Skip to content
BY-NC-ND 3.0 license Open Access Published by De Gruyter Open Access August 11, 2008

Synthesis and structural peculiarities of gallium Complexes with novel paullone derivatives

  • Werner Ginzinger EMAIL logo , Vladimir Arion , Gerald Giester , Markus Galanski and Bernhard Keppler
From the journal Open Chemistry

Abstract

9-Bromo-7,12-dihydroindolo[3,2-d][1]benzazepin-6-ylhydrazine was reacted with 2-acetylpyridine to give a Schiff base as a potential tridentate ligand. The reaction of this ligand with gallium chloride afforded complexes of 1:1 and 2:1 stoichiometry. The results of X-ray diffraction studies of the ligand and both gallium complexes are reported and compared with the data for a related gallium complex with a Schiff base obtained from 9-bromo-7,12-dihydroindolo[3,2-d][1]benzazepin-6-ylhydrazine and 2-hydroxybenzaldehyde.

[1] D.W. Zaharevitz, R. Gussio, M. Leost, A.M. Senderowicz, T. Lahusen, C. Kunick, L. Meijer, E.A. Sausville, Cancer Res. 59, 2566 (1999). Search in Google Scholar

[2] E.B. Skibo, X. Huang, R. Martinez, R.H. Lemus, W.A. Craigo, J. Med. Chem. 55, 5543 (2002). http://dx.doi.org/10.1021/jm020285l10.1021/jm020285lSearch in Google Scholar

[3] C. Schultz, A. Link, M. Leost, D.W. Zaharevitz, R. Gussio, E.A. Sausville, L. Meijer, Kunick, J. Med. Chem. 42, 2909 (1999). http://dx.doi.org/10.1021/jm990057010.1021/jm9900570Search in Google Scholar

[4] J. Trapp, A. Jochum, R. Meier, L. Saunders, B. Marshall C. Kunick, E. Verdin, P. Goekjian, W. Sippl, M. Jung, J. Med. Chem. 49, 7307 (2006) http://dx.doi.org/10.1021/jm060118b10.1021/jm060118bSearch in Google Scholar

[5] W.F. Schmid, S. Zorbas-Seifried, R.O. John, V.B. Arion, M.A. Jakupec, A. Roller, M. Galanski, I. Chiorescu, H. Zorbas, B.K. Keppler, Inorg. Chem. 46, 3645 (2007). http://dx.doi.org/10.1021/ic070098j10.1021/ic070098jSearch in Google Scholar

[6] W.F. Schmid, R.O. John, G. Muehlgassner, P. Heffeter, M.A. Jakupec, M. Galanski, W. Berger, V.B. Arion, B.K. Keppler, J. Med. Chem. 50, 6343 (2007). http://dx.doi.org/10.1021/jm701042w10.1021/jm701042wSearch in Google Scholar

[7] A. Dobrov, V.B. Arion, N. Kandler, W. Ginzinger, M.A. Jakupec, A. Rufinska, N. Graf von Keyserlingk, M. Galanski, C. Kowol, B.K. Keppler, Inorg. Chem. 45, 1945 (2006). http://dx.doi.org/10.1021/ic051112010.1021/ic0511120Search in Google Scholar

[8] Z. Otwinowski, W. Minor, In: C.W. Carter Jr., R.M. Sweet, (Eds.), Methods in Enzymology Vol. 276: Macromolecular Crystallography Part A (Academic Press, London, 1997), 307 http://dx.doi.org/10.1016/S0076-6879(97)76066-X10.1016/S0076-6879(97)76066-XSearch in Google Scholar

[9] G.M. Sheldrick, SHELXS-97, Program for Crystal Structure Solution, University of Goettingen, Goettingen (1997) Search in Google Scholar

[10] Sheldrick G. M., SHELXL-97, Program for Crystal Structure Refinement, University of Goettingen, Goettingen (1997) Search in Google Scholar

[11] A.J.C. Wilson (Ed.), International Tables for X-ray Crystallography Vol. C (Kluwer Academic Publishers, Dordrecht, 1992), Tables 4.2.6.8 and 6.1.1.4 Search in Google Scholar

[12] A.L. Spek, J. Appl. Cryst. 36, 7 (2003). http://dx.doi.org/10.1107/S002188980202211210.1107/S0021889802022112Search in Google Scholar

[13] Bruker, XP (Version 5.1), Bruker AXS Inc., Madison, Wisconsin, USA (1998) Search in Google Scholar

[14] A.W. Addison, T.N. Rao, J. Reedijk, J. van Rijn, G.C. Verschoor, J. Chem. Soc. Dalton Trans. 7, 1349 (1984). http://dx.doi.org/10.1039/dt984000134910.1039/DT9840001349Search in Google Scholar

[15] K. Robinson, G.V. Gibbs, P.H. Ribbe, Science 172, 567 (1971). http://dx.doi.org/10.1126/science.172.3983.56710.1126/science.172.3983.567Search in Google Scholar PubMed

Published Online: 2008-8-11
Published in Print: 2008-9-1

© 2008 Versita Warsaw

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Downloaded on 1.5.2024 from https://www.degruyter.com/document/doi/10.2478/s11532-008-0048-x/html
Scroll to top button