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Inorganics 2014, 2(3), 508-523; https://doi.org/10.3390/inorganics2030508

Half-Lantern Pt(II) and Pt(III) Complexes. New Cyclometalated Platinum Derivatives

1
Departamento de Química Inorgánica, Escuela de Ingeniería y Arquitectura de Zaragoza, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), CSIC—Universidad de Zaragoza, Edificio Torres Quevedo, Campus Río Ebro, Zaragoza 50018, Spain
2
Departamento de Química Inorgánica, Facultad de Ciencias, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), CSIC—Universidad de Zaragoza, Pedro Cerbuna 12, Zaragoza 50009, Spain
*
Author to whom correspondence should be addressed.
Received: 7 July 2014 / Revised: 4 August 2014 / Accepted: 5 August 2014 / Published: 26 August 2014
(This article belongs to the Special Issue Organoplatinum Complexes)
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Abstract

The divalent complex [{Pt(bzq)(μ-L)}2] (1) [Hbzq = benzo[h]quinolone, HL = CF3C4H2N2SH: 4-(trifluoromethyl)pyrimidine-2-thiol] was obtained from equimolar amounts of [Pt(bzq)(NCMe)2]ClO4 and 4-(trifluoromethyl)pyrimidine-2-thiol with an excess of NEt3. The presence of a low intensity absorption band at 486 nm (CH2Cl2), assignable to a metal-metal-to-ligand charge transfer transition (1MMLCT) [dσ*(Pt)2→π*(bzq)], is indicative of the existence of two platinum centers located in close proximity because the rigidity of the half-lantern structure allows the preservation of these interactions in solution. Compound 1 undergoes two-electron oxidation upon treatment with halogens X2 (X2: Cl2, Br2 or I2) to give the corresponding dihalodiplatinum (III) complexes [{Pt(bzq)(μ-L)X}2] (L = CF3C4H2N2S-κN,S; X: Cl 2, Br 3, I 4). Complexes 24 were also obtained by reaction of 1 with HX (molar ratio 1:2, 10% excess of HX) in THF with yields of about 80% and compound 2 was also obtained by reaction of [{Pt(bzq)(μ-Cl)}2] with HL (4-(trifluoromethyl)pyrimidine-2-thiol) in molar ratio 1:2 in THF, although in small yield. The X-ray structures of 2 and 3 confirmed the half-lantern structure and the anti configuration of the molecules. Both of them show Pt–Pt distances (2.61188(15) Å 2, 2.61767(16) Å 3) in the low range of those observed in Pt2(III,III)X2 half-lantern complexes. View Full-Text
Keywords: half-lantern compounds; cyclometalated; platinum (II); platinum (III) half-lantern compounds; cyclometalated; platinum (II); platinum (III)
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Sicilia, V.; Borja, P.; Martín, A. Half-Lantern Pt(II) and Pt(III) Complexes. New Cyclometalated Platinum Derivatives. Inorganics 2014, 2, 508-523.

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