Nickel(II) compounds derived from tripod ligands: Efficient catalysts for the stereoselective heterodimerization of styrene and propene

European Journal of Inorganic Chemistry

Volumn , Issue 12, 2003, Pages 2239-2244

  Faissner, Ralf ^a   Huttner, Gottfried ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Catalysis; Heterodimerization; Nickel; Tripod ligands

Indexed keywords

CATALYSTS; LIGANDS; NICKEL COMPOUNDS; PROPYLENE; STEREOSELECTIVITY; STYRENE;

CO CATALYSTS; DONOR SETS; EFFICIENT CATALYSTS; HETERODIMERIZATION; OLEFINS OLIGOMERIZATION; PHOSPHANES; SQUARE-PLANAR COORDINATION; STEREO-SELECTIVE; TETRAHEDRAL COMPOUNDS; TRIPOD LIGANDS;

CATALYSIS;

ALKENE; COORDINATION COMPOUND; LIGAND; METAL COMPLEX; NICKEL COMPLEX; PROPYLENE; STYRENE;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIMERIZATION; GAS CHROMATOGRAPHY; MASS SPECTROMETRY; OLIGOMERIZATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 0037591354     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejic.200200536     Document Type: Article

References (52)

1. For recent reviews see: [1a] P. W. Jolly, G. Wilke, in: Applied Homogenous Catalysis with Organometallic Compounds (Eds.: B. Cornils, W. A. Herrmann), VCH, New York, 1996, vol. 2, p. 1024.
2. [1b] T. V. RajanBabu, in: Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, New York, 1999, vol. 1, p. 417.
3. G. Wilke, Angew. Chem. 1988, 100, 189; Angew. Chem. Int. Ed. Engl. 1988, 27, 185.
4. G. Wilke, Angew. Chem. 1988, 100, 189; Angew. Chem. Int. Ed. Engl. 1988, 27, 185.
5. T. Alderson, E. L. Jenner, R. V. Lindsey, Jr., J. Am. Chem. Soc. 1965, 87, 5638.
6. For Pd-catalysed reactions see: [4a] E. Drent (Shell Oil Company), US Patent 5227561, 1993 (Chem. Abstr. 1994, 120, 31520).
7. [4b] G. J. P. Britovsek, W. Keim, S. Mecking, D. Sainz, T Wagner, J. Chem. Soc., Chem. Commun. 1993, 1632.
8. [4c] G. J. P. Britovsek, K. J. Cavell, W. Keim, J. Mol. Catal. A 1996, 110, 7.
9. [4d] R. Bayersdörfer, B. Ganter, U. Englert, W. Keim, D. Vogt, J. Organomet. Chem. 1998, 552, 187.
10. [4e] N. J. Hovestad, E. B. Eggeling, H. J. Heidbüchel, J. T. B. H. Jastrzebski, U. Kragl, W. Keim, D. Vogt, G. van Koten, Angew. Chem. 1999, 111, 1763; Angew. Chem. Int. Ed. 1999, 38, 1655.
11. N. J. Hovestad, E. B. Eggeling, H. J. Heidbüchel, J. T. B. H. Jastrzebski, U. Kragl, W. Keim, D. Vogt, G. van Koten, Angew. Chem. 1999, 111, 1763; Angew. Chem. Int. Ed. 1999, 38, 1655.
12. [4f] E. B. Eggeling, N. J. Hovestad, J. T. B. H. Jastrzebski, D. Vogt, G. van Koten, J. Org. Chem. 2000, 65, 8857.
13. For Co-catalysed reactions see: [5a] S. M. Pillai, G. L. Tembe, M. Ravindranathan, J. Mol. Catal. 1993, 84, 77. For Ru-catalysed reactions see: [5b] H. Umezaki, Y. Fujiwara, K. Sawara, S. Teranishi, Bull. Chem. Soc. Jpn. 1973, 46, 2230. [5c] C. S. Yi, Z. He, D. W. Lee, Organometallics 2001, 20, 802.
14. For Co-catalysed reactions see: [5a] S. M. Pillai, G. L. Tembe, M. Ravindranathan, J. Mol. Catal. 1993, 84, 77. For Ru-catalysed reactions see: [5b] H. Umezaki, Y. Fujiwara, K. Sawara, S. Teranishi, Bull. Chem. Soc. Jpn. 1973, 46, 2230. [5c] C. S. Yi, Z. He, D. W. Lee, Organometallics 2001, 20, 802.
15. For Co-catalysed reactions see: [5a] S. M. Pillai, G. L. Tembe, M. Ravindranathan, J. Mol. Catal. 1993, 84, 77. For Ru-catalysed reactions see: [5b] H. Umezaki, Y. Fujiwara, K. Sawara, S. Teranishi, Bull. Chem. Soc. Jpn. 1973, 46, 2230. [5c] C. S. Yi, Z. He, D. W. Lee, Organometallics 2001, 20, 802.
16. [6a] N. Kawata, K. Maruya, T. Mizoroki, A. Ozaki, Bull. Chem. Soc Jpn. 1974, 47, 413.
17. [6b] B. Bogdanović, Adv. Organomet. Chem. 1979, 17, 105.
18. [6c] R. Ceder, G. Muller, J. I. Ordinas, J. Mol. Catal. 1994, 92, 127.
19. [6d] A. L. Monteiro, M. Seferin, J. Dupont, R. F. de Souza, Tetrahedron Lett. 1996, 37, 1157.
20. [6e] G. Muller, J. I. Ordinas, J. Mol. Catal. A 1997, 125, 97.
21. [6f] V. Fassina, C. Ramminger, M. Seferin, A. L. Monteiro, Tetrahedron 2000, 56, 7403.
22. [7a] K. Angermund, A. Eckerle, F. Lutz, Z. Naturforsch., Teil B 1995, 50, 488.
23. [7b] N. Nomura, J. Jin, H. Park, T. V. RajanBabu, J. Am. Chem. Soc. 1998, 120, 459.
24. [7c] M. Nandi, J. Jin, T. V. RajanBabu, J. Am. Chem. Soc. 1999, 121, 9899.
25. [7d] T. V. Rajan-Babu, N. Nomura, J. Jin, B. Radetich, H. Park, M. Nandi, Chem. Eur J. 1999, 5, 1963.
26. [7e] J. Jin, T. V. RajanBabu, Tetrahedron 2000, 56, 2145.
27. [7f] A. Bösmann, G. Franciò, E. Janssen, M. Solinas, W. Leitner, P. Wasserscheid, Angew. Chem. 2001, 113, 2769; Angew. Chem. Int. Ed. 2001, 40, 2697.
28. [7f] A. Bösmann, G. Franciò, E. Janssen, M. Solinas, W. Leitner, P. Wasserscheid, Angew. Chem. 2001, 113, 2769; Angew. Chem. Int. Ed. 2001, 40, 2697.
29. [7g] G. Franciò, F. Faraone, W. Leitner, J. Am. Chem. Soc. 2002, 124, 736.
30. [7h] H. Park, T. V. RajanBabu, J. Am. Chem. Soc. 2002, 124, 734.
31. [8a] T. Ito, K. Takahashi, Y. Takami, Nippon Kagaku Kaishi 1974, 1097 (Chem. Abstr 1974, 81, 77567).
32. [8a] T. Ito, K. Takahashi, Y. Takami, Nippon Kagaku Kaishi 1974, 1097 (Chem. Abstr 1974, 81, 77567).
33. [8b] K. Kawakami, N. Kawata, K. Maruya, T. Mizoroki, A. Ozaki, J. Catal. 1975, 39, 134.
34. [8c] A. G. Azizov, K. Z. Mamedov, S. M. Aliev, Sb. Tr. Akad. Nauk Az. SSR, Inst. Neftekhim. Protsessov im. Akad. Yu. G. Mamedalieva 1986, 15, 58 (Chem. Abstr 1988, 108, 131117).
35. [8c] A. G. Azizov, K. Z. Mamedov, S. M. Aliev, Sb. Tr. Akad. Nauk Az. SSR, Inst. Neftekhim. Protsessov im. Akad. Yu. G. Mamedalieva 1986, 15, 58 (Chem. Abstr 1988, 108, 131117).
36. [9a] C. Jeffrey, T. B. Rauchfuss, Inorg. Chem. 1979, 18, 2658.
37. [9b] A. Bader, E. Lindner, Coord. Chem. Rev. 1991, 108, 27.
38. [9c] C. S. Slone, D. A. Weinberger, C. A. Mirkin, Prog. Inorg. Chem. 1999, 48, 233.
39. [10a] R. Faissner, G. Huttner, E. Kaifer, P. Rutsch, Eur. J. Inorg. Chem. 2003, 1681-1693.
40. [10b] R. Faissner, G. Huttner, E. Kaifer, P. Kircher, P. Rutsch, L. Zsolnai, Eur. J. Inorg. Chem. 2003, 2219-2238, preceding paper.
41. [11a] W. Keim, Angew. Chem. 1990, 102, 251; Angew. Chem. Int. Ed. Engl. 1990, 29, 235.
42. [11a] W. Keim, Angew. Chem. 1990, 102, 251; Angew. Chem. Int. Ed. Engl. 1990, 29, 235.
43. [11b] D. Vogt, in: Applied Homogenous Catalysis with Organic Compounds (Eds.: B. Cornils, W. A. Herrmann), VCH, New York, 1996, vol. 1, p. 245.
44. [12a] G. Wilke, B. Bogdanović, P. Hardt, P. Heimbach, W. Keim, M. Kröner, W. Oberkirch, K. Tanaka, E. Steinrücke, D. Walter, H. Zimmermann, Angew. Chem. 1966, 78, 157; Angew. Chem. Int. Ed. Engl. 1966, 5, 151.
45. [12a] G. Wilke, B. Bogdanović, P. Hardt, P. Heimbach, W. Keim, M. Kröner, W. Oberkirch, K. Tanaka, E. Steinrücke, D. Walter, H. Zimmermann, Angew. Chem. 1966, 78, 157; Angew. Chem. Int. Ed. Engl. 1966, 5, 151.
46. [12b] Y. Chauvin, H. Olivier, in: Applied Homogenous Catalysis with Organometallic Compounds (Eds.: B. Cornils, W. A. Herrmann), VCH, New York, 1996, vol. 1, p. 258.
47. [13a] B. Bogdanović, Adv. Organomet. Chem. 1979, 17, 105.
48. [13b] E. Balbolov, M. Mitkova, K. Kurtev, J.-P. Gehrke, R. Taube, J. Organomet. Chem. 1988, 352, 247.
49. [13c] S. A. Svejda, M. Brookhart, Organometallics 1999, 18, 65.
50. H. L. Goering, E. P. Seitz Jr., C. C. Tseng, J. Org. Chem. 1981, 46, 5304.
51. M. F. Lipton, C. M. Sorensen, A. C. Sadler, J. Organomet. Chem. 1980, 186, 155.
52. Orgkanikum, Deutscher Verlag der Wissenschaften, Berlin, 1990.