Rhodium (III) analogues of antitumour-active ruthenium(III) compounds: The crystal structure of [ImH] [trans-RhCl4(Im)2] (Im = imidazole)

  • Mestroni G.
  • Alessio E.
  • Sessanta O Santi A.
  • Geremia S.
  • Bergamo A.
  • Sava G.
  • Boccarelli A.
  • Schettino A.
  • Coluccia M.
Publication date
January 1998
Publisher
Elsevier BV

Abstract

A series of neutral and anionic Rh(III)-chloride compounds bearing ammonia or imidazole (Im) ligands, and isostructural to Ru(III) complexes endowed with antineopiastic activity, were synthesized and characterized spectroscopically. The X-ray crystal structure of [ImH] [trans-RhCl4(Im)2] was determined. Crystal data: monoclinic, space group C2/c, Z = 4, a = 13.133(3), b = 7.977(1), c = 16.683(4) Å, β = 113.84(2)°. The solution behaviour and some biological parameters of the new rhodium compounds, including cytotoxicity, in vitro interactions with DNA and in vivo antitumour activity against a tumour model, were investigated and compared with those of the corresponding ruthenium analogues. © 1998 Elsevier Science S.A. All rights reserved

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