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Title: Dipyridocatecholate-bridged complexes of platinum and ruthenium diimine chromophores

Journal Article · · Inorganic Chemistry
DOI:https://doi.org/10.1021/ic971447k· OSTI ID:653425
; ;  [1]
  1. Univ. of Rochester, NY (United States). Dept. of Chemistry

New Ru-Pt heterometallic complexes have been prepared and their electrochemical and luminescence properties characterized. One series of complexes contains a tris diimine-chelated Ru(II) center linked to one, two, or three Pt(II) diimine moieties via a dipyridocatecholate (dpcat; 1,10-phenanthroline-5,6-diolate) bridging ligand, as indicated by the general formula [(dbbpy){sub 3{minus}n}Ru(({micro}-dpcat)Pt(dbbpy)){sub n}](PF{sub 6}){sub 2} (n = 1--3) where dbbpy = di-tert-butylbipyridine. A different dinuclear complex has a tetrapyridophenazine (tppz) bridge connecting a Ru(diimine){sub 3}{sup 2+} chromophore with a Pt diimine dithiolate center and has the formula [(dbbpy){sub 2}Ru({mu}-tppz)Pt(tdt)]{sup 2+} where tdt = toluene-3,4-dithiolate. The dpcat-bridged complexes exhibit numerous redox processes that are assigned on the basis of comparison of those shown by mononuclear precursors and analogues, i.e., Ru(diimine){sub 3}{sup 2+} and Pt(dbbpy)(dpcat). The dpcat-bridged complexes display distinct absorption bands due to Ru(diimine){sub 3}{sup 2+} and Pt(diimine)(diolate) chromophores at ca. 450 and 540 nm, respectively. Emission from the Pt center is observed at 77 K upon direct irradiation of this center as well as excitation of the Ru center. In contrast the mononuclear complex Pt(dbbpy)(dpcat) does not luminescence, even in rigid media at low temperature.

Sponsoring Organization:
USDOE, Washington, DC (United States)
OSTI ID:
653425
Journal Information:
Inorganic Chemistry, Vol. 37, Issue 16; Other Information: PBD: 10 Aug 1998
Country of Publication:
United States
Language:
English