Synthesis of five new molybdenum(VI) thiosemicarbazonato complexes. Crystal structures of salicylaldehyde and 3-methoxy-salicylaldehyde 4-methylthiosemicarbazones and their molybdenum(VI) complexes

被引:72
作者
Vrdojak, V
Cindric, M
Milic, D
Matkovic-Calogovic, D
Novak, P
Kamenar, B
机构
[1] Univ Zagreb, Fac Sci, Dept Chem, Lab Gen & Inorgan Chem, Zagreb 10000, Croatia
[2] Univ Zagreb, Fac Sci, Dept Chem, Analyt Chem Lab, Zagreb 10000, Croatia
关键词
molybdenum(VI) complexes; thiosemicarbazones; mononuclear and polynuclear complexes; tridentate ligands; crystal structures;
D O I
10.1016/j.poly.2005.05.002
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Polynuclear [MoO2{SalTSC-4-Me}](n) (1), [MoO2{VanTSC-4-Me}](n) (II) and mononuclear [MoO2{SaITSC-4-Me}(CH3OH)] (1a), [MoO2{VanTSC-4-Me}(CH3OH)] (2a) and [MoO2{VanTSC-4-Me}(H2O)]center dot CH3CN (2b) complexes have been prepared by the reaction of the [MoO2(acac)(2)] (acetylacetonate ligand, acac(-), C5H7O2-) with 1 (salicylaldehyde 4-methylthiosemicarbazone ligand, C6H4(OH)CH:NNC(SH)NHCH3, H(2)VanTSC-4-Me) or 2 (3-methoxy-salicylaidehyde 4-methylthiosemicarbazone, CH3OC6H3(OH)CH:NNQSH)NHCH3, H2VanTSC-4-Me) in acetonitrile or in dry methanol. All complexes have been characterized by means of chemical analyses, thermogravimetric analyses, IR spectroscopy and some of them by H-1, C-13 NMR spectroscopy and X-ray crystallography. In all mononuclear complexes molybdenum atom is coordinated by two terminal oxo-oxygen atoms, by ONS atoms from the ligand molecule and by an oxygen atom from methanol (in 1a and 2a) or water (in 2b) molecules. Ligands 1 and 2 have been characterized by means of H-1, C-13 NMR spectroscopy and X-ray crystallography. Molecules of both ligands are found to be in the thioketo tautomeric form. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1717 / 1726
页数:10
相关论文
共 43 条
[1]   Appended 1,2-naphthoquinones as anticancer agents 1: synthesis, structural, spectral and antitumor activities of ortho-naphthaquinone thiosemicarbazone and its transition metal complexes [J].
Afrasiabi, Z ;
Sinn, E ;
Chen, JN ;
Ma, YF ;
Rheingold, AL ;
Zakharov, LN ;
Rath, N ;
Padhye, S .
INORGANICA CHIMICA ACTA, 2004, 357 (01) :271-278
[2]  
ALI MA, 1974, COORDIN CHEM REV, V13, P101
[3]   Transition metal complexes with thiosemicarbazide-based ligands .25. Synthesis and x-ray crystal structure of cis-dioxo [(salicylaldehyde thiosemicarbazonato(1-))] aquomolybdenum (VI) chloride monohydrate, [MoO2(HL)H2O]Cl.H2O [J].
Argay, G ;
Kalman, A ;
Leovac, VM ;
Cesljevic, VI ;
Ribar, B .
JOURNAL OF COORDINATION CHEMISTRY, 1996, 37 (1-4) :165-171
[4]   LEAST-SQUARES ABSOLUTE-STRUCTURE REFINEMENT - PRACTICAL EXPERIENCE AND ANCILLARY CALCULATIONS [J].
BERNARDINELLI, G ;
FLACK, HD .
ACTA CRYSTALLOGRAPHICA SECTION A, 1985, 41 (SEP) :500-511
[5]   Four cytotoxic N4-substituted thiosemicarbazones derived from 2-hydroxynaphthalene-1-carboxaidehyde [J].
Bernhardt, PV ;
Caldwell, LM ;
Lovejoy, DB ;
Richardson, DR .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 2003, 59 :O629-O633
[6]  
BHATTACHARYA PK, 1990, P INDIAN AS-CHEM SCI, V102, P247
[7]   CONFORMATION OF 6-MEMBERED RINGS [J].
BOEYENS, JCA .
JOURNAL OF CRYSTAL AND MOLECULAR STRUCTURE, 1978, 8 (06) :317-320
[8]   CRYSTAL AND MOLECULAR STRUCTURE OF BENZIL BISTHIOSEMICARBAZONATOCOPPER(II) AND THE ANTI-TUMOR MECHANISM OF RELATED COMPOUNDS [J].
BUSHNELL, GW ;
TSANG, AYM .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1979, 57 (06) :603-607
[9]   SYNTHESIS, CHARACTERIZATION, AND ELECTROCHEMISTRY OF CIS-DIOXOMOLYBDENUM(VI) COMPLEXES OF SCHIFF-BASES DERIVED FROM CARBOHYDRAZIDE, THIOCARBOHYDRAZIDE, AND SALICYLALDEHYDE - CRYSTAL-STRUCTURES OF [MOO2(O-OC6H4CH=NN=CSNHN=CHC6H4OH-O)ME2SO] AND [(MOO2)2(O-OC6H4CH=NN=CONN=CHC6H4O-O)(ME2SO)2].0.5ME2SO [J].
BUSTOS, C ;
BURCKHARDT, O ;
SCHREBLER, R ;
CARRILLO, D ;
ARIF, AM ;
COWLEY, AH ;
NUNN, CM .
INORGANIC CHEMISTRY, 1990, 29 (20) :3996-4001
[10]   STRUCTURE OF SALICYLALDEHYDE THIOSEMICARBAZONE [J].
CHATTOPADHYAY, D ;
MAZUMDAR, SK ;
BANERJEE, T ;
GHOSH, S ;
MAK, TCW .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1988, 44 :1025-1028