkri.1983.162.1-4.299 ↗
53. Ohms U. · Z. Kristallogr. · 1984 · 166 · 21310.1524/zkri.1984.166.3-4.213 ↗