Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical called Bridge-splitting reactions and far infrared spectra of diene derivatives of palladium(II) and platinum(II) complexes, Author is Crociani, Bruno; Uguagliati, Paolo; Boschi, Tristano; Belluco, Umberto, which mentions a compound: 12266-72-7, SMILESS is I[Pt]I.C1=CCC/C=CCC/1, Molecular C8H12I2Pt, Related Products of 12266-72-7.
Bridge-splitting reactions of complexes of the type [M(diene.OMe)X]2 (M = Pd(II), Pt(II); diene = cycloocta-1,5-diene, dicyclopentadiene; X = Cl, Br) by neutral ligands (L) having N or P as donor atoms are reported. For the products [M(diene.OMe)LX] two structures are possible, i.e., with L cis to the olefinic double bond (A) or trans to it (B). On the basis of far-ir, spectra, structure (A) has been attributed to [Pd(diene.OMe)(py)Cl] and [Pt(diene.-OMe)LX)] (L = pyridine and p-toluidine). Structure (B) has been attributed to [Pt(diene.OMe)(PPh3)X] and to the analogous Pd(II) complexes. From [M(diene.OMe)(py)Cl] the pyridine is displaced by another neutral ligand, whereas the chloride ion is displaced only by an anionic one. The far-ir spectra (500-60 cm.-1) of the dimers [M(diene.OMe)X]2 are reported and the metal-bridging halogen stretching frequencies are assigned on the basis of a Cipoint-group symmetry. The v(M-Clbridging) falls in the range 298-216 cm.-1, v(M-Brbridging 201-148 cm.-1, and v(M-Ibridging) 165-122 cm.-1
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Reference:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics