Binuclear complexes of Pt(II) with platinated 2-phenylbenzothiazole and bridged derivatives of pyridin- and benzothiazol-2-thiols

Binuclear complexes of Pt(II) cycloplatinated with 2-phenylbenzothiazole and bridging ligands have been shown to contain the Pt-Pt bond. The complexes have been studied by X-ray diffraction, ¹H NMR and electronic absorption spectroscopy, and electrochemical methods. The complexes cis-N_(bt),S-isomers with antisymmetric positions of the cyclometalated and the bridging ligands have been detected in the crystals as well as in the solutions. The low-wavelength absorption and luminescence of the complexes have been assigned to the metal-metal-ligand charge transfer. The two-electron oxidation and reduction waves in the voltamperograms are associated with the metal- and the ligand-centered processes, respectively.     

Cyclopalladized complexes based on 2-phenylbenzothiazole

Russian Journal of General Chemistry -     

Synthesis and Properties of Platinum(II) 2-(2-Pyridyl)thiophenide Complexes and Ruthenium(II) Bisbipyridyl Complexes with 1,2-Bis(diphenylphosphino)ethene

Russian Journal of General Chemistry -     

Cyclopalladized complexes on the matrix of phenyland naphthyl-derivatives of oxazole and oxazoline with ethylenediamine

Russian Journal of General Chemistry -     

Preparation and Properties of Cyclopalladated Complexes of Dibenzo[a,c]phenazine and Dibenzo[f,h]quinoxaline with Ethylenediamine

Russian Journal of General Chemistry -     

Effect of acidification on spectral parameters of solutions of mixed-ligand cyclometalated Pt(II) and Pd(II) complexes

The effect of acidification of water-ethanol solutions of cyclometalated Pt(II) and Pd(II) complexes with ethylenediamine and cyanide ligands is studied. It is found that, unlike the ethylenediamine complexes, the cyclometalated complexes with cyanide ligands are unstable and undergo irreversible decyclometalation.     

Synthesis and Properties of Pd(II) and Pt(II) Cyanide Complexes with Cyclometalating Ligands Derived from 2-Phenylpyridine and 2-(2-Thienyl)pyridine

Russian Journal of General Chemistry -     

Study of ultrathin iron silicide films grown by solid phase epitaxy on the Si(001) surface

Ultrathin films of iron silicide have been grown by high-temperature annealing of 0.14-to O.5O-nm-thick Fe films deposited on the Si(001) surface at room temperature. It has been found that annealing leads to the formation of nanoislands of iron silicide on the surface, so that their type depends on the thickness of the Fe film. High-energy electron diffraction and atomic force microscopy measurements have revealed that the deposition of Fe films less than 0.32 nm thick on the Si(001) surface stimulates epitaxial growth of both three-dimensional β-FeSi₂ and two-dimensional γ-FeSi₂ islands. It has been found that, for Fe coverages of more than 0.32 nm thick, a complete transition to solide phase epitaxy is observed only for two-dimensional β-FeSi₂ islands. The effect of prolonged annealing at 850°C on the morphology of the surface of the iron silicide film has been investigated.     

Optical and spectroscopic properties of substituted oxa- and thiazole luminophores metalated with platinum metals

The cyclometalated [M(pbo)En]PF₆(M = Pd(II), Pt(II)), [M(pbo)₂En]PF₆ (M = Rh(III), Ir(III)), and [Rh(C∧N)₂En]PF₆ ((C∧N)^? are the deprotonated forms of 2-phenylbenzoxazole (pbo), 2,5-diphenyloxazole (dpo), 2-phenylbenzothiazole (pbt), 2-biphenyl-4-yl-5-phenyloxazole (bpo), and 2-biphenyl-4-yl-6-phenylbenzoxazole (bpbo) and En is ethylenediamine) complexes are studied by ¹H NMR spectroscopy, IR spectroscopy, and electronic absorption and emission spectroscopy. Metalation of luminophores leads to the formation of five-membered {M(C∧N)} cycles in the composition of plane-square and octahedral complexes of the cis-C,C structure. In addition to the intraligand (IL) π-π* optical transitions in the UV region, the complexes are characterized by long-wavelength metal-to-ligand charge-transfer (MLCT) absorption bands in the region of 366–416 nm. The phosphorescence of the complexes in the visible region (482–531 nm) is attributed to radiative transition from the mixed IL/MLCT electronically excited state. The temperature quenching of the phosphorescence of complexes is attributed to the thermally activated population of metal-centered electronically excited states with subsequent nonradiative deactivation.