The Malaysian Journal of Analytical Sciences Vol 12 No 1 (2008): 245 –
250
KAJIAN
KRISTALOGRAFI SINAR-X KOMPLEKS [µ-1(2-PIRIDIL-κN) ETANON 4-
FENILTIOUREASEMIKARBAZONATO-κ2N1, S] BIS[IODOMERKURI(II)] DAN BIS(N-4-METOKSIBENZOIL) -N’-O-TOLILTIOUREA-κS) DIIODOMERKURI(II)
Mohd Sukeri Mohd Yusof1
& Bohari M. Yamin2
1Jabatan
Sains Kimia, Fakulti Sains dan Teknologi Malaysia,
Universiti Malaysia Terengganu,t, 21030 K. Terengganu.
2Pusat Pengajian Sains Kimia
dan Teknologi Makanan, Fakulti Sains dan Teknologi,
Universiti Kebangsaan Malaysia,
43650 Bangi, Selangor.
Abstract
Both [µ-1(2-pyridyl-κN)ethanone
4-phenylthioureasemicarbazonato-κ2N1,S]bis[iodomercury(II)], and Bis(N-4 methoxybenzoyl)-N’-o-tolylthiourea-κS)diiodomercury(II), complexes have the molecular formula
of Hg2(L)2I2
and Hg(L)2I2 where L is the ligand,
respectively. They
also crystallized in monoclinic system,
but
having space group
is
C2/c,
a=18.466(3)Å, b=16.745(2)Å, c=13.9140(19)Å, β=129.174(2)º and P21/c, a=10.848(3)Å,
b=24.474(7)Å,
c=14.038(4)Å,
β=92.206(4)º, respectively. In the first complex, the Schiff base ligands are coordinated
to the mercury atom via their (NNS)
donor atoms in a tridentate manner.
The sulfur atoms act as a bridge connecting the Hg atoms, forming a rectangular base that
almost perpendicular to the ligand planes, resulting
in an open box-like structure. The geometry of the mercury atom is close to a square pyramid. However, the mercury atom in the mercury-thiourea complex is coordinated to the ligands via the thiono
sulfur atoms in a monodentate manner and form a distorted tetrahedral geometry.
Keywords: mercury complex, thiourea, benzoylthiourea
References
1. Olkhovyk,
O., Antochshuk, V., &
Jaroniec, M. 2004.
Benzoylthiourea-modified MCM-48 mesoporous
silica for mercury(II) adsorption from aqueous solutions.
Colloids and Surfaces A: Physicochemical and Engineering Aspect. Vol. 236, 1-3:69-72.
2. Rether,
A. & Schuster,
M. 2003. Selective
separation and recovery
of heavy metal
ions using water-soluble
N- benzoylthiourea modified PAMAM
polymers. Reactive and Functional Polymers, Vol. 57, 1:13-21.
3. Yusof,
M. S. M. & Yamin, B. M. 2004. N-Benzoyl-N’-(2-chlorophenyl)thiourea.
Acta Cryst. E60: 1403-1404.
4. Popovic,
Z., Pavlovic, G., Matkovic, D., Soldin, Z., Rajic, M., Vikic, D., & Kovacek, D. 2000. Mercury(II)
complexes of heterocyclic thiones.: Part 1. Preparation of 1:2 complexes of mercury(II)
halides and pseudohalides with 3,4,5,6-tetrahydropyrimidine-2-thione. X-ray, thermal
analysis and NMR studies. Inorganica Chimica Acta, Vol. 306: Issue 2:142-152.
5. Yusof,
M. S. M., Yamin, B. M. & Kassim, M. B. 2004. Bis(o-chlorophenylbenzoyl
thiourea- S)diiodomercury(II). Acta Cryst.
E60: m98-m99.
![]()
6. Leßmann,
F., Beyer, L., & Sieler, J. 2000. Synthesis and X-ray structure of the first
chloro-bridged thiourea mercury(II) complex [C6H5C(OCH3)NC(S)N(C2H5)2HgCl2]2. Inorganic
Chemistry Communications. Vol 3: Issue 2:62-64.
7. Yusof,
M. S. M., Yamin, B. M. & Shamsuddin M.
2003. N-(N-Benzoylhydrazino carbothioyl)benzamide. Acta Cryst.
E59: o810-o811.
8. Allen,
F.H., Kennard, O., Watson, D.G., Orpen, A.G. & Taylor, R. 1987. J. Chem.
Soc. Perkin Trans. 2:S1-19.
9. Orpen,
A.G., Brammer, L., Allen, F.H., Kennard,
O., Watson, D.G., & Taylor, R. 1989. J. Chem. Soc. Dalton Trans. S1-83.