Addition of 2-aminobenzothiazole and substituted derivatives to mercuric acetate in warm ethanol leads to the high yield formation of [Hg{SC6H3XN(C[triple bond, length as m-dash]N)}]n resulting from loss of hydrogen and sulfur-carbon bond cleavage. Addition of phosphines affords a series of complexes in which the new ortho-cyano-aminothiophenolate ligands adopt three different binding modes.

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Addition of 2-aminobenzothiazole (abt) and substituted derivatives to Hg(OAc)2 leads to the high yield formation of ortho-cyano-aminothiophenolate (ocap) complexes [Hg{SC6H3XN(C≡N)}]n (X = H, Me, Cl, Br, NO2) resulting from dehydrogenation...

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Three novel palladium­(II) mixed-ligand complexes of N-(benzothiazol-2-yl)­benzamide (HL) and 1,2-bis­(diphenylphosphino)­ethane (dppe), [Pd­(HL)­(dppe)]­Cl2 (1), [Pd­(L)­(dppe)]­Cl (2), and [Pd­(L)2(dppe)] (3), were synthesized and fully characterized using Fourier transform infrared, 1H, 13C, and 31P NMR, and molar conductivity measurements. Complex 3 was characterized by single-crystal X-ray diffraction. The ligand HL showed three different coordination modes: a neutral bidentate chelate bound through the endocyclic nitrogen and exocyclic oxygen atoms in 1, a negatively charged L bound as a bidentate chelate through the endocyclic nitrogen and negatively charged exocyclic oxygen atoms in 2, and a monodentate bound through the negatively charged endocyclic nitrogen atom in 3.

A series of Pd(II) complexes containing ortho-cyano-aminothiophenolate (ocap) ligands have been prepared and their molecular structures elucidated. Hg(II) ocap complexes, [Hg{SC6H3XN(C≡N)}]n (X = H, Me) (1), react with Na2S to...

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Reaction of cadimium(II) chloride CdCl2.6H2O with two equivalents of N-hydroxymethylsaccharin (Sac-CH2OH) (1) in the presence of NEt3 afforded the presumably tetrahedral complex [Cd(K2-Sac-CH2O)2] (2). The Sac-CH2O- ligand behaves as a bidentate chelate. Reaction of (2) with one equivalent of the bidentate ligands (dipos);  Ph2P(CH2)nPPh2, (n = 1 dppm; 2 dppe; 3 dppp; 4 dppb), Ph2P(S)(CH2)P(S)Ph2 (dppmS2)  afforded tetrahedral complexes of the type [Cd(K1-Sac-CH2O)2(diphos)] (3-7). The reaction with two equivalents of the monodentate ligands (phos); Ph3P or Ph3PS gave [Cd(K1-Sac-CH2O)2(phos)2] (8,9). The N-hydroxymethylsaccharinate anion acts as a monodentate ligand to the cadmium center through the hydroxymethyl oxygen atom. The complexes were characterized by physico-chemical and spectroscopic methods.