“…Notably, on examination of literature only two examples of metal-h 1 -tellurophene coordination were found; these examples were of rhodium(III) bound to dibenzotelluro- phene and the sum of angles around tellurium were 2978 and 305,8 compared to 2768 for 5-PdCl 2 . [26] The 1 H NMR spectrum of 5-PdCl 2 (Figure 2) is fully consistent with the solid-state structure of this complex, in terms of the number of resonances, which indicate nonequivalency of all hydrogen atoms. The side-on coordination of palladium causes differentiation of signals of meso-phenyl substituents, observed below 280 K. The proton chemical shifts that are characteristic of porphyrins and the characteristic pattern of the UV/Vis electronic spectrum, which contains an intense Soret-like band at 442 and 493 nm, (Figure 3) are consistent with 5-PdCl 2 having macrocyclic aromaticity.…”
Pd verdrängt Te: Ein Palladacyclopentadien wurde in ein Porphyrinoidgerüst eingebaut. Bei der Koordination von Palladium(II) in einem 21,23‐Ditelluraporphyrin kam es zum Austausch eines Tellur‐ gegen das Palladiumatom unter Bildung des aromatischen 21‐Pallada‐23‐telluraporphyrins. Das nichtplanare Molekül liegt im Gleichgewicht zweier asymmetrischer Formen vor.
“…Notably, on examination of literature only two examples of metal-h 1 -tellurophene coordination were found; these examples were of rhodium(III) bound to dibenzotelluro- phene and the sum of angles around tellurium were 2978 and 305,8 compared to 2768 for 5-PdCl 2 . [26] The 1 H NMR spectrum of 5-PdCl 2 (Figure 2) is fully consistent with the solid-state structure of this complex, in terms of the number of resonances, which indicate nonequivalency of all hydrogen atoms. The side-on coordination of palladium causes differentiation of signals of meso-phenyl substituents, observed below 280 K. The proton chemical shifts that are characteristic of porphyrins and the characteristic pattern of the UV/Vis electronic spectrum, which contains an intense Soret-like band at 442 and 493 nm, (Figure 3) are consistent with 5-PdCl 2 having macrocyclic aromaticity.…”
Pd verdrängt Te: Ein Palladacyclopentadien wurde in ein Porphyrinoidgerüst eingebaut. Bei der Koordination von Palladium(II) in einem 21,23‐Ditelluraporphyrin kam es zum Austausch eines Tellur‐ gegen das Palladiumatom unter Bildung des aromatischen 21‐Pallada‐23‐telluraporphyrins. Das nichtplanare Molekül liegt im Gleichgewicht zweier asymmetrischer Formen vor.
“…9 The reactions of monodentate heterocyclic organotellurium ligands with the pentamethylcyclopentadienylrhodium() dichloride dimer have also been reported as potential models for the initial steps in heterogeneously catalysed hydrodesulfurisation. 10,11 However the preparation of organometallic complexes with seleno-or telluro-ether ligands is generally limited to carbonyl containing species.…”
“…The [PdCl 2 (tellurocyclpentane) 2 ] is the first complex of tellurocyclopentane to be characterized structurally 4 . McWhinnie and his coworkers 4,5 have studied the reactions of Te heterocycles with Fe 3 (CO) 12, and [{Rh(η 5 -C 5 Me 5 )Cl 2 }] very recently. The detelluration of Te-heterocycles is a common feature of these reactions.…”
The palladium(II) and platinum(II) complexes of 1,4-oxatellurane (L), having the composition [MCl2L2], are synthesized and characterized spectroscopically and structurally (Pt complex only; Pt–Cl 2.3169(9) Å; Pt–Te 2.5945(3) Å) for the first time.
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