Room-temperature emission from platinum(II) complexes intercalated into zirconium phosphate-layered materials.
Room-temperature emission from platinum(II) complexes intercalated into zirconium phosphate-layered materials.
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DOI:
10.1021/ic7006183
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发表时间:
2007-09
影响因子:
4.6
通讯作者:
Eladio J. Rivera;C. Figueroa;J. Colón;L. Grove;W. Connick
中科院分区:
文献类型:
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作者:
Eladio J. Rivera;C. Figueroa;J. Colón;L. Grove;W. Connick
The direct ion exchange of chloro(2,6-bis(N-methylbenzimidazol-2-yl)pyridine)platinum(II) ([Pt(Me(2)bzimpy)Cl]+) and chloro(2,2':6',2' '-terpyridine)platinum(II) ([Pt(tpy)Cl]+) complexes within a zirconium phosphate (ZrP) framework has been accomplished. The physical and spectroscopic properties of [Pt(Me(2)bzimpy)Cl]+ and [Pt(tpy)Cl]+ intercalated in ZrP were investigated by X-ray powder diffraction and X-ray photoelectron, infrared, absorption, and luminescence spectroscopies. In contrast to unintercalated complexes in fluid solution, which do not emit at room temperature, both intercalated materials in the solid state and in colloidal suspensions exhibit intense emissions at room temperature. A [Pt(Me(2)bzimpy)Cl]+-exchanged ZrP colloidal methanol suspension gives rise to an emission at 612 nm that originates from a lowest (3)MMLCT[dsigma*(Pt) --> pi*(tpy)] state (MMLCT = metal-metal-to-ligand charge transfer) characteristic of strong Pt...Pt interactions. A [Pt(tpy)Cl]+-exchanged ZrP colloidal aqueous suspension exhibits a strong emission band at 600 nm. The accumulated data demonstrate that at high concentrations, [Pt(Me(2)bzimpy)Cl]+ and [Pt(tpy)Cl]+ ions can serve as luminescent pillars inside the ZrP framework.