Synthesis of a diimidazolylporphyrin pincer palladium complex

Journal of Porphyrins and Phthalocyanines

Volumn 15, Issue 7-8, 2011, Pages 534-538

  Yamamoto, Jun ^a   Shimizu, Tomohiro ^a   Yamaguchi, Shigeru ^a   Aratani, Naoki ^a   Shinokubo, Hiroshi ^b   Osuka, Atsuhiro ^a  

^a KYOTO UNIVERSITY   (Japan)

^b NAGOYA UNIVERSITY   (Japan)

Author keywords

complexes; cross coupling; Heck reaction; palladacycles

Indexed keywords

EID: 80053101913     PISSN: 10884246     EISSN: None     Source Type: Journal    
DOI: 10.1142/S1088424611002908     Document Type: Article

References (24)

1. Albrecht M and van Koten G. Angew. Chem. Int. Ed. 2001 40 3750-3781.
2. Dupont J, Consorti CS and Spencer J. Chem. Rev. 2005; 105: 2527-2571.
3. van der Boom ME and Milstein D. Chem. Rev. 2003 103 1759-1792.
4. Singleton JT. Tetrahedron 2003; 59: 1837-1857.
5. Yamaguchi S, Katoh T, Shinokubo H and Osuka A. J. Am. Chem. Soc. 2007; 129: 6392-6393.
6. For porphyrin pincer complexes without a direct carbon-metal bond to the porphyrin core, see: A) Suijkerbuijk BMJM, Herreras Martínez SD, van Koten G and Klein Gebbink RJM Organometallics 2008 27 534-542.
7. Suijkerbuijk BMJM, Lutz M, Spek AL, van Koten G and Klein Gebbink RJM. Org. Lett. 2004; 6: 3023-3026.
8. Suijkerbuijk BMJM, Tooke DM, Lutz M, Spek AL, Jenneskens LW, van Koten G and Klein Gebbink RJM. J. Org. Chem. 2010; 75: 1534-1549.
9. Arnold DP, Sakata Y, Sugiura K and Worthington EI. Chem. Commun. 1998; 2331-2332.
10. Hartnell RD and Arnold DP. Organometallics 2004; 23, 391-399.
11. Hartnell RD and Arnold DP. Eur. J. Inorg. Chem. 2004; 1262-1269.
12. Hodgson MJ, Healy PC, Williams ML and Arnold DP. J. Chem. Soc. Dalton Trans 2002; 4497-4504.
13. Arnold DP, Healy PC, Hodgson MJ and Williams ML. J. Organomet. Chem. 2000; 607: 41-50.
14. Atefi F and Arnold DP. J. Porphyrins Phthalocyanines 2008; 12: 801-831.
15. For reviews on organometallic porphyrins, see: Klein Gebbink RJM and Suijkerbuijk BMJM. Angew. Chem. Int. Ed. 2008 47 7396-7421.
16. For cyclometallated porphyrins, see: A) Yamaguchi S, Katoh T, Shinokubo H and Osuka A. J. Am. Chem. Soc. 2008; 130: 14440-14441.
17. Yamaguchi S, Shinokubo H and Osuka A. Inorg. Chem. 2009; 48: 795-797.
18. Matano Y, Matsumoto K, Nakano Y, Uno H, Sakaki S and Imahori H. J. Am. Chem. Soc. 2008; 130: 4588-4589.
19. a) Hata H, Shinokubo H and Osuka A. J. Am. Chem. Soc. 2005; 127: 8264-8265.
20. Hata H, Yamaguchi S, Mori G, Nakazono S, Katoh T, Takatsu K, Hiroto S, Shinokubo H and Osuka A. Chem. Asian J. 2007; 2: 849-859.
21. For the use of NCN type pincer catalysts for Heck reaction, see: A) Takenaka K, Minakawa M and Uozumi Y. J. Am. Chem. Soc. 2005; 127: 12273-12281.
22. Jung IG, Son SU, Park KH, Chung KC, Lee JW and Chung YK. Organometallics 2003; 22: 4715-4720.
23. Soro B, Stoccoro S, Minghetti G, Zucca A, Cinellu MA, Gladiali S, Manassero M and Sansoni M. Organometallics 2005; 24: 53-61.
24. Dijkstra HP, Slagt MQ, McDonald A, Kruithof CA, Kreiter R, Mills AM, Lutz M, Spek AL, Klopper W, van Klink GPM and van Koten G. Eur. J. Inorg. Chem. 2003; 830-838.