Diphosphines with expandable bite angles: Highly active ethylene dimerisation catalysts based on upper rim, distally diphosphinated calix[4]arenes

Chemistry - A European Journal

Volumn 10, Issue 21, 2004, Pages 5354-5360

  Lejeune, Manuel ^a   Sémeril, David ^a   Jeunesse, Catherine ^a   Matt, Dominique ^a   Peruch, Frédéric ^b   Lutz, Pierre J ^b   Ricard, Louis ^c  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b INSTITUT CHARLES SADRON   (France)

^c ECOLE POLYTECHNIQUE   (France)

Author keywords

Calixarenes; Ethylene dimerisation; Molecular dynamics; Nickel; P ligands

Indexed keywords

CATALYSTS; CHELATION; CHEMICAL ACTIVATION; CONCENTRATION (PROCESS); DIMERS; LOW TEMPERATURE EFFECTS; NICKEL; NUCLEAR MAGNETIC RESONANCE; OLIGOMERS; THERMAL EFFECTS; X RAY ANALYSIS;

CATALYST CONCENTRATION; LIGANDS; OLIGOMERIZATION;

ETHYLENE;

1 BUTENE; 5,17 BIS(DIPHENYLPHOSPHINO) 25,26,27,28 TETRAPROPOXYCALIX[4]ARENE; 5,17 DIBROMO 11,23 BIS(DIPHENYLPHOSPHINO) 25,26,27,28 TETRAPROPOXYCALIX[4]ARENE; ALKENE; BORON DERIVATIVE; CALIX[4]ARENE DERIVATIVE; CALIXARENE; CHELATE; COORDINATION COMPOUND; DIPHOSPHINE DERIVATIVE; ETHYLENE; LIGAND; METAL; NICKEL; PHOSPHINE DERIVATIVE; PHOSPHORUS DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL BINDING; CHEMICAL BOND; COMPLEX FORMATION; CONCENTRATION (PARAMETERS); CRYSTAL STRUCTURE; DIMERIZATION; LOW TEMPERATURE; MOLECULAR DYNAMICS; OLIGOMERIZATION; OSCILLATION; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PROTON NUCLEAR MAGNETIC RESONANCE; SOLID STATE; X RAY ANALYSIS;

EID: 8344249411     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200400492     Document Type: Article

References (53)

1. V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745.
2. V. Böhmer, Angew. Chem. 1995, 107, 785-818; Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745.
3. C. Wieser, C. B. Dieleman, D. Matt, Coord. Chem. Rev. 1997, 165, 93-161.
4. C. D. Gutsche, Calixarenes Revisited, Monographs in Supramolecular Chemistry (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1998.
5. C. Dieleman, C. Marsol, D. Matt, N. Kyritsakas, A. Harriman, J.-P. Kintzinger, J. Chem. Soc. Dalton Trans. 1999, 4139-4148.
6. Calixarenes in Action, (Eds.: L. Mandolini, R. Ungaro), Imperial College Press, London, 2000.
7. Calixarenes 2001 (Eds.: Z. Asfari, V. Böhmer, J. Harrowfield, J. Vicens), Kluwer, Dordrecht, 2001.
8. A. Arduini, A. Casnati, L. Dodi, A. Pochini, R. Ungaro, J. Chem. Soc., Chem. Commun. 1990, 1597-1598.
9. E. van Dienst, W. I. I. Bakker, J. F. J. Engbersen, W. Verboom, D. N. Reinhoudt, Pure Appl. Chem. 1993, 65, 387-392.
10. A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734.
11. P. Schmitt P. D. Beer, M. G. B. Drew, P. D. Sheen, Angew. Chem. 1997, 109, 1926-1928; Angew. Chem. Int. Ed. Engl. 1997, 36, 1840-1842.
12. P. Schmitt P. D. Beer, M. G. B. Drew, P. D. Sheen, Angew. Chem. 1997, 109, 1926-1928; Angew. Chem. Int. Ed. Engl. 1997, 36, 1840-1842.
13. C. Wieser, D. Matt, J. Fischer, A. Harriman, J. Chem. Soc. Dalton Trans. 1997, 2391-2402.
14. R. Paciello, L. Siggel, M. Röper, Angew. Chem. 1999, 111, 2045-2048; Angew. Chem. Int. Ed. 1999, 38, 1920-1923.
15. R. Paciello, L. Siggel, M. Röper, Angew. Chem. 1999, 111, 2045-2048; Angew. Chem. Int. Ed. 1999, 38, 1920-1923.
16. R. A. Kemp, D. S. Brown, M. Lattman, J. Li, J. Mol. Catal. A: Chem. 1999, 149, 125-133.
17. C. J. Cobley, D. D. Ellis, A. G. Orpen, P. G. Pringle, J. Chem. Soc. Dalton Trans. 2000, 1109-1112.
18. F. J. Parlevliet, C. Kiener, J. Fraanje, K. Goubitz, M. Lutz, A. L. Spek, P. C. J. Kamer, P. W. N. M. van Leeuwen, J. Chem. Soc. Dalton Trans. 2000, 1113-1122.
19. C. Dieleman, S. Steyer, C. Jeunesse, D. Matt, J. Chem. Soc. Dalton Trans. 2001, 2508-2517.
20. V. C. Gibson, C. Redshaw, M. R. J. Elsegood, J. Chem. Soc. Dalton Trans. 2001, 767-769.
21. X. Fang, B. L. Scott, J. G. Watkin, C. A. G. Carter, G. J. Kubas, Inorg. Chim. Acta 2001, 317, 276-281.
22. Y. Chen, Y. Zhang, Z. Shen, R. Kou, L. Chen, Eur. Polym. J. 2001, 37, 1181-1184.
23. S. Steyer, C. Jeunesse, D. Matt, R. Welter, M. Wesolek, J. Chem. Soc. Dalton Trans. 2002, 4264-4274.
24. C. Kunze, D. Selent, I. Neda, M. Freytag, P. G. Jones, R. Schmutzler, W. Baumann, A. Börner, Z. Anorg. Allg. Chem. 2002, 628, 779-787.
25. F. Plourde, K. Gilbert, J. Gagnon, P. D. Harvey, Organometallics 2003, 22, 2862-2875.
26. C. Capacchione, P. Neri, A. Proto, Inorg. Chem. Commun. 2003, 6, 339-342.
27. M. Frank, G. Maas, J. Schatz, Eur. J. Org. Chem. 2004, 607-613.
28. C. Wieser-Jeunesse, D. Matt, A. De Cian, Angew. Chem. 1998, 110, 3027-3030; Angew. Chem. Int. Ed. Engl. 1998, 37, 2861-2864.
29. C. Wieser-Jeunesse, D. Matt, A. De Cian, Angew. Chem. 1998, 110, 3027-3030; Angew. Chem. Int. Ed. Engl. 1998, 37, 2861-2864.
30. M. Lejeune, C. Jeunesse, D. Matt, N. Kyritsakas, R. Welter, J.-P. Kintzinger, J. Chem. Soc., Dalton Trans. 2002, 1642-1650.
31. J. Gagnon, M. Vézina, M. Drouin, P. D. Harvey, Can. J. Chem. 2001, 79, 1439-1446.
32. P. D. Harvey, Coord. Chem. Rev. 2002, 233-234, 289-309.
33. A. J. Evans, S. E. Matthews, A. R. Cowley, P. D. Beer, Dalton Trans. 2003, 4644-4650.
34. J. R. Ascenso, A. R. Dias, M. T. Duarte, P. T. Gomes, J. N. Marote, A. F. G. Ribeiro, J. Organomet. Chem. 2001, 632, 164-174.
35. -1]; see H. Günther, NMR-Spektroskopie, 3rd ed., Thieme, Stuttgart, 1992, pp. 309-310.
36. SPARTAN, Version 1.1.8, Wawefunction, Inc., Irvine (USA), 1997.
37. K. Takenaka, Y. Obora, L. H. Jiang, Y. Tsuji, Organometallics 2002, 21, 1158-1166.
38. D. Commereuc, Y. Chauvin, G. Léger, J. Gaillard, Rev. Inst. Fr. Pet. 1982, 37, 639-649.
39. S. Muthukumaru Pillai, M. Ravindranathan, S. Sivaram, Chem. Rev. 1986, 86, 353-399.
40. A. Carter, N. A. Cooley, P. G. Pringle, J. Scutt, D. F. Wass, Polym. Mater. Sci. Eng. 2002, 86, 314-315.
41. V. C. Gibson, S. K. Spitzmesser, Chem. Rev. 2003, 103, 283-315.
42. N. A. Cooley, S. M. Green, D. F. Wass, K. Heslop, A. G. Orpen, P. G. Pringle, Organometallics 2001, 20, 4769-4771.
43. S. J. Brown, A. F. Masters, J. Organomet. Chem. 1989, 367, 371-374.
44. J. M. Malinoski, M. Brookhart, Organometallics 2003, 22, 5324-5335.
45. F. Speiser, P. Braunstein, L. Saussine, R. Welter, Inorg. Chem. 2004, 43, 1649-1658.
46. H. D. Mui, M. E. Riehl, S. R. Wilson, G. S. Girolami, ACS Abstracts, Vol. 208 (part 1) 1994, 530-INOR.
47. H. Makio, N. Kashiwa, T. Fujita, Adv. Synth. Catal. 2002, 344, 477-493.
48. M. Mitani, T. Fujita, ACS Symp. Ser. 2003, 857, 26-45.
49. A. Salzer, T. L. Court, H. Werner, J. Organomet. Chem. 1973, 54, 325-330.
50. P.-G. Lassahn, V. Lozan, B. Wu, A. S. Weller, C. Janiak, Dalton Trans. 2003, 4437-4450.
51. A. Altomare, M. C. Burla, M. Camalli, G. Cascarano, C. Giacovazzo, A. Guagliardi, A. G. G. Moliterni, G. Polidori, R. Spagna, SIR97, an integrated package of computer programs for the solution and refinement of crystal structures using single-crystal data.
52. G. M. Sheldrick, SHELXL-97, Program for Crystal Structure Refinement, University of Göttingen, Göttingen, Germany, 1997.
53. PLATON, A multipurpose Crystallographic Tool, version 1999, Utrecht University, Utrecht, The Netherlands, 1999.