Two 1D [CuxIx]-based coordination polymers of tetraphosphine ligands

Inorganic Chemistry Communications

Volumn 12, Issue 10, 2009, Pages 1031-1034

  Li, Ni Ya ^a   Ren, Zhi Gang ^a   Liu, Dong ^a   Wang, Jing ^a   Dai, Ming ^a   Li, Hong Xi ^a   Lang, Jian Ping ^a,b  

^a SOOCHOW UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Coordination polymer; Copper(I); Crystal structure; Tetraphosphine

Indexed keywords

EID: 70349411504     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2009.08.014     Document Type: Article

References (31)

1. Hierso J.C., Amardeil R., Bentabet E., Broussier R., Gautheron B., Meunier P., and Kalck P. Coord. Chem. Rev. 236 (2003) 143
2. Hierso J.C., Fihri A., Ivanov V.V., Hanquet B., Pirio N., Donnadieu B., Rebiere B., Amardeil R., and Meunier P. J. Am. Chem. Soc. 126 (2004) 11077
3. Effendy, Nicola C.D., Fianchini M., Pettinari C., Skelton B.W., Somers N., and White A.H. Inorg. Chim. Acta 358 (2005) 763
4. Zhang J.F., Yu M.M., Zhao X.J., Qu X.M., and Fu W.F. Acta Cryst. E62 (2006) m3498
5. Neo S.P., Zhou Z.Y., Mark T.C.W., and Hor T.S.A. Dalton Trans. (1994) 3451
6. Kohl S.W., Heinemann F.W., Hummert M., Bauer W., and Grohmann A. Dalton Trans. (2006) 5583
7. Saravanabharathi D., Monika, Venugopalan P., and Samuelson A.G. Polyhedron 21 (2002) 2433
8. Rodriguez-Zubiri M., Gallo V., Rose J., Welter R., and Braunstein P. Chem. Commun. (2008) 64
9. Xu X.L., Nieuwenhuyzen M., and James S.L. Angew. Chem., Int. Ed. 41 (2002) 764
10. Zhang J., Miller P.W., Nieuwenhuyzen M., and James S.L. Chem. Eur. J. 12 (2006) 2448
11. Zhang J., Nieuwenhuyzen M., Charmant J.P.H., and James S.L. Chem. Commun. (2004) 2808
12. Zhang J., Xu X.L., and James S.L. Chem. Commun. (2006) 4218
13. James S.L., Mingos D.M.P., White A.J.P., and Williams D.J. Chem. Commun. (1998) 2323
14. Miller P.W., Nieuwenhuyzen M., Charmant J.P.H., and James S.L. Inorg. Chem. 47 (2008) 8367
15. Ganesamoorthy C., Balakrishna M.S., Mague J.T., and Tuononen H.M. Inorg. Chem. 47 (2008) 7035
16. Bianchini C., Meli A., Peruzzini M., Vizza F., Moneti S., Herrera V., and Sanchez-Delgado R.A. J. Am. Chem. Soc. 116 (1994) 4370
17. Balch A.L., Olmstead M.M., and Rowley S.P. Inorg. Chim. Acta 168 (1990) 255
18. Zhang J.Y., Vittal J.J., Henderson W., Wheaton J.R., Hall I.H., Hor T.S.A., and Yan Y.K. J. Organomet. Chem. 650 (2002) 123
19. Song L.C., Su F.H., Hu Q.M., Grigiotti E., and Zanello P. Eur. J. Inorg. Chem. (2006) 422
20. Fernández E.J., Laguna A., López-de-Luzuriaga J.M., Monge M., Montiel M., Olmos M.E., Puelles R.C., and Sánchez-Forcada E. Eur. J. Inorg. Chem. (2007) 4001
21. Li L., Ren Z.G., Li N.Y., Zhang Y., and Lang J.P. Inorg. Chim. Acta 362 (2009) 3910
22. Chen J.X., Tang X.Y., Chen Y., Zhang W.H., Li L.L., Yuan R.X., Zhang Y., and Lang J.P. Cryst. Growth Des. 9 (2009) 1461
23. 2).
24. 2 = 0.1311 and S = 1.107 based on 4234 observed reflections with I > 2.00σ(I). Data collections were performed on a Rigaku Mercury CCD diffractomer with graphite-monochromated Mo Kα radiation (λ = 0.71073 Å). The crystal structures were solved by direct methods and refined with full-matrix least-squares technique using SHELXL-97 program [25]. All non-hydrogen atoms were refined anisotropically. Hydrogen atoms were placed in geometrically idealized positions and constrained to ride on their parent atoms.
25. Sheldrick G.M. Acta Cryst. A 64 (2008) 112
26. Tsuboyama A., Kuge K., Furugori M., Okada S., Hoshino M., and Ueno K. Inorg. Chem. 46 (2007) 1992
27. Cariati E., Roberto D., Ugo R., Ford P.C., Galli S., and Sironi A. Inorg. Chem. 44 (2005) 4077
28. Wu T., Li M., Li D., and Huang X.C. Cryst. Growth Des. 44 (2007) 4077
29. Churchill M.R., DeBoer B.G., and Donovan D.J. Inorg. Chem. 14 (1975) 617
30. Mason M.R., Duff C.M., Miller L.L., Jacobson R.A., and Verkade J.G. Inorg. Chem. 31 (1992) 2746
31. Feeder N., Geng J.F., Goh P.G., Johnson B.F.G., Martin C.M., Shephard D.S., and Zhou W.Z. Angew. Chem., Int. Ed. 39 (2000) 1661