Structure, optical and electrochemical properties of binuclear complexes with platinated 2-phenylbenzothiazol and bridging 2-mercapto-derivatives of pyridine, pyrimidine, benzothiazole, and benzoxazole

Standard

Structure, optical and electrochemical properties of binuclear complexes with platinated 2-phenylbenzothiazol and bridging 2-mercapto-derivatives of pyridine, pyrimidine, benzothiazole, and benzoxazole. / Katlenok, E.A.; Zolotarev, A.A.; Ivanov, A.Yu.; Smirnov, S.N.; Balashev, K.P.

In: Journal of Structural Chemistry, No. 5, 2015, p. 880-886.

Research output: Contribution to journal › Article

BibTeX

@article{0f1faf36499b41f2b005a70ac9ee6fab,

title = "Structure, optical and electrochemical properties of binuclear complexes with platinated 2-phenylbenzothiazol and bridging 2-mercapto-derivatives of pyridine, pyrimidine, benzothiazole, and benzoxazole",

abstract = "{\textcopyright} 2015 Pleiades Publishing, Ltd.Binuclear [Pt(bt)μ-(N^S)]2 complexes (bt-is the deprotonated form of 2-phenylbenzothiazole, (N^S)- = 2- mercaptopyridineate, 2-mercaptopyrimidineate, 2-mercaptobenzothiazoleate, 2-mercaptobenzoxazoleate ions) are characterized by the following methods: X-ray crystallography, 1H and 195Pt NMR spectroscopy, electronic absorption and emission spectroscopy, cyclic voltammetry. The occurrence of the Pt-Pt chemical bond and complexes in both crystalline state and solution in the form of cis-N(bt),S-binding isomers with the asymmetrical arrangement of two cyclometalated and two bridging ligands is shown. Long-wave absorption bands and luminescence of the complexes in the red spectral range are due to spin-allowed and spin-forbidden optical charge transfer transitions from the metal-metal bond to the metalated ligand. In cyclic voltammetry, two-electron redox waves of the complexes are attributed to metal- and ligand-centered processes involving σ∗HOMO and π∗(bt) LUMO of the complexes.",

author = "E.A. Katlenok and A.A. Zolotarev and A.Yu. Ivanov and S.N. Smirnov and K.P. Balashev",

year = "2015",

doi = "10.1134/S0022476615050091",

language = "English",

pages = "880--886",

journal = "Journal of Structural Chemistry",

issn = "0022-4766",

publisher = "Springer Nature",

number = "5",

}

RIS

TY - JOUR

T1 - Structure, optical and electrochemical properties of binuclear complexes with platinated 2-phenylbenzothiazol and bridging 2-mercapto-derivatives of pyridine, pyrimidine, benzothiazole, and benzoxazole

AU - Katlenok, E.A.

AU - Zolotarev, A.A.

AU - Ivanov, A.Yu.

AU - Smirnov, S.N.

AU - Balashev, K.P.

PY - 2015

Y1 - 2015

N2 - © 2015 Pleiades Publishing, Ltd.Binuclear [Pt(bt)μ-(N^S)]2 complexes (bt-is the deprotonated form of 2-phenylbenzothiazole, (N^S)- = 2- mercaptopyridineate, 2-mercaptopyrimidineate, 2-mercaptobenzothiazoleate, 2-mercaptobenzoxazoleate ions) are characterized by the following methods: X-ray crystallography, 1H and 195Pt NMR spectroscopy, electronic absorption and emission spectroscopy, cyclic voltammetry. The occurrence of the Pt-Pt chemical bond and complexes in both crystalline state and solution in the form of cis-N(bt),S-binding isomers with the asymmetrical arrangement of two cyclometalated and two bridging ligands is shown. Long-wave absorption bands and luminescence of the complexes in the red spectral range are due to spin-allowed and spin-forbidden optical charge transfer transitions from the metal-metal bond to the metalated ligand. In cyclic voltammetry, two-electron redox waves of the complexes are attributed to metal- and ligand-centered processes involving σ∗HOMO and π∗(bt) LUMO of the complexes.

AB - © 2015 Pleiades Publishing, Ltd.Binuclear [Pt(bt)μ-(N^S)]2 complexes (bt-is the deprotonated form of 2-phenylbenzothiazole, (N^S)- = 2- mercaptopyridineate, 2-mercaptopyrimidineate, 2-mercaptobenzothiazoleate, 2-mercaptobenzoxazoleate ions) are characterized by the following methods: X-ray crystallography, 1H and 195Pt NMR spectroscopy, electronic absorption and emission spectroscopy, cyclic voltammetry. The occurrence of the Pt-Pt chemical bond and complexes in both crystalline state and solution in the form of cis-N(bt),S-binding isomers with the asymmetrical arrangement of two cyclometalated and two bridging ligands is shown. Long-wave absorption bands and luminescence of the complexes in the red spectral range are due to spin-allowed and spin-forbidden optical charge transfer transitions from the metal-metal bond to the metalated ligand. In cyclic voltammetry, two-electron redox waves of the complexes are attributed to metal- and ligand-centered processes involving σ∗HOMO and π∗(bt) LUMO of the complexes.

U2 - 10.1134/S0022476615050091

DO - 10.1134/S0022476615050091

M3 - Article

SP - 880

EP - 886

JO - Journal of Structural Chemistry

JF - Journal of Structural Chemistry

SN - 0022-4766

IS - 5

ER -

ID: 4003761