Trimer Porphyrin Star

Yulia P. Yaschuk, Vladimir S. Tyurin and Irina P. Beletskaya^@

A.N. Frumkin Institute of Physical Chemistry and Electrochemistry of Russian Academy of Sciences, 119071 Moscow,
Russian Federation

^@E-mail: beletska@org.chem.msu.ru

Macroheterocycles 2012 5(4-5) 302-307

DOI: 10.6060/mhc2012.121199b

A novel tripod star-shaped porphyrin trimer has been synthesized using “click” methodology. It was shown that it can coordinate DABCO and Bipy forming cofacial dimer aggregates.

References

Click here to expand or collapse this section

1. The Porphyrin Handbook, Vol. 6 Applications: Past, Present and Future (Kadish K. M., Smith K., Guillard R. Eds.), San Diego: Academic, 2000.

2. Takai A., Chkounda M.; Eggenspiller A., Gros C. P.; Lachkar M., Barbe J.-M., Fukuzumi S. J. Am. Chem. Soc., 2010, 132 (12), 4477-4489.
http://dx.doi.org/10.1021/ja100192x

3. Takai A., Gros C. P., Barbe J.-M., Fukuzumi S. Chemistry - A European Journal, 2011, 17 (12), 3420-3428.
http://dx.doi.org/10.1002/chem.201002822

4. Takase M., Yoshida N., Nishinaga T., Iyoda M. Organic Letters 2011, 13 (15), 3896-3899.
http://dx.doi.org/10.1021/ol2014279

5. Tong L. H., Pascu S. I., Jarrosson T., Sanders J. K. M. Chem. Commun., 2006, (10), 1085-1087.
http://dx.doi.org/10.1039/b515902d

6. Xie Y., Akada M., Hill J. P., Ji Q., Charvet R., Ariga K. Chem. Commun., 2011, 47 (8), 2285-2287.
http://dx.doi.org/10.1039/c0cc04855k

7. Campbell W. M., Burrell A. K., Officer D. L., Jolley K. W. Coordination Chemistry Reviews, 2004, 248, 1363–1379.
http://dx.doi.org/10.1016/j.ccr.2004.01.007

8. Shinmori H., Kajiwara T., Osuka A. Tetrahedron Letters, 2001, 42, 3617–3620.
http://dx.doi.org/10.1016/S0040-4039(01)00520-2

9. Beletskaya I., Tyurin V. S., Tsivadze A. Y., Guilard R., Stern C. Chemical Reviews, 2009, 109 (5), 1659-1713.
http://dx.doi.org/10.1021/cr800247a

10. Drain C. M., Varotto A., Radivojevic I. Chemical Reviews, 2009, 109 (5), 1630-1658.
http://dx.doi.org/10.1021/cr8002483

11. Chow H.-F., Lau K.-N., Ke Z., Liang Y., Lo C.-M. Chem. Commun., 2010, 46, 3437.
http://dx.doi.org/10.1039/c0cc00083c

12. Li Y., Flood A. H. Angew. Chem. Int. Ed., 2008, 47, 2649
http://dx.doi.org/10.1002/anie.200704717

13. Juwarker H., Lenhardt J. M., Pham D. M., Craig S. L. Angew. Chem. Int. Ed., 2008, 47, 3740.
http://dx.doi.org/10.1002/anie.200800548

14. Séverac M., Le Pleux L., Scarpaci A., Blart E., Odobel F. Tett. Lett., 2007, 6518-6522.
http://dx.doi.org/10.1016/j.tetlet.2007.07.049

15. Shen D.-M., Liu C., Chen Q.-Y. Eur. J. Org. Chem., 2007, 1419-1422.
http://dx.doi.org/10.1002/ejoc.200601046

16. Shetti V. S., Ravikanth M. Eur. J. Org. Chem., 2010, 494–508.
http://dx.doi.org/10.1002/ejoc.200901070

17. HyperChem Release 8.0.9 for Windows, Hypercube, Inc., USA, (http://www.hyper.com), 2011.

18. Dilek D. K., Huma Z. S., Lindsey J. S. J. Org. Chem., 2007, 72, 7701-7714.
http://dx.doi.org/10.1021/jo701294d

19. Benjamin L., Miller M. A., Lindsey J. S. J. Org. Chem., 1999, 64, 1391-1396.
http://dx.doi.org/10.1021/jo982015+

20. Joydev L. K., Savithri D., Lindsey J. S. Org. Process Res. Dev., 2003, 7, 799-812.
http://dx.doi.org/10.1021/op034083q

21. Uhl W., Bock H. R., Breher F., Claesener M., Haddadpour S., Jasper B., Hepp A. Organometallics, 2007, 26 (9), 2363–2369.
http://dx.doi.org/10.1021/om061118c

22. Benjamin L., Yangzhen C., Lindsey J. S. J. Org. Chem., 1999, 64, 2864.
http://dx.doi.org/10.1021/jo982452o

23. Michael F. A., Lee O. P., Schuster D. I. Org. Lett., 2008, 10, 4979-4982.
http://dx.doi.org/10.1021/ol702922c

24. Cecioni S., Sophie F., Vidal S., Chem. Eur. J., 2011, 17, 2146-2159;
http://dx.doi.org/10.1002/chem.201002635

25. L. Xien, L. Jianhui, S. Licheng, Tetrahedron, 2005, 61, 5655-5662.
http://dx.doi.org/10.1016/j.tet.2005.03.060

26. Lindsey J. S., Brown P. A., Siesel D. A. Tetrahedron, 1989, 45, 4845-4866.
http://dx.doi.org/10.1016/S0040-4020(01)85156-5

27. Bock V. D., Hiemstra H., van Maarseveen J. H. Eur. J. Org. Chem., 2006, 51-68.
http://dx.doi.org/10.1002/ejoc.200500483

28. Kim Y. H., Jeong D. H., Osuka A. J. Am. Chem. Soc., 2001, 123, 76-86.
http://dx.doi.org/10.1021/ja0009976

29. Cho H. S., Song N. W., Osuka A. J. Phys. Chem. A, 2000, 104, 3287-3298.
http://dx.doi.org/10.1021/jp9942623

30. Wook H., Atsuhiro O., Dongho K. J. Am. Chem. Soc., 2004, 126, 16187-16198.
http://dx.doi.org/10.1021/ja046241e

31. Ballester P., Oliva A. I., Costa A., Deya P. M., Frontera A., Gomila R. M., Hunter C. A. J. Am. Chem. Soc., 2006, 128, 5560–5569.
http://dx.doi.org/10.1021/ja060608t

Attachment	Size
mhc2012_t05n4-5_302-307.pdf	839.97 KB

Журнал "Макрогетероциклы"

Navigation

Languages

News

Search