β-Functionalized ethylchalcogenolate complexes of lead(II): Synthesis, structures and their conversion into lead chalcogenide nanoparticles

Polyhedron

Volumn 28, Issue 13, 2009, Pages 2749-2753

  Kedarnath, Gotluru ^a   Kumbhare, Liladhar B ^a   Dey, Sandip ^a   Wadawale, Amey P ^a   Jain, Vimal K ^a   Dey, Goutam K ^a  

^a BHABHA ATOMIC RESEARCH CENTRE   (India)

Author keywords

Crystal structure; Lead selenolate; Nanoparticles; PbSe; TEM

Indexed keywords

IV-VI SEMICONDUCTORS; LEAD COMPOUNDS; NANOPARTICLES; SELENIUM COMPOUNDS; SINGLE CRYSTALS; SYNTHESIS (CHEMICAL); X RAY DIFFRACTION ANALYSIS;

CRYSTALS STRUCTURES; DIFFRACTION ANALYSIS; FUNCTIONALIZED; HOMOLEPTIC; LEAD CHALCOGENIDES; LEAD SELENOLATE; NMR DATA; TEM; TRIGONAL BIPYRAMIDAL; X- RAY DIFFRACTIONS;

CRYSTAL STRUCTURE;

EID: 68349125189     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.poly.2009.05.054     Document Type: Article

References (47)

1. Borgstrom P., Ellis L.M., and Reid E.E. J. Am. Chem. Soc. 51 (1929) 3649
2. Shaw R.A., and Woods H. J. Chem. Soc. A (1971) 1569
3. Dance I.G. Polyhedron 5 (1986) 1037
4. J. Parr, in: G.F.R. Perkin, Comprehensive Coordination Chemistry-II, vol. 3 (J.A. McCleverty, T.J. Meyer (Eds.)), Elesevier Ltd., Oxford, 2004, p. 545 (Chapter 3.7).
5. Tieknik E.R.T., and Haiduc I. Prog. Inorg. Chem. 54 (2005) 127
6. Heard P.J. Prog. Inorg. Chem. 53 (2005) 1
7. Haiduc I., Sowerby D.B., and Lu S.F. Polyhedron 14 (1995) 3389
8. Abel E.W. J. Chem. Soc. (1960) 4406
9. Hoffmann G.G. Z. Naturforsch. Teil B 40 (1985) 335
10. Singhal A., and Jain V.K. J. Organomet. Chem. 494 (1995) 75
11. Acharya S., Gautam U.K., Sasaki T., Bando Y., Golan Y., and Ariga K. J. Am. Chem. Soc. 130 (2008) 4594
12. Fleischer H., and Schollmeyer D. Inorg. Chem. 43 (2004) 5529
13. Fan D., Afzal M., Mallik M.A., Nguyen C.Q., O'Brien P., and Thomas P.J. Coord. Chem. Rev. 251 (2007) 1878
14. Garcia-Montalvo V., Cea-Olivares R., and Espinosa-Perez G. Polyhedron 15 (1996) 829
15. Casas J.S., Casteineiras A., Haiduc I., Sanchez A., Sordo J., and Vazquez-Lopez E.M. Polyhedron 13 (1994) 2873
16. Garcia-Montalvo V., Novosad J., Kilian P., Woollins J.D., Slawin A.M.Z., Garcia P.G., Lopez-Cardoso M., Espinosa-Perez G., and Cea-Olivares R. J. Chem. Soc., Dalton Trans. (1997) 1025
17. Ellinson R., Beard M., Johnson J., Yu P., Micic O., Nozik A., Shabaev A., and Efros A. Nano Lett. 5 (2005) 865
18. McDonald S.A., Konstantatos G., Zhang S., Cyr P.W., Klen E.J.D., Levina L., and Sargent E.H. Nat. Mater. 4 (2005) 138
19. Sargent E.H. Adv. Mater. 17 (2005) 515
20. Harrison M.T., Kershaw S.V., Burt M.G., Rogach A.L., Komowski A., Eychmüller A., and Weller H. Pure Appl. Chem. 73 (2000) 295
21. Lu W.G., Fang J.Y., Stokes K.L., and Lin J. J. Am. Chem. Soc. 126 (2004) 11798
22. Sootsman J.R., Pcionek R.J., Kong H., Uher C., and Kanatzidis M.G. Chem. Mater. 18 (2006) 4993
23. Hsu K.F., Loo S., Guo F., Chen W., Dyck J.S., Uher C., Hogan T., Polychroniadis E.K., and Kanatzidis M.G. Science 303 (2004) 818
24. Mokari T., Zhang M., and Yang P. J. Am. Chem. Soc. 129 (2007) 9864
25. Houtepen A.J., Koole R., Vanmaekelbergh D., Meeldijik J., and Hickey S.G. J. Am. Chem. Soc. 128 (2006) 6792
26. Steckel J.S., Yen B.K.H., Oertel D.C., and Bawendi M.G. J. Am. Chem. Soc. 128 (2006) 13032
27. Li C.R., Yao C.Z., Lu X.H., Zheng F.L., Feng Z.P., Yu X.L., Su C.Y., and Tong Y.X. Chem. Mater. 20 (2008) 3306
28. Abel K.A., Shan J., Boyer J.C., Harris F., and van Veggel F.C.J.M. Chem. Mater. 20 (2008) 3794
29. Law M., Luther J.M., Song Q., Hughes B.K., Perkins C.L., and Nozik A.J. J. Am. Chem. Soc. 130 (2008) 5974
30. Trindade T., O'Brien P., and Pickett N.L. Chem. Mater. 13 (2001) 3843
31. Sun J., and Buhro W.E. Angew. Chem. Int., Ed. Engl. 47 (2008) 3215
32. Trindade T., O'Brien P., Zhang X., and Motevalli M. J. Mater. Chem. 7 (1997) 1011
33. Dey S., Jain V.K., Chaudhury S., Knoedler A., and Kaim W. Polyhedron 22 (2003) 489
34. Kedarnath G., Dey S., Jain V.K., Dey G.K., and Varghese B. Polyhedron 25 (2006) 2383
35. Dey S., Jain V.K., Chaudhury S., Knoedler A., Lissner F., and Kaim W. J. Chem. Soc., Dalton Trans. (2001) 723
36. Kumbhare L.B., Jain V.K., Phadnis P.P., and Nethaji M. J. Organomet. Chem. 692 (2007) 1546
37. T. Higashi, ABSCOR-Empirical Absorption Correction based on Fourier Series Approximation, Rigaku Corporation, 3-9-12 Matsubara, Akishima, Japan, 1995.
38. G.M. Sheldrick, shelxs-97, Structure Solution Package, Universität Göttingen, Göttingen, Germany, 1997.
39. G.M. Sheldrick, shelxs-97, Structure Refinement Package, Universität Göttingen, Göttingen, Germany, 1997.
40. Liu C.W., Lobana T.S., Xiao J.L., Liu H.Y., Liaw B.J., Hung C.M., and Lin Z. Organometallics 24 (2005) 4072
41. Shimoni L., Glusker J.P., and Bock C.P. Inorg. Chem. 37 (1998) 1853
42. Hancock R.D., Reibenpies J.P., and Maumela H. Inorg. Chem. 43 (2004) 2981
43. JCPDS File No. 78-1901.
44. JCPDS File No. 78-1903.
45. B.D. Cullity, in: Elements of X-ray diffraction, Addison Wesley Inc., London, 1978.
46. Weller H. Angew. Chem., Int. Ed. Engl. 32 (1993) 41
47. Chen O., Chen Y., Yang Y., Lynch J., Wu H., Zhuang J., and Cao Y.C. Angew. Chem., Int. Ed. Engl. 47 (2008) 8638