TAUTOMERIC CONVERSION OF A THIOUREA LIGAND UPON FORMATION OF A HYPERVALENT TELLURIUM(II) COMPLEX - SYNTHESIS, AND X-RAY STRUCTURAL STUDIES OF N-PHENYL-N'-(1,3-THIAZOL-2-YL)-THIOUREA AND BROMOPHENYL HIAZOL-3'-IUM-2'-YL)-ISOTHIOUREIDATO]TELLURIUM(II)
Md. Rudd et al., TAUTOMERIC CONVERSION OF A THIOUREA LIGAND UPON FORMATION OF A HYPERVALENT TELLURIUM(II) COMPLEX - SYNTHESIS, AND X-RAY STRUCTURAL STUDIES OF N-PHENYL-N'-(1,3-THIAZOL-2-YL)-THIOUREA AND BROMOPHENYL HIAZOL-3'-IUM-2'-YL)-ISOTHIOUREIDATO]TELLURIUM(II), Phosphorus, sulfur and silicon and the related elements, 123, 1997, pp. 313-327
The divalent tellurium title complex (II) has been synthesized by addi
tion of Ph2Te2 and Br-2 to the ligand 1-phenyl-3-(2-thiazolyl)-2-thiou
rea (I). The molecular structures of I and II were subsequently determ
ined by X-ray crystallographic methods. As a result, it was found that
upon complexation, the ligand had undergone a transition from a thiou
rea to to an isomeric isothiourea, involving a transfer of a thiourea
proton to the thiazolyl ring. This does not seem to influence the bond
ing properties of the ligand, and the reasons for this are discussed.
The central tellurium atom is three-coordinate and its coordination sp
here is T-shaped with a linear S-Te-Br sequence with bond lengths Te(1
)-S(1) and Te(1)-Br(1) equal to 2.548(1) and 2.883(1) Angstrom, respec
tively, and angle S(1)-Te(1)-Br(1)=174.49(2)degrees. At nearly right a
ngles to this sequence, there is a Te(1)-C(11)(phenyl) bond of 2.127(3
) Angstrom.