Preparation and Properties of Gadolinium Homoleptic Double-and Triple-Decker Complexes Containing Tetrabenzoporphyrin Ligand

Article Preview

Abstract:

Two novel gadolinium sandwich-type complexes containing tetrabenzoporphyrin (TBP) ligands-Gd (TBP)2 and Gd (TBP)3 were prepared from porphyrin 1 and Gd (acac)3. nH2O under Ar by boiling 1, 2, 4-Tcb for 15~17h and 45~48 h respectively. Their structures are characterized by Uv-Vis, HR-MS and IR. The spectroscopic studies show that their longest-wavelength visible and near-IR absorption bands are obviously red-shifted due to the extension of the π conjugated systems in the TBP ring. The magnetic studies indicate that the observed value of χMT for Gd (TBP)2 is close to the combined value of Gd (III) and porphyrin radical anion at room temperature and that antiferromagnetic interaction possibly results from the intramolecular spin exchange between the porphyrin π-radical electron and that the gadolinium f unpaired electrons dominates its magnetic properties over the whole temperature range while there is no magnetic interactions between two Gd (III) ions in Gd (TBP)3 in the range from room temperature down to 20K and very weak antiferromagnetic coupling exsits between two Gd (III) ions below 20K.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 750-752)

Pages:

1816-1821

Citation:

Online since:

August 2013

Authors:

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Buchler J W, Kapellmann H G, Knoff M, et al. Z. Naturforsch., Teil B, 1983, 38, 1339-1345.

Google Scholar

[2] Jiang J, Ng D K P. Acc. Chem. Res., 2009, 42, 79-88.

Google Scholar

[3] Goransson E, Boixel J, Monnereau C, et al. Inorg. Chem., 2010, 49, 9823-9832.

Google Scholar

[4] Tsikalas G, Coutsolelos A G. Inorg. Chem., 2003, 42, 6801-6804.

Google Scholar

[5] Spyroulias G A, Raptopoulou C P, De Montauzon D, et al. Inorg. Chem., 1999, 38, 1683-1696.

Google Scholar

[6] Otsuki J, Kawaguchi S, Yamakawa T, et al. Langmuir, 2006, 22, 5708-5715.

Google Scholar

[7] Ito S, Murashima T, Ono N. J. Chem. Soc. Perkin Trans. 1., 1997, 21, 3161-3166.

Google Scholar

[8] Wong C P, Venteicher R F, Horrcks W, et al. J. Am. Chem. Soc., 1974, 96, 4149-4151.

Google Scholar

[9] Ito S, Murashima T, Ono N. J. Chem. Soc. Perkin Trans. I, 1997, 3161-3165.

Google Scholar

[10] Bisel O, Rodriguez J, Milam S N, et al. J. Am. Chem. Soc., 1992, 114, 6528-6538.

Google Scholar

[11] Bilsel O, Rodriguez J, Holten D. J. Phys. Chem., 1990, 94, 3508-3512.

Google Scholar

[12] Wittmer L L, Holten D. J. Phys. Chem., 1996, 100, 860-868.

Google Scholar

[13] Lau R L C, Jiang J, Ng D K P, et al. J. Am. Soc. Mass Spectrom., 1997, 8, 161-169.

Google Scholar

[14] Shimomura E T, Phillippi M A, Goff H M. J. Am. Chem. Soc., 1981, 103, 6778-6780.

Google Scholar

[15] Collman J P, Kendall J K, Chen J L, et al. Inorg. Chem., 2000, 39, 1661-1667.

Google Scholar