2-imino-4-oxo-1,3-thiazolidine complexes of silver(I), zinc(II), cadmium(II) and mercury(II)
TL;DR: In this article, the infrared spectral studies suggest that silver and zinc derivatives are N-bonded, cadmium complex is S-Bonded and mercury derivatives are both N- and S-bunded.
Abstract: Complexes of the types [MXL2], [MXL2L2] and [MX2L] (where M = AgI, ZNII, CdII or HgII; X =Cl, Br, I, SCN, NO3, ClO4 or 1 2 SO4; L =2-imino-4-oxo-1,3-thiazolidine) have been prepared as white, diamagnetic non-electrolyte compounds. The infrared spectral studies suggest that silver and zinc derivatives are N-bonded, cadmium complex is S-bonded and mercury derivatives are both N- and S-bonded.
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TL;DR: In this paper, the perchlorate ion complexes have been studied and the metal-perchlorate bond has been termed as "semicoordination" and has been shown to be weak.
Abstract: Publisher Summary This chapter discusses the perchlorate ion complexes. Coordination of perchlorate to transition and nontransition metal ions has been well established, though in most of the cases the metal-perchlorate bond is rather weak and has been termed as “semicoordination”. The highly symmetrical perchlorate ion is a hard base and falls into the category of relatively nonpolarizable and noncoordinating anions such as BF 4 ˉ and PF 6 ˉ. Its ability to coordinate strongly to soft metal ions is therefore limited. When coordination does occur, the perchlorate group may be linked to a metal ion in a monodentate and/or bidentate manner through oxygen atoms; the latter linkage can be either chelating. X-ray crystal structure analysis has unequivocally established coordination of perchlorate in a number of perchlorate complexes.
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TL;DR: In this paper, the infrared spectra of the solid complexes and of 1H nuclear magnetic resonance spectra were compared, and it was shown that 2J(1H199Hg) indicates bonding to sulfur only.
Abstract: The novel complexes RHg(s2UraH−1) (R = Me, Ph) where s2UraH−1 is the monoanion of 2-thiouracil, have been synthesized. Comparison of the infrared spectra of the solid complexes and of 1H nuclear magnetic resonance spectra of the complexes in dimethyl-d6 sulfoxide with spectra of s2 Ura and Na[s2UraH−1] allows the recognition of the existence of isomers in the solid, with bonding to exocyclic sulfur and to pyrimidine nitrogens. In solution, a simpler pattern is observed, with 2J(1H199Hg) indicating bonding to sulfur only.
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TL;DR: Palladium(II) and platinum (II) halides with 3,6-disubstituted 2,7-dihydro-1,4,5-thiadiazepine derivatives (L) form complexes of general formula as discussed by the authors.
Abstract: Palladium(II) and platinum(II) halides with 3,6-disubstituted-2,7-dihydro-1,4,5-thiadiazepine derivatives (L) form complexes of general formula, [MX 2 ·L′] (L′ = monohydrazone, VII). During the formation of these complexes, the thiadiazepine ring underwent hydrolytic cleavage at the carbon- nitrogen double bond, the nitrogen of which is involved in coordination with the metal ions These complexes have also been obtained from mono. hydrozones of 2,2″-thiodiacetophenones. These are diamagnetic and non-electrolytes. From their it, n.m.r., electronic spectra, T.G.A., D.T.A., magnetic susceptibility and conductivity measurements, these complexes have been assigned a square planar structure.
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TL;DR: In this article, Ubersicht uber Strukturen und Spektren von festen Quecksilberhalogeniden und ihren Solvaten is presented, together with solvaten.
Abstract: Review: Ubersicht uber Strukturen und Spektren von festen Quecksilberhalogeniden und ihren Solvaten.
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